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Iijima Kazutmo  飯島 一誠

… Alternative Names

IIJIMA Kazumoto  飯島 一誠

NOZU Kandai  野津 寛大

KAITO Hiroshi  貝藤 裕史

HARA Shigeo  原 重雄

飯島 一誠  イイジマ カヅモト

Less
Researcher Number 00240854
Other IDs
  • ORCIDhttps://orcid.org/0000-0001-9846-4142
Affiliation (Current) 2025: 神戸大学, 医学研究科, 客員教授
Affiliation (based on the past Project Information) *help 2020 – 2024: 神戸大学, 医学研究科, 客員教授
2016 – 2020: 神戸大学, 医学研究科, 教授
2017: 神戸大学, 大学院医学研究科, 教授
2017: 神戸大学, 大学院医学研究科内科系講座小児化学分野, 教授
2011 – 2016: 神戸大学, 医学(系)研究科(研究院), 教授 … More
2015: 神戸大学, 大学院医学研究科, 准教授
2015: 神戸大学, 大学院医学研究科, 助教
2015: 神戸大学, 大学院医学研究科, 教授
2015: 神戸大学, 大学院医学研究科, 講師
2014: 神戸大学, 大学院医学研究科・内科系講座小児科, 教授
2009 – 2011: 神戸大学, 医学部, 教授
2010: 神戸大学, 医学研究科, 教授
2010: Kobe University, 大学院・医学研究科, 教授
2008 – 2009: Kobe University, 医学研究科, 特命教授
2006 – 2007: 国立成育医療センター(研究所), 腎臓科, 医長
2005: 国立成育医療センター(研究所), 小児腎臓科, 医長
2005: National Center for Child Health and Development, Director, 小児腎臓科, 医長
1996 – 1999: Kobe University School of Medicine, Assistant, 医学部, 助手
1995: 神戸大学, 医学部・附属病院, 助手
1993: 神戸大学, 医学部・付属病院, 助手 Less
Review Section/Research Field
Principal Investigator
Kidney internal medicine / Basic Section 53040:Nephrology-related / Medium-sized Section 53:Organ-based internal medicine and related fields / Kidney internal medicine
Except Principal Investigator
Pediatrics / Kidney internal medicine / Kidney internal medicine
Keywords
Principal Investigator
小児ネフローゼ症候群 / ネフローゼ症候群 / 抗ネフリン抗体 / ネフリン / 疾患感受性遺伝子 / 腎臓学 / 遺伝子 / エクソンスキッピング / アルポート症候群 / 原因遺伝子 … More / メサンギウム細胞 / 血管透過性亢進因子 / リツキシマブ / GWASメタ解析 / 腎臓オルガノイド / iPS細胞 / 器官システム内科学 / フィンランド型先天性ネフローゼ症候群 / ゲノムワイド関連解析 / ステロイド感受性ネフローゼ症候群 / 重症化機序 / Genetics / Familial / Nephrotic Syndrome / 家族性 / Mesangial proliferative glomerulonephritis / alpha-smooth muscle actin / Mesangial cells / Renal biopsy specimen / Vascular endothelial growth factor / Vascular permeability factor / α-smooth muscle actin / 腎生検組織 / α-Smooth muscle achin / メサンギウム増殖性腎炎 / α-Smooth muscle actin / 腎生検 / 血管内皮細胞増殖因子 / 医療・福祉 / アンチセンスオリゴヌクレオチド / 分子治療 / 腎尿路奇形 / 多嚢胞性異形成腎(MCDK) / TCF2 / genome-wide CNV array / copy number variation(CNV) / microduplication / microdeletion / copy number variation (CNV) / 先天性腎尿路奇形(CAKUT) / CNV解析 / 先天性腎尿路奇形 / mRNA / デキサメサゾン / phorbol ester / TGF-beta / 末梢血単核球 … More
Except Principal Investigator
次世代シークエンサー / ネフローゼ症候群 / 遺伝子変異 / mutations / 診断 / 修飾遺伝子 / 高い診断能力 / 体細胞モザイク / 網羅的遺伝子解析 / Alport症候群 / NPHP-RC / 遺伝カウンセリング / 繊毛病 / 先天性腎尿路異常 / ネフロン癆 / 嚢胞性腎疾患 / 小児CKD / CAKUT / ベロ毒素 / 尿細管培養細胞 / サイトカイン / アポトーシス / 志賀毒素 / 溶血性尿毒症症候群 / 嚢胞性線維症 / 遺伝性クロル下痢症 / 遺伝性高カルシウム尿性低カルシウム血症 / ターゲットシークエンス / 遺伝性塩類喪失性尿細管機能異常症 / 遺伝性低マグネシウム血症 / Copy number variation / 遺伝性尿細管機能異常症 / ギッテルマン症候群 / バーター症候群 / 塩類喪失性尿細管機能異常症 / linkage analysis / mutation / podocytes / nephrotic syndrome / 連鎖解析 / ポドサイト / gene mutation / Platelet-activating factor acetylhydrolase / Platelet-activating factor / relapse / steroid-responsive nephrotic syndrome / Japanese children / 分解酵素 / 血小板活性化因子 / mRNA / direct sequence / RT-PCR / COL4A5 / type IV collagen alpha5 chain / glomerular basement membrane / X-linked Alport syndrome / IV型コラーゲン / エフソン / IV型コラーゲンα5鎖 / 遺伝子 / アルポート症候群 / 小児腎臓病学 / ナンセンスリードスルー / エクソンスキッピング / ナンセンスリードスルー療法 / 遺伝性腎疾患 / マイクロサテライトマーカー / 乳児ネフローゼ症候群 / 先天性ネフローゼ症候群 / PLEC1 / ラミニンβ2 / WT1 / ポドシン / ネフリン Less
  • Research Projects

    (20 results)
  • Research Products

    (605 results)
  • Co-Researchers

    (29 People)
  •  Elucidation of the mechanism of rituximab-induced long-term remission in childhood nephrotic syndromePrincipal Investigator

    • Principal Investigator
      飯島 一誠
    • Project Period (FY)
      2023 – 2025
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Review Section
      Basic Section 53040:Nephrology-related
    • Research Institution
      Kobe University
  •  Joint international Research Project for International GWAS Meta-Analysis and Anti-Nephrin Autoantibodies in Childhood Nephrotic SyndromePrincipal Investigator

    • Principal Investigator
      Iijima Kazumoto
    • Project Period (FY)
      2021 – 2023
    • Research Category
      Fund for the Promotion of Joint International Research (Fostering Joint International Research (B))
    • Review Section
      Medium-sized Section 53:Organ-based internal medicine and related fields
    • Research Institution
      Kobe University
  •  Clarification of the pathogenesis of childhood nephrotic syndrome using iPS cell-derived kidney organoidsPrincipal Investigator

    • Principal Investigator
      Iijima Kazumoto
    • Project Period (FY)
      2020 – 2022
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Review Section
      Basic Section 53040:Nephrology-related
    • Research Institution
      Kobe University
  •  Joint International Research for identification of disease-susceptible genes and drug-sensitive genes in childhood nephrotic syndromePrincipal Investigator

    • Principal Investigator
      IIJIMA KAZUMOTO
    • Project Period (FY)
      2018 – 2020
    • Research Category
      Fund for the Promotion of Joint International Research (Fostering Joint International Research (B))
    • Review Section
      Medium-sized Section 53:Organ-based internal medicine and related fields
    • Research Institution
      Kobe University
  •  Identification of Genes Involved in the Severity of Alport Syndrome and Elucidation of the Mechanism of its SeverityPrincipal Investigator

    • Principal Investigator
      Iijima Kazumoto
    • Project Period (FY)
      2017 – 2019
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Kidney internal medicine
    • Research Institution
      Kobe University
  •  Establishment of a comprehensive diagnostic method using next generation sequencer for Alport syndrome

    • Principal Investigator
      Yamamura Tomohiko
    • Project Period (FY)
      2016 – 2017
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  The onset mechanisms for inherited salt-losing tubulopathies

    • Principal Investigator
      Nozu Kandai
    • Project Period (FY)
      2015 – 2017
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Identification of new causative gene for congenital anomalies of the kidney and urinary tract (CAKUT) and elucidation for pathology of CAKUT by iPS cells

    • Principal Investigator
      Morisada Naoya
    • Project Period (FY)
      2015 – 2017
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Kidney internal medicine
    • Research Institution
      Kobe University
  •  Development of molecular therapy for Alport syndromePrincipal Investigator

    • Principal Investigator
      Iijima Kazumoto
    • Project Period (FY)
      2014 – 2017
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Kidney internal medicine
    • Research Institution
      Kobe University
  •  Nonsense read-through therapy for Aport syndrome

    • Principal Investigator
      KANDAI Nozu
    • Project Period (FY)
      2013 – 2014
    • Research Category
      Grant-in-Aid for Research Activity Start-up
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  The investigation for mechanism of tubular injury with diarrhea associated hemolytic uremic syndrome

    • Principal Investigator
      Takeshi Ninchoji
    • Project Period (FY)
      2013 – 2015
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  New responsible genes for CAKUT and development of comprehensive gene mutation detection system in CAKUTPrincipal Investigator

    • Principal Investigator
      IIJIMA Kazumoto
    • Project Period (FY)
      2011 – 2013
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Kidney internal medicine
    • Research Institution
      Kobe University
  •  Mutation analysis in Japanese patients with congenital and infantile nephritic syndrome

    • Principal Investigator
      YOSHIKAWA Norishige
    • Project Period (FY)
      2009 – 2011
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Wakayama Medical University
  •  Identification of novel genes for congenital anomalies of Kidney and urinary tract (CAKUT) by CNV analyses and development of comprehensive gene testing for CAKUTPrincipal Investigator

    • Principal Investigator
      IIJIMA Kazumoto
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Kidney internal medicine
    • Research Institution
      Kobe University
  •  Analysis of familial steroid-sensitive nephrotic syndromePrincipal Investigator

    • Principal Investigator
      IIJIMA Kazumoto
    • Project Period (FY)
      2006 – 2007
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Kidney internal medicine
    • Research Institution
      National Research Institute for Child Health and Development
  •  Gene Mapping for Familial Steroid Resistance Nephritic Syndrome

    • Principal Investigator
      TSUKAGUCHI Hiroyasu
    • Project Period (FY)
      2004 – 2005
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Kidney internal medicine
    • Research Institution
      The University of Tokushima
  •  Platelet-activating factor acetylhydrolase gene mutation in Japanese nephrotic children.

    • Principal Investigator
      YOSHIKAWA Norishige
    • Project Period (FY)
      1999 – 2000
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Kidney internal medicine
    • Research Institution
      Kobe University
  •  The roles of vascular permeability factor/vascular endothelial growth factor in mesangial proliferative glomerulonephritisPrincipal Investigator

    • Principal Investigator
      IIJIMA Kazumoto
    • Project Period (FY)
      1996 – 1997
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Kidney internal medicine
    • Research Institution
      Kobe University
  •  X-linked Alport syndrome : Mutation survey over all 51 exons of the COL4A5 gene

    • Principal Investigator
      YOSHIKAWA Norishige
    • Project Period (FY)
      1995 – 1996
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Kidney internal medicine
    • Research Institution
      Kobe University
  •  血管透過性亢進因子と尿蛋白発現に関する研究Principal Investigator

    • Principal Investigator
      飯島 一誠
    • Project Period (FY)
      1993
    • Research Category
      Grant-in-Aid for Encouragement of Young Scientists (A)
    • Research Field
      Kidney internal medicine
    • Research Institution
      Kobe University

All 2024 2023 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006 2005 Other

All Journal Article Presentation Book

  • [Book] ネフローゼ症候群(ステロイド感受性)小児科診療ガイドライン-最新の診療指針-第3版 (編集:五十嵐隆)2016

    • Author(s)
      飯島一誠
    • Total Pages
      670
    • Publisher
      総合医学社
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Book] 腎と透析【多発性嚢胞腎-基礎と臨床のトピックス】 臨床 遺伝カウンセリングの実際2016

    • Author(s)
      森貞直哉、飯島一誠
    • Total Pages
      1080
    • Publisher
      東京医学社
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Book] 腎臓内科・泌尿器科 CAKUT2016

    • Author(s)
      森貞直哉、飯島一誠
    • Total Pages
      114
    • Publisher
      科学評論社
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Book] 小児疾患診療のための病態生理2 改訂5版2015

    • Author(s)
      森貞直哉、飯島一誠
    • Total Pages
      1120
    • Publisher
      東京医学社
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Book] 12.Bartter症候群、Gitelman症候群2015

    • Author(s)
      野津寛大
    • Total Pages
      629
    • Publisher
      医学書院
    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Book] Alport症候群の軽症亜型 Annual Review 2015腎臓2015

    • Author(s)
      野津寛大、飯島一誠
    • Total Pages
      230
    • Publisher
      中外医学社
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Book] 先天代謝異常ハンドブック2013

    • Author(s)
      飯島一誠
    • Publisher
      中山書店
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Book] 今日の治療指針 2012年版2012

    • Author(s)
      飯島一誠
    • Publisher
      医学書院
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Book] 特発性ネフローゼ症候群 小児腎臓病学2012

    • Author(s)
      飯島一誠
    • Publisher
      診断と治療社
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Book] 小児腎臓病学2012

    • Author(s)
      飯島一誠
    • Publisher
      診断と治療社
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Book] 最新ガイドライン準処 小児科診断・治療指針2012

    • Author(s)
      飯島一誠
    • Publisher
      中山書店
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Book] 2011-2012EBM小児疾患の治療(五十嵐隆, 石井正浩, 清水俊明, 滝田順子, 平岩幹男, 水口雅, 横田俊平, 横谷進, 渡辺とよ子編)(小児ステロイド抵抗性ネフローゼ症候群に対するリツキシマブの効果は?)2011

    • Author(s)
      飯島一誠, 貝藤裕史, 伊藤秀一
    • Publisher
      中外医学社
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Book] 微小変化型ネフローゼ症候群:小児『2011-2013腎疾患・透析最新の治療』(槙野博史,秋沢忠男編)2011

    • Author(s)
      飯島一誠
    • Publisher
      南江堂
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Book] 微小変化型ネフローゼ症候群:小児 2011-2013 腎疾患・透析 最新の治療2011

    • Author(s)
      飯島一誠
    • Publisher
      南江堂
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Book] 小児ステロイド抵抗性ネフローゼ症候群に対するリツキシマブの効果は? 2011-2012 EBM小児疾患の治療2011

    • Author(s)
      飯島一誠,貝藤裕史,伊藤秀一
    • Publisher
      中外医学社
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Book] 小児ネフローゼ症候群の新たな治療 Annual Review腎臓20112011

    • Author(s)
      飯島一誠,佐古まゆみ
    • Publisher
      中外医学社
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Book] III.Clinical nephrology A.糸球体障害 小児ネフローゼ症候群の新たな治療『Annual Review腎臓2011』(富野康日己, 柏原直樹, 成田一衛編)2011

    • Author(s)
      飯島一誠, 佐古まゆみ
    • Publisher
      中外医学社
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Book] Annual Review腎臓2010小児科領域TCF2遺伝子異常と先天性腎尿路奇形.(御手洗哲也, 東原英二, 秋澤忠男, 五十嵐隆, 金井好克編)2010

    • Author(s)
      中山真紀子, 野津寛大, 飯島一誠
    • Publisher
      中外医学社
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Book] 講義録 小児科学:微小変化型ネフローゼ症候群、巣状糸球体硬化症、遺伝性腎症2008

    • Author(s)
      飯島 一誠
    • Total Pages
      789
    • Publisher
      メジカルレビュー社
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Book] 講義録小児科学:微小変化型ネフローゼ症候群、巣状糸球体硬化症、遺伝性腎症2008

    • Author(s)
      飯島 一誠
    • Total Pages
      789
    • Publisher
      メジカルレビュー社
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Book] 小児疾患診療のための病態生理 ステロイド抵抗性ネフローゼ症候群2008

    • Author(s)
      飯島一誠
    • Total Pages
      1573
    • Publisher
      東京医学社
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Book] 小児科学 第3版:爪膝蓋骨症候群、Fabry病、ネフロン労2008

    • Author(s)
      飯島 一誠
    • Total Pages
      1855
    • Publisher
      医学書院
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Book] 小児科学第3版:爪膝蓋骨症候群、Fabry病、ネフロン労2008

    • Author(s)
      飯島 一誠
    • Total Pages
      1855
    • Publisher
      医学書院
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Book] 小児科学第3版 爪膝蓋骨症候群、Fabry病、ネフロン労2008

    • Author(s)
      飯島一誠
    • Total Pages
      1855
    • Publisher
      医学書院
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 【腎臓学この1年の進歩】ネフリンとネフローゼ症候群2024

    • Author(s)
      飯島 一誠, 堀之内 智子, 長野 智那, 野津 寛大
    • Journal Title

      日本腎臓学会誌

      Volume: 66巻 Pages: 303-309

    • Data Source
      KAKENHI-PROJECT-21KK0147
  • [Journal Article] 【遺伝を考える】(II章)遺伝学的診断 個別診療分野における遺伝学的診断の進歩 腎・泌尿器領域2023

    • Author(s)
      飯島 一誠, 堀之内 智子, 野津 寛大
    • Journal Title

      日本医師会雑誌

      Volume: 152巻特別1

    • Data Source
      KAKENHI-PROJECT-21KK0147
  • [Journal Article] Rituximab in combination with cyclosporine and steroid pulse therapy for childhood-onset multidrug-resistant nephrotic syndrome: a multicenter single-arm clinical trial (JSKDC11 trial)2023

    • Author(s)
      Nozu Kandai、Sako Mayumi、Tanaka Seiji、Kano Yuji、Ohwada Yoko、Morohashi Tamaki、Hamada Riku、Ohtsuka Yasufumi、Oka Masafumi、Kamei Koichi、Inaba Aya、Ito Shuichi、Sakai Tomoyuki、Kaito Hiroshi、Shima Yuko et al.
    • Journal Title

      Clinical and Experimental Nephrology

      Volume: 28 Issue: 4 Pages: 337-348

    • DOI

      10.1007/s10157-023-02431-0

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-23K07300, KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-23K27617
  • [Journal Article] 特集 病因・病態生理から読み解く腎・泌尿器疾患のすべて Ⅱ.糸球体疾患 1.微小変化型ネフローゼ症候群2023

    • Author(s)
      飯島 一誠
    • Journal Title

      腎と透析

      Volume: 95 Issue: 7 Pages: 26-31

    • DOI

      10.24479/kd.0000000991

    • ISSN
      0385-2156
    • Year and Date
      2023-12-15
    • Data Source
      KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-23K27617
  • [Journal Article] 【遺伝を考える】(II章)遺伝学的診断 個別診療分野における遺伝学的診断の進歩 腎・泌尿器領域2023

    • Author(s)
      飯島 一誠, 堀之内 智子, 野津 寛大
    • Journal Title

      日本医師会雑誌

      Volume: 152巻特別1

    • Data Source
      KAKENHI-PROJECT-23K27617
  • [Journal Article] A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants2023

    • Author(s)
      Malakasioti G, Iancu D, Milovanova A, Tsygin A, Horinouchi T, Nagano C, Nozu K, Kamei K, Fujinaga S, Iijima K, et al. ; CNI in Monogenic SRNS Study Investigators
    • Journal Title

      Kidney International

      Volume: 103 Issue: 5 Pages: 962-972

    • DOI

      10.1016/j.kint.2023.02.022

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-20H03698
  • [Journal Article] Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome2023

    • Author(s)
      Barry A, McNulty MT, Jia X, Nagano C, Horinouchi T, Nozu K, Tokunaga K, Ronco P, Iijima K, Sampson MG, et al.
    • Journal Title

      Nature Communications

      Volume: 14 Issue: 1 Pages: 2481-2481

    • DOI

      10.1038/s41467-023-37985-w

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-23K27617
  • [Journal Article] Clinical, Pathological, and Genetic Characteristics in Patients with Focal Segmental Glomerulosclerosis2022

    • Author(s)
      Nagano C, Hara S, Yoshikawa N, Takeda A, Gotoh Y, Hamada R, Matsuoka K, Yamamoto M, Fujinaga S, Sakuraya K, Kamei K, Hamasaki Y, Oguchi H, Araki Y, Ogawa Y, Okamoto T, Ito S, Tanaka S, Kaito H, Aoto Y, Ishiko S, Rossanti R, Sakakibara N, Horinouchi T, Yamamura T, Nagase H, Iijima K, Nozu K
    • Journal Title

      Kidney360

      Volume: 3 Issue: 8 Pages: 1384-1393

    • DOI

      10.34067/kid.0000812022

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-20H03698
  • [Journal Article] An updated view of the pathogenesis of steroid-sensitive nephrotic syndrome2022

    • Author(s)
      Horinouchi Tomoko、Nozu Kandai、Iijima Kazumoto
    • Journal Title

      Pediatric Nephrology

      Volume: - Issue: 9 Pages: 1957-1965

    • DOI

      10.1007/s00467-021-05401-4

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-20H03698, KAKENHI-PROJECT-20K16892, KAKENHI-PROJECT-21KK0147
  • [Journal Article] Is influenza vaccination associated with nephrotic syndrome relapse in children? A multicenter prospective study2022

    • Author(s)
      Ishimori S, Horinouchi T, Fujimura J, Yamamura T, Matsunoshita N, Kamiyoshi N, Sato M, Ogura M, Kamei K, Ishikura K, Iijima K, Nozu K
    • Journal Title

      Pediatric Nephrology

      Volume: Nov 30 Issue: 7 Pages: 2107-2116

    • DOI

      10.1007/s00467-022-05783-z

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-20H03698
  • [Journal Article] An extremely mild clinical course in a case with LAMB2-associated nephritis diagnosed with next-generation sequencing.2021

    • Author(s)
      Sakuraya K, Nozu K, Murakami H, Nagano C, Horinouchi T, Fujinaga S, Iijima K, Ohtomo Y.
    • Journal Title

      CEN Case Reports

      Volume: - Issue: 3 Pages: 359-363

    • DOI

      10.1007/s13730-021-00574-1

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-19K08726
  • [Journal Article] FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a child.2021

    • Author(s)
      Rossanti R, Watanabe T, Nagano C, Hara S, Horinouchi T, Yamamura T, Sakakibara N, Ninchoji T, Iijima K, Nozu K.
    • Journal Title

      CEN Case Reports

      Volume: 10(1) Issue: 1 Pages: 100-105

    • DOI

      10.1007/s13730-020-00529-y

    • Open Access
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Journal Article] A Novel Truncating PAX2 Mutation in a Boy With Renal Coloboma Syndrome With Focal Segmental Glomerulosclerosis Causing Rapid Progression to End-Stage Kidney Disease2020

    • Author(s)
      Saida K, Kamei K, Morisada N, Ogura M, Ogata K, Matsuoka K, Nozu K, Iijima K, Ito S.
    • Journal Title

      CEN Case Rep

      Volume: 9 Issue: 1 Pages: 19-23

    • DOI

      10.1007/s13730-019-00419-y

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-18KK0244
  • [Journal Article] A cross-sectional nationwide survey of congenital and infantile nephrotic syndrome in Japan.2020

    • Author(s)
      Hamasaki Y, Hamada R, Muramatsu M, Matsumoto S, Aya K, Ishikura K, Kaneko T, Iijima K.
    • Journal Title

      BMC Nephrology

      Volume: 21(1) Issue: 1 Pages: 363-363

    • DOI

      10.1186/s12882-020-02010-5

    • Open Access
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Journal Article] Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome2020

    • Author(s)
      Jia Xiaoyuan、Yamamura Tomohiko、et al.
    • Journal Title

      Kidney International

      Volume: 98 Issue: 5 Pages: 1308-1322

    • DOI

      10.1016/j.kint.2020.05.029

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-20K08370, KAKENHI-PROJECT-20K16892, KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-20H03698
  • [Journal Article] Molecular mechanisms determining severity in patients with Pierson syndrome2020

    • Author(s)
      Minamikawa Shogo、Miwa Saori、Inagaki Tetsuji、Nishiyama Kei、Kaito Hiroshi、Ninchoji Takeshi、Yamamura Tomohiko、Nagano China、Sakakibara Nana、Ishimori Shingo、Hara Shigeo、Yoshikawa Norishige、Hirano Daishi、Harada Ryoko、Hamada Riku、Matsunoshita Natsuki、Nagata Michio、Shima Yuko、Nozu Kandai
    • Journal Title

      Journal of Human Genetics

      Volume: 65 Issue: 4 Pages: 355-362

    • DOI

      10.1038/s10038-019-0715-0

    • NAID

      120006811107

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-17K16087, KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-19K17297, KAKENHI-PROJECT-18KK0244
  • [Journal Article] Comprehensive genetic diagnosis of Japanese patients with severe proteinuria.2020

    • Author(s)
      Nagano C, Yamamura T, Horinouchi T, Aoto Y, Ishiko S, Sakakibara N, Shima Y, Nakanishi K, Nagase H, Iijima K, Nozu K.
    • Journal Title

      Sci Rep.

      Volume: 10(1) Issue: 1 Pages: 428-437

    • DOI

      10.1038/s41598-019-57149-5

    • NAID

      120006884200

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-18K15713
  • [Journal Article] Biallelic variants/mutations of IL1RAP in patients with steroid-sensitive nephrotic syndrome2019

    • Author(s)
      Niitsuma Sou、Kudo Hiroki、Kikuchi Atsuo、Hayashi Takaya、Kumakura Satoshi、Kobayashi Shuhei、Okuyama Yuko、Kumagai Naonori、Niihori Tetsuya、Aoki Yoko、So Takanori、Funayama Ryo、Nakayama Keiko、Shirota Matsuyuki、Kondo Shuji、Kagami Shoji、Tsukaguchi Hiroyasu、Iijima Kazumoto、Kure Shigeo、Ishii Naoto
    • Journal Title

      International Immunology

      Volume: 32 Issue: 4 Pages: 283-292

    • DOI

      10.1093/intimm/dxz081

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K09719, KAKENHI-PUBLICLY-18H04795, KAKENHI-PROJECT-17H04035, KAKENHI-PROJECT-18H02572, KAKENHI-PROJECT-17K08875, KAKENHI-PROJECT-18K19281, KAKENHI-PROJECT-19H03612, KAKENHI-PROJECT-18KK0244
  • [Journal Article] Establishment of X-linked Alport syndrome model mice with a Col4a5 R471X mutation2019

    • Author(s)
      Hashikami Kentarou、Asahina Makoto、Nozu Kandai、Iijima Kazumoto、Nagata Michio、Takeyama Michiyasu
    • Journal Title

      Biochemistry and Biophysics Reports

      Volume: 17 Pages: 81-86

    • DOI

      10.1016/j.bbrep.2018.12.003

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Journal Article] アルポート症候群2019

    • Author(s)
      野津寛大、飯島一誠
    • Journal Title

      指定難病ペディア,日本医師会雑誌

      Volume: 148 Pages: 249-249

    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Journal Article] Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay.2019

    • Author(s)
      Horinouchi T, Nozu K, Yamamura T, Minamikawa S, Nagano C, Sakakibara N, Nakanishi K, Shima Y, Morisada N, Ishiko S, Aoto Y, Nagase H, Takeda H, Rossanti R, Kaito H, Matsuo M, Iijima K.
    • Journal Title

      Sci Rep.

      Volume: 9(1) Issue: 1 Pages: 12696-12696

    • DOI

      10.1038/s41598-019-48990-9

    • NAID

      120006825910

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-18K15712
  • [Journal Article] Prognosis and acute complications at the first onset of idiopathic nephrotic syndrome in children: a nationwide survey in Japan (JP-SHINE study)2019

    • Author(s)
      Sato Mai、Ishikura Kenji、Ando Takashi、Kikunaga Kaori、Terano Chikako、Hamada Riku、Ishimori Shingo、Hamasaki Yuko、Araki Yoshinori、Gotoh Yoshimitsu、Nakanishi Koichi、Nakazato Hitoshi、Matsuyama Takeshi、Iijima Kazumoto、Yoshikawa Norishige、Ito Shuichi、Honda Masataka
    • Journal Title

      Nephrology Dialysis Transplantation

      Volume: - Issue: 3 Pages: 475-481

    • DOI

      10.1093/ndt/gfz185

    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Journal Article] Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome2019

    • Author(s)
      Rossanti Rini、Shono Akemi、Miura Kenichiro、Hattori Motoshi、Yamamura Tomohiko、Nakanishi Keita、Minamikawa Shogo、Fujimura Junya、Horinouchi Tomoko、Nagano China、Sakakibara Nana、Kaito Hiroshi、Nagase Hiroaki、Morisada Naoya、Asanuma Katsuhiko、Matsuo Masafumi、Nozu Kandai、Iijima Kazumoto
    • Journal Title

      Journal of Human Genetics

      Volume: 64 Issue: 7 Pages: 673-679

    • DOI

      10.1038/s10038-019-0606-4

    • NAID

      120006653286

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-19K09921, KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-18K15712, KAKENHI-PROJECT-18H02823
  • [Journal Article] Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome.2019

    • Author(s)
      Yamamura T, Nozu K, Minamikawa S, Horinouchi T, Sakakibara N, Nagano C, Aoto Y, Ishiko S, Nakanishi K, Shima Y, Nagase H, Rossanti R, Ye MJ, Nozu Y, Ishimori S, Morisada N, Kaito H, Iijima K.
    • Journal Title

      Mol Genet Genomic Med.

      Volume: 7(9) Issue: 9

    • DOI

      10.1002/mgg3.883

    • NAID

      120006733124

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-17H04189
  • [Journal Article] Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndrome2018

    • Author(s)
      Unzaki Ai、Morisada Naoya、Nozu Kandai、Ye Ming Juan et al
    • Journal Title

      Journal of Human Genetics

      Volume: 63 Issue: 5 Pages: 647-656

    • DOI

      10.1038/s10038-018-0429-8

    • NAID

      120006647352

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-17K09689, KAKENHI-PROJECT-18K08243
  • [Journal Article] Germline mosaicism is a pitfall in the diagnosis of “sporadic” X-linked Alport syndrome2018

    • Author(s)
      Okamoto Takayuki、Nozu Kandai、Iijima Kazumoto、Ariga Tadashi
    • Journal Title

      Journal of Nephrology

      Volume: 32 Issue: 1 Pages: 155-159

    • DOI

      10.1007/s40620-018-0518-y

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Journal Article] Study protocol: mycophenolate mofetil as maintenance therapy after rituximab treatment for childhood-onset, complicated, frequently-relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicenter double-blind, randomized, placebo-controlled trial (JSKDC07)2018

    • Author(s)
      Horinouchi Tomoko、Sako Mayumi、Nakanishi Koichi、Ishikura Kenji、Ito Shuichi、Nakamura Hidefumi、Oba Mari Saito、Nozu Kandai、Iijima Kazumoto
    • Journal Title

      BMC Nephrology

      Volume: 19 Issue: 1 Pages: 302-302

    • DOI

      10.1186/s12882-018-1099-7

    • NAID

      120006539303

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Journal Article] Study protocol: high-dose mizoribine with prednisolone therapy in short-term relapsing steroid-sensitive nephrotic syndrome to prevent frequent relapse (JSKDC05 trial).2018

    • Author(s)
      Hama T, Nakanishi K, Ishikura K, Ito S, Nakamura H, Sako M, Saito-Oba M, Nozu K, Shima Y, Iijima K, Yoshikawa N; Japanese Study Group of Kidney Disease in Children (JSKDC).
    • Journal Title

      BMC Nephrol.

      Volume: 19 Issue: 1 Pages: 223-223

    • DOI

      10.1186/s12882-018-1033-z

    • NAID

      120006523804

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-15K09694
  • [Journal Article] Long-term clinicopathologic observation in a case of steroid-resistant nephrotic syndrome caused by a novel Crumbs homolog 2 mutation.2018

    • Author(s)
      Watanabe S, Aizawa T, Tsukaguchi H, Tsugawa K, Tsuruga K, Shono A, Nozu K, Iijima K, Joh K, Tanaka H.
    • Journal Title

      Nephrology (Carlton)

      Volume: - Issue: 7 Pages: 697-702

    • DOI

      10.1111/nep.13244

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16K10055, KAKENHI-PROJECT-16K10066, KAKENHI-PROJECT-17K09719, KAKENHI-PROJECT-18KK0244
  • [Journal Article] Idiopathic nephrotic syndrome in children2018

    • Author(s)
      Noone Damien G、Iijima Kazumoto、Parekh Rulan
    • Journal Title

      The Lancet

      Volume: 392 Issue: 10141 Pages: 61-74

    • DOI

      10.1016/s0140-6736(18)30536-1

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Journal Article] A review of clinical characteristics and genetic backgrounds in Alport syndrome2018

    • Author(s)
      Nozu K, Nakanishi K, Abe Y, Udagawa T, Okada S, Okamoto T, Kaito H, Kanemoto K, Kobayashi A, Tanaka E, Tanaka K, Hama T, Fujimaru R, Miwa S, Yamamura T, Yamamura N, Horinouchi T, Minamikawa S, Nagata M, Iijima K
    • Journal Title

      Clinical and Experimental Nephrology

      Volume: 23 Issue: 2 Pages: 158-168

    • DOI

      10.1007/s10157-018-1629-4

    • NAID

      120006557458

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-17H06658
  • [Journal Article] Rituximab in steroid-sensitive nephrotic syndrome: lessons from clinical trials2018

    • Author(s)
      Iijima Kazumoto、Sako Mayumi、Kamei Koichi、Nozu Kandai
    • Journal Title

      Pediatric Nephrology

      Volume: 33 Issue: 9 Pages: 1449-1455

    • DOI

      10.1007/s00467-017-3746-9

    • NAID

      120006498201

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Journal Article] Homozygous splicing mutation in NUP133 causes Galloway-Mowat syndrome2018

    • Author(s)
      Fujita Atsushi、Tsukaguchi Hiroyasu、Koshimizu Eriko、Nakazato Hitoshi、Itoh Kyoko、Kuraoka Shohei、Komohara Yoshihiro、Shiina Masaaki、Nakamura Shohei、Kitajima Mika、Tsurusaki Yoshinori、Miyatake Satoko、Ogata Kazuhiro、Iijima Kazumoto、Matsumoto Naomichi、Miyake Noriko
    • Journal Title

      Annals of Neurology

      Volume: 84 Issue: 6 Pages: 814-828

    • DOI

      10.1002/ana.25370

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17K09719, KAKENHI-PROJECT-17K10080, KAKENHI-PROJECT-17K19536, KAKENHI-PROJECT-18K19305, KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-17H01539, KAKENHI-PROJECT-16H03293, KAKENHI-PROJECT-16H05357, KAKENHI-PROJECT-17H06994
  • [Journal Article] Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population.2018

    • Author(s)
      Jia X, Horinouchi T, Hitomi Y, Shono A, Khor SS, Omae Y, Kojima K, Kawai Y, Nagasaki M, Kaku Y, Okamoto T, Ohwada Y, Ohta K, Okuda Y, Fujimaru R, Hatae K, Kumagai N, Sawanobori E, Nakazato H, Ohtsuka Y, Nakanishi K, Shima Y, Tanaka R, Ashida A, Kamei K, Ishikura K, Nozu K, Tokunaga K, Iijima K
    • Journal Title

      J Am Soc Nephrol.

      Volume: 29 Issue: 8 Pages: 2189-2199

    • DOI

      10.1681/asn.2017080859

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18KK0244, KAKENHI-PLANNED-18H05511, KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-16K10066
  • [Journal Article] Ocular findings in a case of Pierson syndrome with a novel mutation in laminin ?2 gene2018

    • Author(s)
      Arima Mitsuru、Tsukamoto Shoko、Akiyama Rumi、Nishiyama Kei、Kohno Ri-ichiro、Tachibana Takashi、Hayashida Akira、Murayama Miwa、Hisatomi Toshio、Nozu Kandai、Iijima Kazumoto、Ohga Shouichi、Sonoda Koh-Hei
    • Journal Title

      Journal of American Association for Pediatric Ophthalmology and Strabismus

      Volume: 22 Issue: 5 Pages: 401-403.e1

    • DOI

      10.1016/j.jaapos.2018.03.016

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Journal Article] Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome.2018

    • Author(s)
      Horinouchi T, Nozu K, Yamamura T, Minamikawa S, Omori T, Nakanishi K, Fujimura J, Ashida A, Kitamura M, Kawano M, Shimabukuro W, Kitabayashi C, Imafuku A, Tamagaki K, Kamei K, Okamoto K, Fujinaga S, Oka M, Igarashi T, Miyazono A, Sawanobori E, Fujimaru R, Nakanishi K, Shima Y et al
    • Journal Title

      J Am Soc Nephrol.

      Volume: 29 Issue: 8 Pages: 2244-2254

    • DOI

      10.1681/asn.2018030228

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-15K09694
  • [Journal Article] 【腎臓学 この一年の進歩】 遺伝性腎疾患2018

    • Author(s)
      野津 寛大, 飯島 一誠
    • Journal Title

      日本腎臓学会誌

      Volume: 61巻1号 Pages: 18-22

    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Journal Article] Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease2018

    • Author(s)
      Minamikawa S, Nozu K, Nozu Y, Yamamura T, Taniguchi-Ikeda M, Nakanishi K, Fujimura J, Horinouchi T, Shima Y, Nakanishi K, Hattori M, Kanda K, Tanaka R, Morisada N, Nagano C, Sakakibara N, Nagase H, Morioka I, Kaito H, Iijima K.
    • Journal Title

      Journal of Human Genetics

      Volume: 63 Issue: 5 Pages: 589-595

    • DOI

      10.1038/s10038-018-0415-1

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18K08243
  • [Journal Article] Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene2018

    • Author(s)
      Nakanishi Keita、Okamoto Takayuki、Nozu Kandai、Hara Shigeo、Sato Yasuyuki、Hayashi Asako、Takahashi Toshiyuki、Nagano China、Sakakibara Nana、Horinouchi Tomoko、Fujimura Junya、Minamikawa Shogo、Yamamura Tomohiko、Rossanti Rini、Nagase Hiroaki、Kaito Hiroshi、Ariga Tadashi、Iijima Kazumoto
    • Journal Title

      Clinical and Experimental Nephrology

      Volume: 23 Issue: 5 Pages: 669-675

    • DOI

      10.1007/s10157-018-1682-z

    • NAID

      120006644119

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-17K16262, KAKENHI-PROJECT-18K15712
  • [Journal Article] Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases2018

    • Author(s)
      Nagano C, Nozu K, Morisada N, Yazawa M, Ichikawa D, Numasawa K, Kourakata H, Matsumura C, Tazoe S, Tanaka R, Yamamura T, Minamikawa S, Horinouchi T, Nakanishi K, Fujimura J, Sakakibara N, Nozu Y, Ye MJ, Kaito H, Iijima K
    • Journal Title

      Clinical and Experimental Nephrology

      Volume: 印刷中 Issue: 4 Pages: 881-888

    • DOI

      10.1007/s10157-018-1534-x

    • NAID

      120006624236

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-16K19642, KAKENHI-PROJECT-18K08243
  • [Journal Article] The utility of urinary CD80 as a diagnostic marker in patients with renal diseases2018

    • Author(s)
      Minamikawa Shogo、Nozu Kandai、Maeta Shingo、Yamamura Tomohiko、Nakanishi Keita、Fujimura Junya、Horinouchi Tomoko、Nagano China、Sakakibara Nana、Nagase Hiroaki、Shima Hideaki、Noda Kenta、Ninchoji Takeshi、Kaito Hiroshi、Iijima Kazumoto
    • Journal Title

      Scientific Reports

      Volume: 8 Issue: 1 Pages: 17322-17322

    • DOI

      10.1038/s41598-018-35798-2

    • NAID

      120006543320

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Journal Article] Rituximab therapy for refractory steroid-resistant nephrotic syndrome in children2018

    • Author(s)
      Kamei Koichi、Ishikura Kenji、Sako Mayumi、Ito Shuichi、Nozu Kandai、Iijima Kazumoto
    • Journal Title

      Pediatric Nephrology

      Volume: 印刷中 Issue: 1 Pages: 17-24

    • DOI

      10.1007/s00467-018-4166-1

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Journal Article] ステロイド感受性ネフローゼ症候群とゲノムワイド関連解析2018

    • Author(s)
      飯島 一誠, 堀之内 智子, 野津 寛大
    • Journal Title

      【ネフローゼ症候群-MCNS/FSGSの最新知見】 病因、病態、病理学

      Volume: 85巻6号 Pages: 777-781

    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Journal Article] Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genes2018

    • Author(s)
      Yamamura Tomohiko、Nozu Kandai、Ueda Hiroaki、Fujimaru Rika、Hisatomi Ryutaro、Yoshida Yoko、Kato Hideki、Nangaku Masaomi、Miyata Toshiyuki、Sawai Toshihiro、Minamikawa Shogo、Kaito Hiroshi、Matsuo Masafumi、Iijima Kazumoto
    • Journal Title

      Journal of Human Genetics

      Volume: Epub ahead of print Issue: 6 Pages: 755-759

    • DOI

      10.1038/s10038-018-0436-9

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17K16073, KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-16K09834
  • [Journal Article] Cryptic exon activation in SLC12A3 in Gitelman syndrome.2017

    • Author(s)
      Nozu K, Nozu Y, Nakanishi K, Konomoto T, Horinouchi T, Shono A, Morisada N, Minamikawa S, Yamamura T, Fujimura J, Nakanishi K, Ninchoji T, Kaito H, Morioka I, Taniguchi-Ikeda M, Vorechovsky I, Iijima K
    • Journal Title

      J Hum Genet.

      Volume: 62 Issue: 2 Pages: 335-337

    • DOI

      10.1038/jhg.2016.129

    • NAID

      40021065185

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26461632, KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-16K10066
  • [Journal Article] A comparison of splicing assays to detect an intronic variant of the OCRL gene in Lowe syndrome2017

    • Author(s)
      Nakanishi Keita、Nozu Kandai、Hiramoto Ryugo、Minamikawa Shogo、Yamamura Tomohiko、Fujimura Junya、Horinouchi Tomoko、Ninchoji Takeshi、Kaito Hiroshi、Morisada Naoya、Ishimori Shingo、Nakanishi Koichi、Morioka Ichiro、Awano Hiroyuki、Matsuo Masafumi、Iijima Kazumoto
    • Journal Title

      European Journal of Medical Genetics

      Volume: 60 Issue: 12 Pages: 631-634

    • DOI

      10.1016/j.ejmg.2017.08.001

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Journal Article] Pseudo-Bartter syndrome in an infant with renal hypo/dysplasia: <i>PAX2</i> mutation identified by next-generation sequencing led to the diagnosis, renal coloboma syndrome2017

    • Author(s)
      波多江 健、慶田 裕美、檜山 麻衣子、黒木 理恵、黒川 麻里、森貞 直哉、野津 寛大、飯島 一誠
    • Journal Title

      Japanese journal of pediatric nephrology

      Volume: 30 Issue: 1 Pages: 54-59

    • DOI

      10.3165/jjpn.cr.2016.0105

    • NAID

      130006789708

    • ISSN
      0915-2245, 1881-3933
    • Language
      Japanese
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Journal Article] A case of mild phenotype Alport syndrome caused by COL4A3 mutations2017

    • Author(s)
      Kamijo Masafumi、Kitamura Mineaki、Muta Kumiko、Uramatsu Tadashi、Obata Yoko、Nozu Kandai、Kaito Hiroshi、Iijima Kazumoto、Mukae Hiroshi、Nishino Tomoya
    • Journal Title

      CEN Case Reports

      Volume: 6 Issue: 2 Pages: 189-193

    • DOI

      10.1007/s13730-017-0273-2

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189
  • [Journal Article] Natural history and genotype-phenotype correlation in female X-linked Alport syndrome.2017

    • Author(s)
      Yamamura T, Nozu K, Fu XJ, Nozu Y, Ye MJ, Shono A, Yamanouchi S, Minamikawa S, Morisada N, Nakanishi K, Shima Y, Yoshikawa N, Ninchoji T, Morioka I, Kaito H, Iijima K
    • Journal Title

      Kideny Int Rep.

      Volume: 印刷中

    • NAID

      120006373817

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Journal Article] Natural History and Genotype?Phenotype Correlation in Female X-Linked Alport Syndrome2017

    • Author(s)
      Yamamura Tomohiko、Nozu Kandai、Fu Xue Jun、Nozu Yoshimi、Ye Ming Juan、Shono Akemi、Yamanouchi Satoko、Minamikawa Shogo、Morisada Naoya、Nakanishi Koichi、Shima Yuko、Yoshikawa Norishige、Ninchoji Takeshi、Morioka Ichiro、Kaito Hiroshi、Iijima Kazumoto
    • Journal Title

      Kidney Int Rep.

      Volume: 2 Issue: 5 Pages: 850-855

    • DOI

      10.1016/j.ekir.2017.04.011

    • NAID

      120006373817

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-16K10066, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-15K09695, KAKENHI-PROJECT-16K19642
  • [Journal Article] Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin Deposits2017

    • Author(s)
      Tsuji Yurika、Nozu Kandai、Sofue Tadashi、Hara Shigeo、Nakanishi Keita、Yamamura Tomohiko、Minamikawa Shogo、Nozu Yoshimi、Kaito Hiroshi、Fujimura Junya、Horinouchi Tomoko、Morisada Naoya、Morioka Ichiro、Taniguchi-Ikeda Mariko、Matsuo Masafumi、Iijima Kazumoto
    • Journal Title

      Nephron

      Volume: 138 Issue: 2 Pages: 166-171

    • DOI

      10.1159/000484209

    • NAID

      120006867371

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Journal Article] Diversity of renal phenotypes in patients with WDR19 mutations: Two case reports2017

    • Author(s)
      Yoshikawa Takahisa、Kamei Koichi、Nagata Hiroko、Saida Ken、Sato Mai、Ogura Masao、Ito Shuichi、Miyazaki Osamu、Urushihara Maki、Kondo Shuji、Sugawara Noriko、Ishizuka Kiyonobu、Hamasaki Yuko、Shishido Seiichiro、Morisada Naoya、Iijima Kazumoto、Nagata Michio、Yoshioka Takako、Ogata Kentaro、Ishikura Kenji
    • Journal Title

      Nephrology

      Volume: 22 Issue: 7 Pages: 566-571

    • DOI

      10.1111/nep.12996

    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Journal Article] Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis.2017

    • Author(s)
      Nozu K, Minamikawa S, Yamada S, Oka M, Yanagita M, Morisada N, Fujinaga S, Nagano C, Gotoh Y, Takahashi E, Morishita T, Yamamura T, Ninchoji T, Kaito H, Morioka I, Nakanishi K, Vorechovsky I, Iijima K
    • Journal Title

      J Hum Genet.

      Volume: Epub 2017 Mar 9. Issue: 7 Pages: 733-735

    • DOI

      10.1038/jhg.2017.28

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26461632, KAKENHI-PROJECT-17H04189
  • [Journal Article] Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically2017

    • Author(s)
      Imafuku Aya、Nozu Kandai、Sawa Naoki、Hasegawa Eiko、Hiramatsu Rikako、Kawada Masahiro、Hoshino Junichi、Tanaka Kiho、Ishii Yasuo、Takaichi Kenmei、Fujii Takeshi、Ohashi Kenichi、Iijima Kazumoto、Ubara Yoshifumi
    • Journal Title

      Nephrology

      Volume: 印刷中 Issue: 10 Pages: 940-947

    • DOI

      10.1111/nep.13115

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189
  • [Journal Article] Diagnostic strategy for inherited hypomagnesemia.2017

    • Author(s)
      Horinouchi T, Nozu K, Kamiyoshi N, Kamei K, Togawa H, Shima Y, Urahama Y, Yamamura T, Minamikawa S, Nakanishi K, Fujimura J, Morioka I, Ninchoji T, Kaito H, Nakanishi K, Iijima K.
    • Journal Title

      Clin Exp Nephrol.

      Volume: 印刷中 Issue: 6 Pages: 1003-1010

    • DOI

      10.1007/s10157-017-1396-7

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-15K09691
  • [Journal Article] An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis2017

    • Author(s)
      Yamamura Tomohiko、Nozu Kandai、Miyoshi Yuya、Nakanishi Keita、Fujimura Junya、Horinouchi Tomoko、Minamikawa Shogo、Mori Nobuo、Fujimaru Rika、Nakanishi Koichi、Ninchoji Takeshi、Kaito Hiroshi、Mariko Taniguchi-Ikeda、Morioka Ichiro、Matsuo Masafumi、Iijima Kazumoto
    • Journal Title

      BMC Nephrology

      Volume: 18 Issue: 1 Pages: 353-353

    • DOI

      10.1186/s12882-017-0774-4

    • NAID

      120006377621

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Journal Article] 次世代シークエンサーを用いた先天性腎尿路奇形(CAKUT)の原因遺伝子解析2016

    • Author(s)
      森貞 直哉, 庄野 朱美, 野津 寛大, 叶 明娟, 神田 祥一郎, 井藤 奈央子, 亀井 宏一, 伊藤 秀一, 山本 勝輔, 里村 憲一, 田中 亮二郎, 西尾 久英, 飯島 一誠
    • Journal Title

      発達腎研究会誌

      Volume: 24 Pages: 13-15

    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Journal Article] A Novel Mutation in a Japanese Family with X-linked Alport Syndrome.2016

    • Author(s)
      Abe Y, Iyoda M, Nozu K, Hibino S, Hihara K, Yamaguchi Y, Yamamura T, Minamikawa S, Iijima K, Shibata T, Itabashi K
    • Journal Title

      Intern Med.

      Volume: 55 Pages: 2843-2847

    • NAID

      130005605859

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Journal Article] New-onset diabetes after renal transplantation in a patient with a novel HNF1B mutation2016

    • Author(s)
      Kanda S, Morisada N, Kaneko N, Yabuuchi T, Nawashiro Y, Tada N, Nishiyama K, Miyai T, Sugawara N, Ishizuka K, Chikamoto H, Akioka Y, Iijima K, Hattori M.
    • Journal Title

      Pediatric Transplantation

      Volume: 20 Issue: 3 Pages: 467-471

    • DOI

      10.1111/petr.12690

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-15K21385, KAKENHI-PROJECT-26293203
  • [Journal Article] Alternative splicing of a cryptic exon embedded in intron 6 of SMN1 and SMN2.2016

    • Author(s)
      Yoshimoto S, Harahap NI, Hamamura Y, Ar Rochmah M, Shima A, Morisada N, Shinohara M, Saito T, Saito K, Lai PS, Matsuo M, Awano H, Morioka I, Iijima K, Nishio H.
    • Journal Title

      Hum Genome Var.

      Volume: 3 Issue: 1 Pages: 16040-16040

    • DOI

      10.1038/hgv.2016.40

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Journal Article] Early RAAS Blockade Exerts Renoprotective Effects in Autosomal Recessive Alport Syndrome.2016

    • Author(s)
      Uchida N, Kumagai N, Nozu K, Fu XJ, Iijima K, Kondo Y, Kure S
    • Journal Title

      Tohoku J Exp Med.

      Volume: 240 Pages: 251-257

    • NAID

      130005170640

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Journal Article] Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1.2016

    • Author(s)
      Kamiyoshi N, Nozu K, Urahama Y, Matsunoshita N, Yamamura T, Minamikawa S, Ninchoji T, Morisada N, Nakanishi K, Kaito H, Iijima K.
    • Journal Title

      Clin Exp Nephrol.

      Volume: 20 Issue: 2 Pages: 253-257

    • DOI

      10.1007/s10157-015-1160-9

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-26461618, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26860800, KAKENHI-PROJECT-15K09261
  • [Journal Article] Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits.2016

    • Author(s)
      Ohtsubo H, Okada T, Nozu K, Takaoka Y, Shono A, Asanuma K, Zhang L, Nakanishi K, Taniguchi-Ikeda M, Kaito H, Iijima K, Nakamura SI
    • Journal Title

      Pediatr Nephrol.

      Volume: 58 Issue: 9 Pages: 1459-1467

    • DOI

      10.1007/s00467-016-3368-7

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-16K10066
  • [Journal Article] Rare renal ciliopathies in non-consanguineous families that were identified by targeted resequencing.2016

    • Author(s)
      Yamamura T, Morisada N, Nozu K, Minamikawa S, Ishimori S, Toyoshima D, Ninchoji T, Yasui M, Taniguchi-Ikeda M, Morioka I, Nakanishi K, Nishio H, Iijima K.
    • Journal Title

      Clin Exp Nephrol.

      Volume: 20 Issue: 1 Pages: 136-142

    • DOI

      10.1007/s10157-016-1256-x

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26461632, KAKENHI-PROJECT-15K09261
  • [Journal Article] 腎・泌尿器 Bartter症候群2016

    • Author(s)
      野津寛大
    • Journal Title

      小児科診療

      Volume: 79 Pages: 294-294

    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Journal Article] 腎・泌尿器 Gitelman症候群2016

    • Author(s)
      野津寛大
    • Journal Title

      小児科診療

      Volume: 79 Pages: 300-300

    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Journal Article] Diverse Renal Phenotypes Observed in a Single Family with a Genetic Mutation in Paired Box Protein 2.2016

    • Author(s)
      Iwafuchi Y, Morioka T, Morita T, Yanagihara T, Oyama Y, Morisada N, Iijima K, Narita I.
    • Journal Title

      Case Rep Nephrol Dial.

      Volume: 58 Issue: 1 Pages: 83-89

    • DOI

      10.1159/000445679

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Journal Article] Female X-linked Alport syndrome with somatic mosaicism2016

    • Author(s)
      Yokota K, Nozu K, Minamikawa S, Yamamura T, Nakanishi K, Kaneda H, Hamada R, Nozu Y, Shono A, Ninchoji T, Morisada N, Ishimori S, Fujimura J, Horinouchi T, Kaito H, Nakanishi K, Morioka I, Taniguchi-Ikeda M, Iijima K.
    • Journal Title

      Clin Exp Nephrol.

      Volume: 印刷中 Issue: 5 Pages: 877-883

    • DOI

      10.1007/s10157-016-1352-y

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-16K10066, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-16K19642
  • [Journal Article] Somatic mosaicism and variant frequency detected by next-generation sequencing in X-linked Alport syndrome.2016

    • Author(s)
      Fu XJ, Nozu K, Kaito H, Ninchoji T, Morisada N, Nakanishi K, Yoshikawa N, Ohtsubo H, Matsunoshita N, Kamiyoshi N, Matsumura C, Takagi N, Maekawa K, Taniguchi-Ikeda M, Iijima K
    • Journal Title

      Eur J Hum Genet

      Volume: 24 Issue: 3 Pages: 387-391

    • DOI

      10.1038/ejhg.2015.113

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26461618, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26860800, KAKENHI-PROJECT-15K09695
  • [Journal Article] Next-generation sequencing discloses a nonsense mutation in the dystrophin gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother.2016

    • Author(s)
      Taniguchi-Ikeda M, Takeshima Y, Lee T, Nishiyama M, Awano H, Yagi M, Unzaki A, Nozu K, Nishio H, Matsuo M, Kurahashi H, Toda T, Morioka I, Iijima K.
    • Journal Title

      J Hum Genet.

      Volume: 61 Issue: 4 Pages: 351-355

    • DOI

      10.1038/jhg.2015.157

    • NAID

      40020802923

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-26461632
  • [Journal Article] Risk factors for relapse and long-term outcome in steroid-dependent nephrotic syndrome treated with rituximab.2016

    • Author(s)
      Kamei K, Ogura M, Sato M, Sako M, Iijima K, Ito S.
    • Journal Title

      Pediatr Nephrol.

      Volume: 31 Issue: 1 Pages: 89-95

    • DOI

      10.1007/s00467-015-3197-0

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Journal Article] Insignificant impact of VUR on the progression of CKD in children with CAKUT.2016

    • Author(s)
      Ishikura K, Uemura O, Hamasaki Y, Nakai H, Ito S, Harada R, Hattori M, Ohashi Y, Tanaka R, Nakanishi K, Kaneko T, Iijima K, Honda M; Pediatric CKD Study Group in Japan in conjunction with the Committee of Measures for Pediatric CKD of the Japanese Society for Pediatric Nephrology
    • Journal Title

      Pediatr Nephrol

      Volume: 31 Issue: 1 Pages: 105-112

    • DOI

      10.1007/s00467-015-3196-1

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26461618, KAKENHI-PROJECT-25461637, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15H04880
  • [Journal Article] Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics2016

    • Author(s)
      Matsunoshita N, Nozu K, Shono A, Nozu Y, Fu XJ, Morisada N, Kamiyoshi N, Ohtsubo H, Ninchoji T, Minamikawa S, Yamamura T, Nakanishi K, Yoshikawa N, Shima Y, Kaito H, Iijima K
    • Journal Title

      Genetics in Medicine

      Volume: 18 Issue: 2 Pages: 180-188

    • DOI

      10.1038/gim.2015.56

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-26461618, KAKENHI-PROJECT-26860800, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15K09695
  • [Journal Article] Genetic, clinical and pathological backgrounds in autosomal dominant Alport syndrome.2016

    • Author(s)
      Kamiyoshi N, Nozu K, Fu XJ, Morisada N, Nozu Y, Imafuku A, Miura K, Yamamura T, Minamikawa S, Shono A, Ninchoji T, Kaito H, Morioka I, Nakanishi K, Yoshikawa N, Iijima K.
    • Journal Title

      Clin J Am Soc Nephrol.

      Volume: 11

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Journal Article] A 12p13 GRIN2B deletion is associated with developmental delay and macrocephaly.2016

    • Author(s)
      Morisada N, Ioroi T, Taniguchi-Ikeda M, Juan Ye M, Okamoto N, Yamamoto T, Iijima K.
    • Journal Title

      Hum Genome Var.

      Volume: 3 Issue: 1 Pages: 16029-16029

    • DOI

      10.1038/hgv.2016.29

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Journal Article] Daughter and mother with orofaciodigital syndrome type 1 and glomerulocystic kidney disease.2016

    • Author(s)
      Iijima T, Hoshino J, Mise K, Sumida K, Suwabe T, Hayami N, Ueno T, Takaichi K, Fujii T, Ohashi K, Morisada N, Iijima K, Ubara Y.
    • Journal Title

      Hum Pathol.

      Volume: 55 Pages: 24-29

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Journal Article] Female X-linked Alport syndrome with somatic mosaicism.2016

    • Author(s)
      Yokota K, Nozu K, Minamikawa S, Yamamura T, Nakanishi K, Kaneda H, Hamada R, Nozu Y, Shono A, Ninchoji T, Morisada N, Ishimori S, Fujimura J, Horinouchi T, Kaito H, Nakanishi K, Morioka I, Taniguchi-Ikeda M, Iijima K
    • Journal Title

      Clin Exp Nephrol.

      Volume: Epub 2016 Oct 31.

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Journal Article] Telomeric Region of the Spinal Muscular Atrophy Locus Is Susceptible to Structural Variations.2016

    • Author(s)
      Noguchi Y, Onishi A, Nakamachi Y, Hayashi N, Harahap NI, Rochmah MA, Shima A, Yanagisawa S, Morisada N, Nakagawa T, Iijima K, Kasagi S, Saegusa J, Kawano S, Shinohara M, Tairaku S, Saito T, Kubo Y, Saito K, Nishio H.
    • Journal Title

      Pediatr Neurol

      Volume: 58 Pages: 83-89

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Journal Article] Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome.2016

    • Author(s)
      Kamiyoshi N, Nozu K, Fu XJ, Morisada N, Nozu Y, Ye MJ, Imafuku A, Miura K, Yamamura T, Minamikawa S, Shono A, Ninchoji T, Morioka I, Nakanishi K, Yoshikawa N, Kaito H, Iijima K
    • Journal Title

      Clin J Am Soc Nephrol.

      Volume: 11 Issue: 8 Pages: 1441-1449

    • DOI

      10.2215/cjn.01000116

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-15K09682, KAKENHI-PROJECT-15K09695, KAKENHI-PROJECT-16K10066
  • [Journal Article] Acute kidney injury in type 3 Bartter syndrome: Angiotensin-converting enzyme inhibitors as a cause.2016

    • Author(s)
      Nagao R, Suzuki S, Kawashima H, Nozu K, Iijima K
    • Journal Title

      Pediatr Int

      Volume: 58 Issue: 12 Pages: 1373-1374

    • DOI

      10.1111/ped.13100

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Journal Article] Combined Alport syndrome and Klinefelter syndrome.2016

    • Author(s)
      Nishida M, Hashimoto F, Kaito H, Nozu K, Iijima K, Asada D, Hamaoka K.
    • Journal Title

      Pediatr Int.

      Volume: 58 Issue: 2 Pages: 152-155

    • DOI

      10.1111/ped.12743

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Journal Article] Biallelic mutations in nuclear pore complex subunit NUP107 cause early-childhood-onset steroid-resistant nephrotic syndrome2015

    • Author(s)
      Miyake N, Tsukaguchi H, Koshimizu E, Shono A, Matsunaga S, Shiina M, Mimura Y, Imamura S, Hirose T, Okudela K, Nozu K, Akioka Y, Hattori M, Yoshikawa N, Kitamura A, Cheong HI, Kagami S, Yamashita M, Fujita A, Miyatake S, Tsurusaki Y, Nakashima M, Saitsu H, Ohashi K, Imamoto N, Ryo A, Ogata K, Iijima K, Matsumoto N
    • Journal Title

      Am J Hum Genet

      Volume: 97(4) Issue: 4 Pages: 555-566

    • DOI

      10.1016/j.ajhg.2015.08.013

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26330331, KAKENHI-PROJECT-26461246, KAKENHI-PROJECT-26461549, KAKENHI-PROJECT-15K19660, KAKENHI-ORGANIZER-24118001, KAKENHI-PLANNED-24118005, KAKENHI-PLANNED-24118007, KAKENHI-PROJECT-25293235, KAKENHI-PROJECT-26293203
  • [Journal Article] Rituximab Treatment for Nephrotic Syndrome in Children.2015

    • Author(s)
      Iijima K, Sako M, Nozu K.
    • Journal Title

      Curr Pediatr Rep.

      Volume: 3 Issue: 1 Pages: 71-77

    • DOI

      10.1007/s40124-014-0065-5

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Journal Article] Alport症候群の軽症亜型2015

    • Author(s)
      野津寛大、飯島一誠
    • Journal Title

      Annual Review2015腎臓

      Volume: 2015 Pages: 75-79

    • Data Source
      KAKENHI-PROJECT-25893131
  • [Journal Article] Long-term outcome of childhood IgA nephropathy with minimal proteinuria.2015

    • Author(s)
      Higa A, Shima Y, Hama T, Sato M, Mukaiyama H, Togawa H, Tanaka R, Nozu K, Sako M, Iijima K, Nakanishi K, Yoshikawa N.
    • Journal Title

      Pediatr Nephrol.

      Volume: 30(12) Issue: 12 Pages: 2121-7

    • DOI

      10.1007/s00467-015-3176-5

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-15K09695, KAKENHI-PROJECT-26461618, KAKENHI-PROJECT-26293203
  • [Journal Article] A Novel <i>UMOD</i> Gene Mutation Associated with Uromodulin-associated Kidney Disease in a Young Woman with Moderate Kidney Dysfunction2015

    • Author(s)
      Kuma A, Tamura M, Ishimatsu N, Miyamoto T, Serino R, Ishimori S, Morisada N, IijimaK, Takeuchi M, Abe H, Otsuji Y:
    • Journal Title

      Intern. Med.

      Volume: 54 Issue: 6 Pages: 631-635

    • DOI

      10.2169/internalmedicine.54.3151

    • NAID

      130004903078

    • ISSN
      0918-2918, 1349-7235
    • Language
      English
    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-25461081, KAKENHI-PROJECT-15K09261
  • [Journal Article] X-linked Alport syndrome associated with a synonymous p.Gly292Gly mutation alters the splicing donor site of the type IV collagen alpha chain 5 gene.2015

    • Author(s)
      Fu XJ, Nozu K, Eguchi A, Nozu Y, Morisada N, Shono A, Taniguchi-Ikeda M, Shima Y, Nakanishi K, Vorechovsky I, Iijima K
    • Journal Title

      Clin Exp Nephrol.

      Volume: 20 Issue: 5 Pages: 699-702

    • DOI

      10.1007/s10157-015-1197-9

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15K09261
  • [Journal Article] Bartter症候群、Gitelman症候群2015

    • Author(s)
      松野下夏樹 野津寛大 飯島一誠
    • Journal Title

      日本腎臓学会誌

      Volume: 57 Pages: 743-750

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Journal Article] Bartter症候群・Gitelman症候群:遺伝性塩類喪失性尿細管機能異常症2015

    • Author(s)
      野津寛大
    • Journal Title

      内科

      Volume: 6 Pages: 1039-1039

    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Journal Article] ヒトCAKUTの原因遺伝子解析2015

    • Author(s)
      森貞 直哉, 野津 寛大, 亀井 宏一, 伊藤 秀一, 田中 亮二郎, 飯島 一誠
    • Journal Title

      発達腎研究会誌

      Volume: 23 Pages: 19-22

    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Journal Article] Natural history of genetically proven autosomal recessive Alport syndrome2014

    • Author(s)
      Oka M, Nozu K, Kaito H, Fu XJ, Nakanishi K, Hashimura Y, Morisada N, Yan K, Matsuo M, Yoshikawa N, Vorechovsky I, Iijima K
    • Journal Title

      Pediatr Nephrol

      Volume: 29 Issue: 9 Pages: 1535-1544

    • DOI

      10.1007/s00467-014-2797-4

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24390265, KAKENHI-PROJECT-25893131, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26461618
  • [Journal Article] X-Linked Alport Syndrome Caused by Splicing Mutations in COL4A52014

    • Author(s)
      Nozu, K. Vorechovsky, I. Kaito, H. Fu, X. J. Nakanishi, K. Hashimura, Y. Hashimoto, F. Kamei, K. Ito, S. Kaku, Y. Imasawa, T. Ushijima, K. Shimizu, J. Makita, Y. Konomoto, T. Yoshikawa, N. Iijima, K.
    • Journal Title

      Clinical journal of the American Society of Nephrology : CJASN

      Volume: 9 Issue: 11 Pages: 1958-64

    • DOI

      10.2215/cjn.04140414

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-25893131, KAKENHI-PROJECT-26293203
  • [Journal Article] 【腎臓病のすべて】腎臓病各論 診断とエビデンスに基づいた治療 遺伝性腎炎と先天性ネフローゼ症候群2014

    • Author(s)
      貝藤裕史、飯島一誠
    • Journal Title

      医学のあゆみ

      Volume: 249 Pages: 845-850

    • Data Source
      KAKENHI-PROJECT-26293203
  • [Journal Article] 【内科疾患最新の治療-明日への指針】Alport症候群2014

    • Author(s)
      野津寛大、飯島一誠
    • Journal Title

      内科

      Volume: 6 Pages: 1172-1173

    • Data Source
      KAKENHI-PROJECT-26293203
  • [Journal Article] Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain2014

    • Author(s)
      Hashimura Y, Nozu K, Kaito H, Nakanishi K, Fu XJ, Ohtsubo H, Hashimoto F, Oka M, Ninchoji T, Ishimori S, Morisada N, Matsunoshita N, Kamiyoshi N, Yoshikawa N, Iijima K
    • Journal Title

      Kidney Int

      Volume: 85 Issue: 5 Pages: 1208-1213

    • DOI

      10.1038/ki.2013.479

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24390265, KAKENHI-PROJECT-25893131, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26461618
  • [Journal Article] Diffuse glomerular nodular lesions in diabetic pigs carrying a dominant-negative mutant hepatocyte nuclear factor 1-alpha, an inheritant diabetic gene in humans2014

    • Author(s)
      Hara S, Umeyama K, Yokoo T, Nagashima H, Nagata M
    • Journal Title

      PLoS One

      Volume: 9(3)

    • NAID

      120007130512

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] The problem of transition from pediatric to adult healthcare in patients with steroid-sensitive nephrotic syndrome (SSNS): a survey of the experts2014

    • Author(s)
      Honda M, Iijima K, Ishikura K, Kaneko K
    • Journal Title

      Clin Exp Nephrol

      Volume: (Epub ahead of print)

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Rituximab treatment combined with methylprednisolone pulse therapy and immunosuppressants for childhood steroid-resistant nephrotic syndrome2014

    • Author(s)
      Kamei K, Okada M, Sato M, Fujimaru T, Ogura M, Nakayama M, Kaito H, Iijima K, Ito S
    • Journal Title

      Pediatr Nephrol

      Volume: 29(7) Pages: 1181-7

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Natural history of genetically proven autosomal recessive Alport syndrome2014

    • Author(s)
      Oka M, Nozu K, Kaito H, Fu XJ, Nakanishi K, Hashimura Y, Morisada N, Yan K, Matsuo M, Yoshikawa N, Vorechovsky I, Iijima K
    • Journal Title

      Pediatr Nephrol

      Volume: (Epub ahead of print)

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Acute kidney injury after acute gastroenteritis in an infant with hereditary hypouricemia2014

    • Author(s)
      Kamei K, Ogura M, Ishimori S, Kaito H, Iijima K, Ito S
    • Journal Title

      Eur JPediatr

      Volume: 173(2) Pages: 247-913

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Alport syndrome caused by a COL4A5 deletion and exonization of an adjacent AluY.2014

    • Author(s)
      Nozu K, Iijima K, Ohtsuka Y, Fu XJ, Kaito H, Nakanishi K, Vorechovsky I
    • Journal Title

      Mol Genet Genomic Med

      Volume: 2 Issue: 5 Pages: 451-451

    • DOI

      10.1002/mgg3.89

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-25461648, KAKENHI-PROJECT-25893131, KAKENHI-PROJECT-26293203
  • [Journal Article] Alport症候群2014

    • Author(s)
      野津寛大、飯島一誠
    • Journal Title

      内科

      Volume: 6 Pages: 1172-73

    • NAID

      10025170337

    • Data Source
      KAKENHI-PROJECT-25893131
  • [Journal Article] Cyclosporine C2 Monitoring for the Treatment of Frequently Relapsing Nephrotic Syndrome in Children: A Multicenter Randomized Phase II Trial.2014

    • Author(s)
      Iijima K, Sako M, Oba MS, Ito S, Hataya H, Tanaka R, Ohwada Y, Kamei K, Ishikura K, Yata N, Nozu K, Honda M, Nakamura H, Nagata M, Ohashi Y, Nakanishi K, Yoshikawa N. : Japanese Study Group of Kidney Disease in Children.
    • Journal Title

      Clin J Am Soc Nephrol

      Volume: 9(2) Issue: 2 Pages: 271-8

    • DOI

      10.2215/cjn.13071212

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591192, KAKENHI-PROJECT-24390265, KAKENHI-PROJECT-25461637, KAKENHI-PROJECT-26461618
  • [Journal Article] Cyclosporine C2 monitoring for the treatment of frequently relapsing nephrotic syndrome in children : a multicenter randomized phase II trial2014

    • Author(s)
      Iijima K, Sako M, Oba MS, Ito S, Hataya H, Tanaka R, Ohwada Y, Kamei K, Ishikura K, Yata N, Nozu K, Honda M, Nakamura H, Nagata M, Ohashi Y, Nakanishi K, Yoshikawa N; Japanese Study Group of Kidney Disease in Children
    • Journal Title

      Clin J Am Soc Nephrol

      Volume: 9(2) Pages: 271-8

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IVα5 chain2014

    • Author(s)
      Hashimura Y, Nozu K, Kaito H, Nakanishi K, Fu XJ, Ohtsubo H, Hashimoto F, Oka M, Ninchoji T, Ishimori S, Morisada N, Matsunoshita N, Kamiyoshi N, Yoshikawa N, Iijima K
    • Journal Title

      Kidney Int.

      Volume: 85(5) Pages: 1208-13

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Molecular background of urate transporter genes in patients with exercise-induced acute kidney injury2013

    • Author(s)
      Kaito H, Ishimori S, Nozu K, Shima Y, Nakanishi K, Yoshikawa N, Iijima K
    • Journal Title

      Am J Nephrol

      Volume: 38(4) Pages: 316-20

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Two-year outcome of the ISKDC regimen and frequent-relapsing risk in children with idiopathic nephrotic syndrome2013

    • Author(s)
      Nakanishi K, Iijima K, Ishikura K, Hataya H, Nakazato H, Sasaki S, Honda M, Yoshikawa N; Japanese Study Group of Renal Disease in Children
    • Journal Title

      Clin J Am Soc Nephrol

      Volume: 8(5) Pages: 756-62

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Spontaneous remission in children with IgA nephropathy2013

    • Author(s)
      Shima Y, Nakanishi K, Hama T, Mukaiyama H, Togawa H, Sako M, Kaito H, Nozu K, Tanaka R, Iijima K, Yoshikawa N
    • Journal Title

      Pediatr Nephrol

      Volume: 28(1) Pages: 71-6

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] The direction and role of phenotypic transition between podocytes and parietal epithelial cells in focal segmental glomerulosclerosis2013

    • Author(s)
      Sakamoto K, Ueno T, Kobayashi N, Hara S, Takashima Y, Pastan I, Matsusaka T, Nagata M
    • Journal Title

      Am J Physiol Renal Physiol

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Two-year outcome of the ISKDC regimen and frequent-relapsing risk in children with idiopathic nephrotic syndrome2013

    • Author(s)
      Koichi Nakanishi、Kazumoto Iijima、Kenji Ishikura、Satoshi Sasak、Masataka Honda、Norio Yosikawa
    • Journal Title

      Clin J Am Soc Nephrol

      Volume: Vol.8 Issue: 5 Pages: 756-762

    • DOI

      10.2215/cjn.09010912

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591176, KAKENHI-PROJECT-23591192, KAKENHI-PROJECT-24390265
  • [Journal Article] SLC26A3 gene analysis in patients with Bartter and Gitelman syndromes and the clinical characteristics of patients with unidentified mutations2013

    • Author(s)
      Ishimori S, Kaito H, Matsunoshita N, Otsubo H, Hashimoto F, Ninchoji T, Nozu K, Morisada N, Iijima K
    • Journal Title

      Kobe J Med Sci.

      Volume: 59(2)

    • NAID

      110009595389

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Establishment of a normal reference value for serumβ2 microglobulin in Japanese children : reevaluation of its clinical usefulness2013

    • Author(s)
      Ikezumi Y, Honda M, Matsuyama T, Ishikura K, Hataya H, Yata N, Nagai T, Fujita N, Ito S, Iijima K, Kaneko T, Uemura O
    • Journal Title

      Clin Exp Nephrol

      Volume: 17(1) Pages: 99-105

    • NAID

      10031169450

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Survey of rituximab treatment for childhood-onset refractory nephrotic syndrome2013

    • Author(s)
      Ito S, Kamei K, Ogura M, Udagawa T, Fujinaga S, Saito M, Sako M, Iijima K
    • Journal Title

      Pediatr Nephrol

      Volume: 28(2) Pages: 257-64

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Different phenotypes of HNF1ß deletion mutants in familial multicystic dysplastic kidneys2013

    • Author(s)
      Hasui M, Kaneko K, Tsuji S, Isozaki Y, Kimata T, Nozu Y, Nozu K, Iijima K
    • Journal Title

      Clin Nephrol

      Volume: 79(6)(PubMed PMID : 23725647) Pages: 484-7

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Molecular background of urate transporter geneMolecular background of urate transporter genes in patients with exercise-induced acute kidney injury.2013

    • Author(s)
      Kaito H, Ishimori Kaito H, Ishimori S, Nozu K, Shima Y, Nakanishi K, Yoshikawa N, Iijima K.
    • Journal Title

      Am J Nephrol.

      Volume: 38(4) Issue: 4 Pages: 629-629

    • DOI

      10.1159/000355430

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591192, KAKENHI-PROJECT-24390265, KAKENHI-PROJECT-24791082
  • [Journal Article] Henoch-Schönlein purpura nephritis in a patient with IgG4-related disease : a possible association2013

    • Author(s)
      Ito K, Yamada K, Mizushima I, Aizu M, Fujii H, Mizutomi K, Matsumura M, Hayashi K, Yamagishi M, Umehara H, Yamaguchi Y, Nagata M, Kawano M
    • Journal Title

      Clin Nephrol

      Volume: 79(3) Pages: 246-52

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Reference ranges for serum cystatin C measurements in Japanese children by using 4 automated assays2013

    • Author(s)
      Yata N, Uemura O, Honda M, Matsuyama T, Ishikura K, Hataya H, Nagai T, Ikezumi Y, Fujita N, Ito S, Iijima K, Saito M, Keneko T, Kitagawa T
    • Journal Title

      Clin Exp Nephrol

      Volume: 17(6) Pages: 872-6

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Endoplasmic reticulum stress with low-dose cyclosporine in frequently relapsing nephrotic syndrome2013

    • Author(s)
      Hama T, Nakanishi K, Mukaiyama H, Shima Y, Togawa H, Sako M, Nozu K, Iijima K, Yoshikawa N
    • Journal Title

      Pediatr Nephrol

      Volume: 28(6) Pages: 903-9

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] First Japanese case of Pierson syndrome with mutations in LAMB22013

    • Author(s)
      Togawa H, Nakanishi K, Mukaiyama H, Hama T, Shima Y, Nakano M, Fujita N, Iijima K, Yoshikawa N
    • Journal Title

      Pediatr Int.

      Volume: 55(2) Pages: 229-31

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Survey of rituximab treatment for childhood-onset refractory nephrotic syndrome.2013

    • Author(s)
      Ito S, Kemei K, Ogura M, Udagawa T, Fujinaga S, Saito M, Sako M, Iijima K
    • Journal Title

      Pediatr Nephrol

      Volume: 28 Issue: 2 Pages: 257-64

    • DOI

      10.1007/s00467-012-2319-1

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591196, KAKENHI-PROJECT-23591192
  • [Journal Article] Prospective 5-year follow-up of cyclosporine treatment in children with steroid-resistant nephrosis2013

    • Author(s)
      Hamasaki Y, Yoshikawa N, Nakazato H, Sasaki S, Iijima K, Nakanishi K, Matsuyama T, Ishikura K, Ito S, Kaneko T, Honda M; for Japanese Study Group of Renal Disease in Children
    • Journal Title

      Pediatr Nephrol

      Volume: 28(5) Pages: 765-71

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Two-year follow-up of a prospective clinical trial of cyclosporine for frequently relapsing nephrotic syndrome in children2012

    • Author(s)
      Ishikura K, Yoshikawa N, Nakazato H, Sasaki S, Iijima K, Nakanishi K, Matsuyama T, Ito S, Yata N, Ando T, Honda M; Japanese Study Group of Renal Disease in Children
    • Journal Title

      Clin J Am Soc Nephrol

      Volume: 7(10) Pages: 1576-83

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Is the new Schwartz equation derived from serum creatinine and body length suitable for evaluation of renal function in Japanese children?2012

    • Author(s)
      Uemura O, Honda M, Matsuyama T, Ishikura K, Hataya H, Nagai T, Ikezumi Y, Fujita N, Ito S, Iijima K; Japanese Society for Pediatric Nephrology, the Committee of Measures for Pediatric CKD
    • Journal Title

      Eur J Pediatr

      Volume: 171(9) Pages: 1401-4

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Focal segmental glomerulosclerosis in patients with complete deletion of one WT1 allele2012

    • Author(s)
      Iijima K, Someya T, Ito S, Nozu K, Nakanishi K, Matsuoka K, Ohashi H, Nagata M, Kamei K, Sasaki S
    • Journal Title

      Pediatrics

      Volume: 129(6)

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Renal biopsy criterion in children with asymptomatic constant isolated proteinuria2012

    • Author(s)
      Hama T, Nakanishi K, Shima Y, Mukaiyama H, Togawa H, Tanaka R, Hamahira K, Kaito H, Iijima K, Yoshikawa N
    • Journal Title

      Nephrol Dial Transplant

      Volume: 27(8) Pages: 3186-90

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Clinical and histological changes associated with corticosteroid therapy in IgG4-related tubulointerstitial nephritis2012

    • Author(s)
      Mizushima I, Yamada K, Fujii H, Inoue D, Umehara H, Yamagishi M, Yamaguchi Y, Nagata M, Matsumura M, Kawano M
    • Journal Title

      Mod Rheumatol

    • NAID

      10031127240

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Validity of the Oxford classification of IgA nephropathy in children2012

    • Author(s)
      Shima Y, Nakanishi K, Hama T, Mukaiyama H, Togawa H, Hashimura Y, Kaito H, Sako M, Iijima K, Yoshikawa N
    • Journal Title

      Pediatr Nephrol

      Volume: 27(5) Pages: 783-92

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Renal biopsy criterion in children with asymptomatic constant isolated proteinuria.2012

    • Author(s)
      Hama T, Nakanishi K, Shima Y, Mukaiyama H, Togawa H, Tanaka R, Hamahira K, Kaito H, Iijima K, Yoshikawa N
    • Journal Title

      Nephrol Dial Transplant.

      Volume: 27(8) Issue: 8 Pages: 3186-90

    • DOI

      10.1093/ndt/gfr750

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591192, KAKENHI-PROJECT-24390265, KAKENHI-PROJECT-24791082
  • [Journal Article] Metabolomics analysis of umbilical cord blood clarifies changes in saccharides associated with delivery method.2012

    • Author(s)
      Hashimoto F, Nishiumi S, Miyake O, Takeichi H, Chitose M, Ohtsubo H, Ishimori S, Ninchoji T, Hashimura Y, Kaito H, Morisada N, Morioka I, Fukuoka H, Yoshida M, Iijima K.
    • Journal Title

      Early Hum Dev

      Volume: 89(5) Issue: 5 Pages: 315-20

    • DOI

      10.1016/j.earlhumdev.2012.10.010

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Japanese Society for Pediatric Nephrology, the Committee of Measures for Pediatric CKD. Is the new Schwartz equation derived from serum creatinine and body length suitable for evaluation of renal function in Japanese children?2012

    • Author(s)
      Uemura O, Honda M, Matsuyama T, Ishikura K, Hataya H, Nagai T, Ikezumi Y, Fujita N, Ito S, Iijima K.
    • Journal Title

      Eur J Pediatr.

      Volume: 171(9) Pages: 1401-4

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Validity of the Oxford classification of IgA nephropathy in children.2012

    • Author(s)
      Shima Y, Nakanishi K, Hama T, Mukaiyama H, Togawa H, Hashimura Y, Kaito H, Sako M, Iijima K, Yoshikawa N
    • Journal Title

      Pediatr Nephrol.

      Volume: 27(5) Issue: 5 Pages: 783-92

    • DOI

      10.1007/s00467-011-2061-0

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591192, KAKENHI-PROJECT-24390265, KAKENHI-PROJECT-24791082
  • [Journal Article] Alport-like glomerular basement membrane changes with renal-coloboma syndrome.2012

    • Author(s)
      Ohtsubo H, Morisada N, Kaito H, Nagatani K, Nakanishi K, Iijima K.
    • Journal Title

      Pediatr Nephrol.

      Volume: 27(7) Issue: 7 Pages: 1189-92

    • DOI

      10.1007/s00467-012-2125-9

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Focal segmental glomerulosclerosis in patients with complete deletion of one WT1 allele.2012

    • Author(s)
      Iijima K, Someya T, Ito S, Nozu K, Nakanishi K, Matsuoka K, Ohashi H, Nagata M, Kamei K, Sasaki S
    • Journal Title

      Pediatrics

      Volume: 129 Issue: 6 Pages: e1621-e1625

    • DOI

      10.1542/peds.2011-1323

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591196, KAKENHI-PROJECT-23591192
  • [Journal Article] for the Japanese Study Group of Renal Disease in Children. Two-Year Follow-Up of a Prospective Clinical Trial of Cyclosporine for Frequently Relapsing Nephrotic Syndrome in Children.2012

    • Author(s)
      Ishikura K, Yoshikawa N, Nakazato H, Sasaki S, Iijima K, Nakanishi K, Matsuyama T, Ito S, Yata N, Ando T, Honda M
    • Journal Title

      Clin J Am Soc Nephrol

      Volume: 7 Issue: 10 Pages: 1576-1583

    • DOI

      10.2215/cjn.00110112

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591196, KAKENHI-PROJECT-23591176, KAKENHI-PROJECT-23591192, KAKENHI-PROJECT-24390265
  • [Journal Article] Maintenance therapy with mycophenolate mofetil after rituximab in pediatric patients with steroid-dependent nephrotic syndrome2011

    • Author(s)
      Ito S, Kamei K, Ogura M, Sato M, Fujimaru T, Ishikawa T, Udagawa T, Iijima K
    • Journal Title

      Pediatr Nephrol

      Volume: 26(10) Pages: 1823-8

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Recurrent Deep Intronic Mutations in the SLC12A3 Gene Responsible for Gitelman's Syndrome.2011

    • Author(s)
      Lo YF, Nozu K, Iijima K, Morishita T, Huang CC, Yang SS, Sytwu HK, Fang YW, Tseng MH, Lin SH.
    • Journal Title

      Clin J Am Soc Nephrol. 6(3)

      Pages: 630-639

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] The relationship between arginine vasopressin levels and hyponatremia following a percutaneous renal biopsy in children receiving hypotonic or isotonic intravenous fluids2011

    • Author(s)
      Kanda K, Nozu K, Kaito H, Iijima K, Nakanishi K, Yoshikawa N, Ninchoji T, Hashimura Y, Matsuo M, Moritz ML
    • Journal Title

      Pediatr Nephrol

      Volume: 26 Pages: 99-104

    • Data Source
      KAKENHI-PROJECT-21591396
  • [Journal Article] Recurrent EIARF and PRES with Severe Renal Hypouricemia by Compound Heterozygous SLC2A9 Mutation2011

    • Author(s)
      Shima Y, Nozu K, Nozu Y, Togawa H, Kaito H, Matsuo M, Iijima K, Nakanishi K, Yoshikawa N
    • Journal Title

      Pediatrics

      Volume: 127

    • Data Source
      KAKENHI-PROJECT-21591396
  • [Journal Article] Long-term results of a randomized controlled trial in childhood IgA nephropathy2011

    • Author(s)
      Kamei K, Nakanishi K, Ito S, Saito M, Sako M, Ishikura K, Hataya H, Honda M, Iijima K, Yoshikawa N; Japanese Pediatric IgA Nephropathy Treatment Study Group
    • Journal Title

      Clin J Am Soc Nephrol

      Volume: 6(6) Pages: 1301-7

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Japanese pediatric IgA nephropathy treatment study group. Long-term results of a randomized controlled trial in childhood IgA nephropathy2011

    • Author(s)
      Kamei K, Nakanishi K, Ito S, Saito M, Sako M, Ishikura K, Hataya H, Honda M, Iijima K, Yoshikawa N
    • Journal Title

      Clin J Am Soc Nephrol

      Volume: 6 Pages: 1301-1307

    • Data Source
      KAKENHI-PROJECT-21591396
  • [Journal Article] Molecular analysis of TSC2/PKD1 contiguous gene deletion syndrome2011

    • Author(s)
      Oyazato Y, Iijima K, Emi M, Sekine T, Kamei K, Takanashi J, Nakao H, Namai Y, Nozu K, Matsuo M
    • Journal Title

      Kobe J Med Sci.

      Volume: 57(1)

    • NAID

      110009587766

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] CAKUTに対する治療戦略 CAKUTと遺伝子変異2011

    • Author(s)
      飯島一誠
    • Journal Title

      日本小児腎不全学会雑誌

      Volume: 31 Pages: 9-10

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Epithelial-to-mesenchymal transition in cyst lining epithelial cells in an orthologous PCK rat model of autosomal-recessive polycystic kidney disease2011

    • Author(s)
      Togawa H, Nakanishi K, Mukaiyama H, Hama T, Shima Y, Sako M, Miyajima M, Nozu K, Nishii K, Nagao S, Takahashi H, Iijima K, Yoshikawa N
    • Journal Title

      Am J Physiol Renal Physiol

      Volume: 300

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] The relationship between arginine vasopressin levels and hyponatremia following a percutaneous renal biopsy in children receiving hypotonic or isotonic intravenous fluids2011

    • Author(s)
      Kanda K, Nozu K, Kaito H, Iijima K, Nakanishi K, Yoshikawa N, Ninchoji T, Hashimura Y, Matsuo M, Moritz ML
    • Journal Title

      Pediatr Nephrol

      Volume: 26 Issue: 1 Pages: 99-104

    • DOI

      10.1007/s00467-010-1647-2

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Epithelial-to-mesenchymal transition in cyst lining epithelial cells in an orthologous PCK rat model of autosomal-recessive polycystic kidney disease2011

    • Author(s)
      Togawa H, Nakanishi K, Mukaiyama H, Hama T, Shima Y, Sako M, Miyajima M, Nozu K, Nishii K, Nagao S, Takahashi H, Iijima K, Yoshikawa N
    • Journal Title

      Am J Physiol Renal Physiol

      Volume: 300 Issue: 2 Pages: F511-F520

    • DOI

      10.1152/ajprenal.00038.2010

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Treatment strategies for Henoch-Schönlein purpura nephritis by histological and clinical severity2011

    • Author(s)
      Ninchoji T, Kaito H, Nozu K, Hashimura Y, Kanda K, Kamioka I, Shima Y, Hamahira K, Nakanishi K, Tanaka R, Yoshikawa N, Iijima K, Matsuo M
    • Journal Title

      Pediatr Nephrol

      Volume: 26(4) Pages: 563-9

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Recurrent EIARF and PRES with severe renal hypouricemia by compound heterozygous SLC2A9 mutation2011

    • Author(s)
      Shima Y, Nozu K, Nozu Y, Togawa H, Kaito H, Matsuo M, Iijima K, Nakanishi K, Yoshikawa N
    • Journal Title

      Pediatrics

      Volume: 127(6)

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Identification of FOXP3-negative regulatory T-like (CD4(+)CD25(+)CD127(low)) cells in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome2011

    • Author(s)
      Otsubo K, Kanegane H, Kamachi Y, Kobayashi I, Tsuge I, Imaizumi M, Sasahara Y, Hayakawa A, Nozu K, Iijima K, Ito S, Horikawa R, Nagai Y, Takatsu K, Mori H, Ochs HD, Miyawaki T
    • Journal Title

      Clin Immunol

      Volume: 141(1) Pages: 111-20

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] A surviving case of papillorenal syndrome with the phenotype of Potter sequence2011

    • Author(s)
      Fujioka K, Morioka I, Nozu K, Nishimoto M, Amano M, Tagami M, Honda S, Yokoyama N, Yamada H, Iijima K, Matsuo M
    • Journal Title

      Pediatr Int.

      Volume: 53(3) Pages: 406-8

    • NAID

      10029558611

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Recurrent Deep Intronic Mutations in the SLC12A3 Gene Responsible for Gitelman's Syndrome2011

    • Author(s)
      Lo YF, Nozu K, Iijima K, Morishita T, Huang CC, Yang SS, Sytwu HK, Fang YW, Tseng MH, Lin SH
    • Journal Title

      Clin J Am Soc Nephrol

      Volume: 6 Issue: 3 Pages: 630-639

    • DOI

      10.2215/cjn.06730810

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Disappearance of glomerular IgA deposits in childhood IgA nephropathy showing diffuse mesangial proliferation after 2 years of combination/prednisolone therapy2011

    • Author(s)
      Shima Y, Nakanishi K, Kamei K, Togawa H, Nozu K, Tanaka R, Sasaki S, Iijima K, Yoshikawa N
    • Journal Title

      Nephrol Dial Transplant

      Volume: 26 Issue: 1 Pages: 163-169

    • DOI

      10.1093/ndt/gfq387

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Age, gender, and body length effects on reference serum creatinine levels determined by an enzymatic method in Japanese children : a multicenter study2011

    • Author(s)
      Uemura O, Honda M, Matsuyama T, Ishikura K, Hataya H, Yata N, Nagai T, Ikezumi Y, Fujita N, Ito S, Iijima K, Kitagawa T
    • Journal Title

      Clin Exp Nephrol

      Volume: 15(5) Pages: 694-9

    • NAID

      10030341017

    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] Preoperative dialysis for liver transplantation in methylmalonic acidemia2011

    • Author(s)
      Kamei K, Ito S, Shigeta T, Sakamoto S, Fukuda A, Horikawa R, Saito O, Muguruma T, Nakagawa S, Iijima K, Kasahara M
    • Journal Title

      Ther Apher Dial

      Volume: 15 Issue: 5 Pages: 488-492

    • DOI

      10.1111/j.1744-9987.2011.00974.x

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Journal Article] 小児におけるイヌリンクリアランス測定法の確立とシスタチンCによる糸球体濾過量推定式の作成2010

    • Author(s)
      亀井宏一, 伊藤秀一, 飯島一誠
    • Journal Title

      日本小児科学会雑誌

      Volume: 114 Pages: 1701-1707

    • NAID

      10027695349

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 腎臓内科学 難治性ネフローゼ症候群に対するリツキシマブ治療2010

    • Author(s)
      飯島一誠
    • Journal Title

      医学のあゆみ

      Volume: 233 Pages: 316-317

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Japanese study group of renal disease in children. Treatment with microemulsified cyclosporine in children with frequently relapsing nephrotic syndrome2010

    • Author(s)
      Ishikura K, Yoshikawa N, Hattori S, Sasaki S, Iijima K, Nakanishi K, Matsuyama T, Yata N, Ando T, Honda M
    • Journal Title

      Nephrol Dial Transplant

      Volume: 25 Pages: 3956-3962

    • Data Source
      KAKENHI-PROJECT-21591396
  • [Journal Article] Branchio-oto-renal syndrome caused by partial EYA1 deletion due to LINE-1 insertion2010

    • Author(s)
      Morisada N, Rendtorff ND, Nozu K, Morishita T, Miyakawa T, Matsumoto T, Hisano S, Iijima K, Tranebjaerg L, Shirahata A, Matsuo M, Kusuhara K.
    • Journal Title

      Pediatr Nephrol

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies2010

    • Author(s)
      Nozu K, Iijima K, Kanda K, Nakanishi K, Yoshikawa N, Satomura K, Kaito H, Hashimura Y, Ninchoji T, Komatsu H, Kamei K, Miyashita R, Kugo M, Ohashi H, Yamazaki H, Mabe H, Otsubo A, Igarashi T, Matsuo M
    • Journal Title

      J Clin Endocrinol Metab

      Volume: 95

    • Data Source
      KAKENHI-PROJECT-21591396
  • [Journal Article]2010

    • Author(s)
      中山真紀子, 野津寛大, 飯島一誠
    • Journal Title

      TCF2遺伝子異常と先天性腎尿路奇形『Annual Review 腎臓2010』(御手洗哲也・東原英二編)(中外医学社)

      Pages: 212-218

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Successful treatment of collapsing focal segmental glomerulosclerosis with a combination of rituximab, steroids and ciclosporin2010

    • Author(s)
      Kaito H, Kamei K, Kikuchi E, Ogura M, Matsuoka K, Nagata M, Iijima K, Ito S
    • Journal Title

      Pediatr Nephrol

      Volume: 25 Pages: 957-959

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] HNF1B Alterations Associated with Congenital Anomalies of the Kidney and Urinary Tract.2010

    • Author(s)
      Nakayama M, Nozu K, Goto Y, Kamei K, Ito S, Sato H, Emi M, Nakanishi K, Tuchiya S, Iijima K.
    • Journal Title

      Pediatr Nephrol 25(6)

      Pages: 1073-1079

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies.2010

    • Author(s)
      Nozu K, Iijima K, Kanda K, Nakanishi K, Yoshikawa N, Satomura K, Kaito H, Hashimura Y, Ninchoji T, Komatsu H, Kamei K, Miyashita R, Kugo M, Ohashi H, Yamazaki H, Mabe H, Otsubo A, Igarashi T, Matsuo M.
    • Journal Title

      J Clin Endocrinol Metab. 95(12)

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 【小児の治療指針】腎・尿路ステロイド感受性ネフローゼ症候群2010

    • Author(s)
      飯島一誠
    • Journal Title

      小児科診療

      Volume: 73 Pages: 691-693

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Branchio-oto-renal syndrome caused by partial EYA1 deletion due to LINE-1 insertion2010

    • Author(s)
      Morisada N, Rendtorff ND, Nozu K, Morishita T, Miyakawa T, Matsumoto T, Hisano S, Iijima K, Tranebjaerg L, Shirahata A, Matsuo M, Kusuhara K
    • Journal Title

      Pediatr Nephrol

      Volume: 25 Pages: 1343-1348

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Rituximab in refractory nephrotic syndrome2010

    • Author(s)
      Prytula A, Iijima K, Kamei K, Geary D, Gottlich E, Majeed A, Taylor M, Marks SD, Tuchman S, Camilla R, Ognjanovic M, Filler G, Smith G, Tullua K.
    • Journal Title

      Pediatr Nephrol 25

      Pages: 461-468

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 【小児の治療指針】腎・尿路ステロイド抵抗性ネフローゼ症候群2010

    • Author(s)
      飯島一誠
    • Journal Title

      小児科診療

      Volume: 73 Pages: 694-696

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Rituximab in refractory nephrotic syndrome2010

    • Author(s)
      Prytula A, Iijima K, Kamei K, Geary D, Gottlich E, Majeed A, Taylor M, Marks SD, Tuchman S, Camilla R, Ognjanovic M, Filler G, Smith G, Tullus K
    • Journal Title

      Pediatr Nephrol

      Volume: 25 Pages: 461-468

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 【難治性ネフローゼ症候群】遺伝子異常に起因するネフローゼ症候群2010

    • Author(s)
      飯島一誠, 塚口裕康
    • Journal Title

      日本腎臓学会誌

      Volume: 52 Pages: 914-923

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 高血圧で発症した高安動脈炎の三小児例2010

    • Author(s)
      宇田川智宏, 小椋雅夫, 堤晶子, 野田俊輔, 大塚泰史, 寺町昌史, 亀井宏一, 飯島一誠, 伊藤秀一
    • Journal Title

      小児高血圧研究会誌

      Volume: 7 Pages: 49-55

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] A family with X-linked benign familial hematuria2010

    • Author(s)
      Kaneko K, Tanaka S, Hasui M, Nozu K, Krol RP, Iijima K, Sugimoto K, Takemura T
    • Journal Title

      Pediatr Nephrol

      Volume: 25 Pages: 545-548

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 常染色体性Alport症候群2010

    • Author(s)
      岡政史, 野津寛大, 飯島一誠, 松尾雅文
    • Journal Title

      日本小児腎臓病学会雑誌

      Volume: 23 Pages: 8-12

    • NAID

      10026412082

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 【腎・泌尿器疾患のインフォームド・コンセントと治療選択】難治性ネフローゼ症候群FSGS小児2010

    • Author(s)
      貝藤裕史, 飯島一誠
    • Journal Title

      腎と透析

      Volume: 69 Pages: 777-780

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] HNF1B alterations associated with congenital anomalies of the kidney and urinary tract2010

    • Author(s)
      Nakayama M, Nozu K, Goto Y, Kamei K, Ito S, Sato H, Emi M, Nakanishi K, Tsuchiya S, Iijima K
    • Journal Title

      Pediatr Nephrol

      Volume: 25 Pages: 1073-79

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 運動後急性腎不全とPRES(Posterior reversible encephalopathy syndrome)の合併を反復した腎性低尿酸血症の1例2010

    • Author(s)
      島友子, 中西浩一, 戸川寛子, 野津寛大, 飯島一誠, 吉川徳茂
    • Journal Title

      日本小児腎不全学会雑誌

      Volume: 30 Pages: 145-146

    • NAID

      10027697727

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article]2010

    • Author(s)
      神田杏子, 野津寛大, 飯島一誠, 松尾雅文
    • Journal Title

      Bartter 症候群と Gitelman 症候群についての最近の知見・利尿剤負荷試験にて判明したこと『Annual Review 腎臓2010』(御手洗哲也・東原英二編)(中外医学社)

      Pages: 72-77

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 日本人小児の血清クレアチニン基準値2010

    • Author(s)
      上村治, 本田雅敬, 松山健, 秋岡祐子, 粟津緑, 飯島一誠, 池住洋平, 石倉健司, 伊藤秀一, 北山博嗣, 佐古まゆみ, 関根孝司, 永井琢人, 幡谷浩史, 藤田直也, 矢田菜穂子, 山田拓司, 日本小児腎臓病学会・小児CKD対策委員会
    • Journal Title

      日本小児腎臓病学会雑誌

      Volume: 23 Pages: 241-244

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 日本人小児(2~12歳)のGFR推算式中間報告2010

    • Author(s)
      永井琢人, 上村治, 本田雅敬, 松山健, 秋岡祐子, 粟津緑, 飯島一誠, 池住洋平, 石倉健司, 伊藤秀一, 北山博嗣, 佐古まゆみ, 関根孝司, 幡谷浩史, 藤田直也, 矢田菜穂子, 山田拓司, 日本小児腎臓病学会・小児CKD対策委員会
    • Journal Title

      日本小児腎臓病学会雑誌

      Volume: 23 Pages: 245-249

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 集学的治療により救命しえたPotter sequenceの1例2010

    • Author(s)
      忍頂寺毅史, 藤岡一路, 橋村裕也, 貝藤裕史, 森岡一朗, 野津寛大, 横山直樹, 飯島一誠, 松尾雅文
    • Journal Title

      日本小児腎不全学会雑誌

      Volume: 30 Pages: 178-180

    • NAID

      10027697824

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] ヒト常染色体劣性多発性嚢胞腎(ARPKD)相同遺伝子ラットモデル(PCKラット)の尿細管上皮細胞における上皮間葉移行(EMT)2010

    • Author(s)
      戸川寛子, 中西浩一, 島友子, 佐古まゆみ, 宮嶋正康, 野津寛大, 飯島一誠, 吉原大輔, 長尾枝澄香, 吉川徳茂
    • Journal Title

      発達腎研究会誌

      Volume: 18 Pages: 10-13

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] COL4A3/COL4A4のヘテロ接合体変異を有する菲薄基底膜腎症のドナーから生体腎移植を実施した常染色体劣性アルポート症候群の2例2010

    • Author(s)
      梶保祐子, 上田博章, 水谷誠, 谷口貴実子, 古山政幸, 石塚喜世伸, 藤井寛, 近本裕子, 秋岡祐子, 岡政史, 野津寛大, 飯島一誠, 服部元史
    • Journal Title

      日本小児腎臓病学会雑誌

      Volume: 23 Pages: 113-118

    • NAID

      130000814249

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Branchio-oto-renal syndrome caused by partial EYA1 deletion due to LINE-1 insertion.2010

    • Author(s)
      Morisada N, Rendtorff ND, Nozu K, Morishita T, Miyakawa T, Matsumoto T, Hisano S, Iijima K, Tranebjarg L, Shirahata A, Matsuo M, Kusuhara K.
    • Journal Title

      Pediatr Nephrol 25(7)

      Pages: 1343-1348

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 小児慢性腎臓病の薬物療法実態調査2010

    • Author(s)
      矢田菜穂子, 上村治, 本田雅敬, 松山健, 秋岡祐子, 粟津緑, 飯島一誠, 池住洋平, 石倉健司, 伊藤秀一, 北山浩嗣, 佐古まゆみ, 関根孝司, 永井琢人, 幡谷浩史, 藤田直也, 山田拓司, 日本小児腎臓病学会小児CKD対策小委員会
    • Journal Title

      日本小児科学会雑誌

      Volume: 114 Pages: 1631-1635

    • NAID

      10027478249

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Alport症候群と良性家族性血尿の遺伝子変異と臨床像"IV型コラーゲン関連腎症&cmp;quotという概念の提唱2010

    • Author(s)
      田中幸代, 蓮井正史, 野津寛大, 飯島一誠, 杉本圭相, 竹村司, 金子一成
    • Journal Title

      日本小児腎臓病学会雑誌

      Volume: 23 Pages: 172-178

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] HNF 1B Alterations Associated with Congenital Anomalies of the Kidney and Urinary Tract2010

    • Author(s)
      Nakayama M, Nozu K, Goto Y, Kamei K, Ito S, Sato H, Emi M, Nakanishi K, Tuchiya S, Iijima K.
    • Journal Title

      Pediatr Nephrol

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] A family with X-linked benign familial hematuria2010

    • Author(s)
      Kaneko K, Tanaka S, Hasui M, Nozu K, Krol RP, Iijima K, Sugimoto K, Takemura T.
    • Journal Title

      Pediatr Nephrol 25

      Pages: 545-548

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Severe Alport syndrome in a young woman caused by a t(X;1)(q22.3;p36.32) balanced translocation2010

    • Author(s)
      Iijima K, Nozu K, Kamei K, Nakayama M, Ito S, Matsuoka K, Ogata T, Kaito H, Nakanishi K, Matsuo M
    • Journal Title

      Pediatr Nephrol

      Volume: 25 Pages: 2165-2170

    • NAID

      120003307589

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Severe Alport syndrome in a young woman caused by a t(X;1)(q22.3;p36.32) balanced translocation.2010

    • Author(s)
      Iijima K, Nozu K, Kamei K, Nakayama M, Ito S, Matsuoka K, Ogata T, Kaito H, Nakanishi K, Matsuo M.
    • Journal Title

      Pediatr Nephrol. 25(10)

      Pages: 2165-2170

    • NAID

      120003307589

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article]2009

    • Author(s)
      野津寛大, 飯島一誠
    • Journal Title

      K[カリウム]『新しい小児の臨床検査基準値ポケットガイド』(田中敏章編)(じほう)

      Pages: 74-75

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] IPEX症候群と腎疾患2009

    • Author(s)
      橋村裕也, 野津寛大, 神田杏子, 早川晶, 竹島泰弘, 金兼弘和, 宮脇利男, 飯島一誠, 松尾雅文
    • Journal Title

      日本小児腎臓病学会雑誌 22

      Pages: 131-135

    • NAID

      10026411780

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis.2009

    • Author(s)
      Yamazaki H, Nozu K, Narita I, Nagata M, Nozu Y Fu XJ, Matsuo M, Iijima K, Gejyo F.
    • Journal Title

      Pediatr Nephrol 24

      Pages: 415-418

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] リツキシマブ投与3カ月後に無顆粒球症を呈したステロイド依存性頻回再発型ネフローゼ症候群の7歳男児例2009

    • Author(s)
      平本龍吾, 松本真輔, 江口広宣, 三好義隆, 小森功夫, 秋草文四郎, 柴田佐和子, 亀井宏一, 飯島一誠
    • Journal Title

      日本小児腎臓病学会雑誌 22

      Pages: 97-101

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Japanese study group of renal disease in children. Cyclosporine and steroid therapy in children with steroid-resistant nephrotic syndrome2009

    • Author(s)
      Hamasaki Y, Yoshikawa N, Hattori S, Sasaki S, Iijima K, Nakanishi K, Matsuyama T, Ishikura K, Yata N, Kaneko T, Honda M
    • Journal Title

      Pediatr Nephrol

      Volume: 24 Pages: 2177-2185

    • Data Source
      KAKENHI-PROJECT-21591396
  • [Journal Article] Single dose of rituximab for refractory steroid-dependent nephrotic syndrome in children2009

    • Author(s)
      Kamei K, Ito S, Nozu K, Fujinaga S, Nakayama M, Sako M, Saito M, Yoneko M, Iijima K.
    • Journal Title

      Pediatr Nephrol 24

      Pages: 1321-1328

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Increased chymase-positive mast cells in children with crescentic glomerulonephritis2009

    • Author(s)
      Togawa H, Nakanishi K, Shima Y, Obana M, Sako M, Nozu K, Tanaka R, Iijima K, Yoshikawa N
    • Journal Title

      Pediatr Nephrol

      Volume: 24 Pages: 1071-1075

    • Data Source
      KAKENHI-PROJECT-21591396
  • [Journal Article]2009

    • Author(s)
      飯島一誠
    • Journal Title

      TP【総蛋白質】『新しい小児の臨床検査基準値ポケットガイド』(田中敏章編)(じほう)

      Pages: 34-35

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 偽性低アルドステロン症I型2009

    • Author(s)
      神田杏子, 野津寛大, 橋村裕也, 飯島一誠, 松尾雅文
    • Journal Title

      日本小児腎臓病学会雑誌 22

      Pages: 123-125

    • NAID

      10026411765

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Detection by multiplex ligation-dependent probe amplification of large deletion mutations in the COL4A5 gene in female patients with Alport syndrome2009

    • Author(s)
      Nozu K, Krol RP, Nakanishi K, Yoshikawa N, Nozu Y, Ohtsuka Y, Iijima K, Matsuo M
    • Journal Title

      Pediatr Nephrol

      Volume: 24 Pages: 1773-1774

    • Data Source
      KAKENHI-PROJECT-21591396
  • [Journal Article] A deep intronic mutation in the SLC12A3 gene leads to gitelman syndrome2009

    • Author(s)
      Nozu K, Iijima K, Nozu Y, Ikegami E, Imai T, Fu XJ, Kaito H, Nakanishi K, Yoshikawa N, Matsuo M
    • Journal Title

      Pediatr Res

      Volume: 66 Pages: 590-593

    • Data Source
      KAKENHI-PROJECT-21591396
  • [Journal Article] In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation2009

    • Author(s)
      Nozu. K, Iijima. K, Kawai. K, Nozu. Y, Nishuda. A, Takeshima. Y, Fu. X. J, Hashimura. Y, Kaito. H, Nakanishi. K, Yoshikawa. N, Matsuo M
    • Journal Title

      Hum Genet

      Volume: 126 Pages: 533-538

    • Data Source
      KAKENHI-PROJECT-21591396
  • [Journal Article]2009

    • Author(s)
      野津寛大, 飯島一誠
    • Journal Title

      Cl[クロール]『新しい小児の臨床検査基準値ポケットガイド』(田中敏章編)(じほう)

      Pages: 72-73

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Increased chymase-positive mast cells in children with crescentic glomerulonephritis.2009

    • Author(s)
      Togawa H, Nakanishi K, Shim a Y, Obana M, Sako M, Nozu K, Tanaka R, Iiiima K, Yoshikawa N.
    • Journal Title

      Pediatr Nephrol (印刷中)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 【分子標的治療】分子標的治療薬を用いた治療法の現状と問題点難治性ネフローゼ症候群2009

    • Author(s)
      飯島一誠
    • Journal Title

      小児科 50

      Pages: 2021-2028

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Cyclosporine and steroid therapy in children with steroid-resistant nephrotic syndrome2009

    • Author(s)
      Hamasaki Y, Yoshikawa N, Hattori S, Sasaki S, Iijima K, Nakanishi K, Matsuyama T, Ishikura K, Yata N, Kaneko T, Honda M., Japanese Study Group of Renal Disease
    • Journal Title

      Pediatr Nephrol 24

      Pages: 2177-2185

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] A deep intronic mutation in the SLC12A3 gene leads to Gitelman syndrome2009

    • Author(s)
      Nozu K, Iijima K, Nozu Y, Ikegami E, Imai T, Fu XJ, Kaito H, Nakanishi K, Yoshikawa N, Matsuo M.
    • Journal Title

      Pediatr Res 66

      Pages: 590-593

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 運動後急性腎不全(ALPE)を呈しPRES(Posterior Reversible Encephalopathy Syndrome)を合併した腎性低尿酸血症の1例2009

    • Author(s)
      島友子, 中西浩一, 渋田昌一, 戸川寛子, 尾鼻美奈, 野津寛大, 貝藤裕史, 飯島一誠, 吉川徳茂
    • Journal Title

      日本小児腎不全学会雑誌 29

      Pages: 120-121

    • NAID

      10027866043

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation2009

    • Author(s)
      Nozu K, Iijima K, Kawai K, Nozu Y, Nishida A, Takeshima Y, Fu XJ, Hashimura Y, Kaito H, Nakanishi K, Yoshikawa N, Matsuo M.
    • Journal Title

      Hum Genet 126

      Pages: 533-538

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome2009

    • Author(s)
      Hashimura Y, Nozu K, Kanegane H, Miyawaki T, Hayakawa A, Yoshikawa N, Nakanishi K, Takemoto M, Iijima K, Matsuo M
    • Journal Title

      Pediatr Nephrol

      Volume: 24 Pages: 1181-1186

    • Data Source
      KAKENHI-PROJECT-21591396
  • [Journal Article] Detection by multiplex ligation-dependent probe amplification of largedeletion mutations in the COL4A5 gene in female patients with Alportsyndrome.2009

    • Author(s)
      Nozu K, Krol RP Nakanishi K, Yoshikawa N, Nozu Y, Ohtsuka Y, Iijima K, Matsuo M.
    • Journal Title

      Pediatr Nephrol (印刷中)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article]2009

    • Author(s)
      飯島一誠
    • Journal Title

      小児の血管性紫斑病(アレルギー性紫斑病, アナフィラクトイド紫斑病, ヘノッホ・シェーンライン紫斑病)『今日の治療指針 私はこう治療している』(山口徹・北原光夫・福井次矢編)(医学書院)

      Pages: 1117-1118

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article]2009

    • Author(s)
      野津寛大, 飯島一誠
    • Journal Title

      Na[ナトリウム]『新しい小児の臨床検査基準値ポケットガイド』(田中敏章編)(じほう)

      Pages: 70-71

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene.2009

    • Author(s)
      Kanda K, Nozu K, Yokoyama N, Morioka I, Miwa A, Hashimura Y, Kaito H, Iijima K, Matsuo M.
    • Journal Title

      BMC Nephrol 14

      Pages: 10-37

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Efficacy and safety of lisinopril for mild childhood IgA nephropathy : a pilot study2009

    • Author(s)
      Nakanishi K, Iijima K, Ishikura K, Hataya H, Awazu M, Sako M, Honda M, Yoshikawa N.
    • Journal Title

      Pediatr Nephrol 24

      Pages: 845-849

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Increased chymase-positive mast cells in children with crescentic glomerulonephritis2009

    • Author(s)
      Togawa H, Nakanishi K, Shima Y, Obana M, Sako M, Nozu K, Tanaka R, Iijima K, Yoshikawa N.
    • Journal Title

      Pediatr Nephrol 24

      Pages: 1071-1075

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation.2009

    • Author(s)
      Nozu K, Iijima K, Kawai K, Nozu Y, Nishida A, Takeshima Y, Fu XJ, Hashimura Y, Kaito H, Nakanishi K, Yoshikawa N, Matsuo M.
    • Journal Title

      Hum Genet 126(4)

      Pages: 533-538

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 溶血性尿毒症症候群発症8年後より高度蛋白尿を呈し、糸球体硬化および著明な間質の線維化を認めた1例2009

    • Author(s)
      橋村裕也, 野津寛大, 忍頂寺毅史, 貝藤裕史, 中西浩一, 吉川徳茂, 飯島一誠, 松尾雅文
    • Journal Title

      日本小児腎臓病学会雑誌 22

      Pages: 183-187

    • NAID

      10026411977

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article]2009

    • Author(s)
      飯島一誠
    • Journal Title

      難治性ネフローゼ症候群へのリツキシマブ療法『ここまできた注目の小児科臨床ガイド 小児科専門医のための生涯教育ナビゲータ』(日本小児科学会教育委員会)

      Pages: 130-136

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome2009

    • Author(s)
      Hashimura Y, Nozu K, Kanegane H, Miyawaki T, Hayakawa A, Yoshikawa N, Nakanishi K, Takemoto M, Iijima K, Matsuo M.
    • Journal Title

      Pediatr Nephrol 24

      Pages: 1181-1186

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] A deep intronic mutation in the SLC12A3 gene leads to Gitelman syndrome.2009

    • Author(s)
      Nozu K, Iijima K, Nozu Y, Ikegami E, Imai T, Fu XJ, Kaito H, Nakanishi K, Yoshikawa N, Matsuo M.
    • Journal Title

      Pediatr Res 66(5)

      Pages: 590-593

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Efficacy and safety of lisinopril for mild childhood IgA nephropathy : apilot study.2009

    • Author(s)
      Nakanishi K, Iijima K, Ishikura K, Hataya H, Awazu M, Sako M, Honda M, Yoshikawa N ; for the Japanese Pediatric IgA Nephropathy Treatment Study Group.
    • Journal Title

      Pediatr Nephrol 24

      Pages: 845-849

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article]2009

    • Author(s)
      飯島一誠
    • Journal Title

      ALB[アルブミン]『新しい小児の臨床検査基準値ポケットガイド』(田中敏章編)(じほう)

      Pages: 36-37

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Membranous nephropathy associated with thyroid-peroxidase antigen.2009

    • Author(s)
      Shima Y, Nakanishi K, Togawa H, Obana M, Sako M, Miyawaki M, Nozu K, Iijima K, Yoshikawa N.
    • Journal Title

      Pediatr Nephrol 24

      Pages: 605-608

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Successful treatment of collapsing focal segmental glomerulosclerosis with a combination of rituximab, steroids and cicloaporin2009

    • Author(s)
      Kaito H, Kamei K, Kikuchi E, Ogura M, Matsuoka K, Nagata M, Iijima K, Ito S.
    • Journal Title

      Pediatr Nephrol

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 小児期ネフローゼ症候群の特徴2009

    • Author(s)
      飯島一誠
    • Journal Title

      日本内科学会雑誌 98

      Pages: 998-1004

    • NAID

      10024934586

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.2009

    • Author(s)
      Hashimura Y, Nozu K, Kanegane H, Miyawaki T, Hayakawa A, Yoshikawa N, Nakanishi K, Takemoto M, Iijima K, Matsuo M.
    • Journal Title

      Pediatr Nephrol 24(6)

      Pages: 1181-1186

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis.2009

    • Author(s)
      Yamazaki H, Nozu K, Narita I, Nagata M, Nozu Y, Fu XJ, Matsuo M, Iijima K, Gejyo F.
    • Journal Title

      Pediatr Nephrol 24(2)

      Pages: 415-418

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene2009

    • Author(s)
      Kanda K, Nozu K, Yokoyama N, Morioka I, Miwa A, Hashimura Y, Kaito H, Iijima K, Matsuo M.
    • Journal Title

      BMC Nephrol 10

      Pages: 37-37

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Membranous nephropathy associated with thyroid-peroxidase antigen2009

    • Author(s)
      Shima Y, Nakanishi K, Togawa H, Obana M, Sako M, Miyawaki M, Nozu K, Iijima K, Yoshikawa N
    • Journal Title

      Pediatr Nephrol

      Volume: 24 Pages: 605-608

    • Data Source
      KAKENHI-PROJECT-21591396
  • [Journal Article] 生体腎移植直後に再発したが、寛解導入しえたFSGSの5歳女児例2009

    • Author(s)
      白川利彦, 亀井宏一, 伊藤秀一, 松岡健太郎, 佐古まゆみ, 島友子, 中西浩一, 長田道夫, 吉川徳茂, 飯島一誠
    • Journal Title

      日本小児腎不全学会雑誌 29

      Pages: 175-178

    • NAID

      10027866166

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] 当院にて2007年以降に経験した小児献腎移植の4例2009

    • Author(s)
      兵頭洋二, 石村武志, 竹田雅, 貝藤裕史, 神田杏子, 野津寛大, 三宅秀明, 田中一志, 武中篤, 飯島一誠, 藤澤正人
    • Journal Title

      日本小児腎不全学会雑誌 29

      Pages: 198-200

    • NAID

      10027866233

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Minimal change nephrotic syndrome associated with IPEX syndrome.2009

    • Author(s)
      Hashimura Y, Nozu K, Kanegane H, Miyawaki T, Hayakawa A, Yoshikawa N, Nakanishi K, Takemoto M, Iiiima K, Matsuo M.
    • Journal Title

      Pediatr Nephrol (印刷中)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.2008

    • Author(s)
      Nozu K, Przybyslaw Krol R, Ohtsuka Y, Nakanishi K, Yoshikawa N, Nozu Y, Kaito H, Kanda K, Hashimura Y, Hamasaki Y, Iiiima K, Matsuo M.
    • Journal Title

      Pediatr Nephrol 23

      Pages: 2085-2090

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Rituximab for refractory focal segmental glomerulosclerosis2008

    • Author(s)
      Nakayama M, Kamei K, Nozu K, Matsuoka K, Nakagawa A, Sako M, Iijima K
    • Journal Title

      Pediatr Nephrol 23

      Pages: 481-485

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness2008

    • Author(s)
      Nozu K, Inagaki T, Fu XJ, Nozu Y, Kaito H, Kanda K, Sekine T, Igarashi T,Nakanishi K, Yoshikawa N, Iijima K, Matsuo M.
    • Journal Title

      J Med Genet 45

      Pages: 182-186

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Management of diarrhea-associated hemolytic uremic syndronne in children2008

    • Author(s)
      Iijima K, Kamioka I, Nozu K
    • Journal Title

      Clin Exp Nephrol 12

      Pages: 16-19

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness.2008

    • Author(s)
      Nozu K, Inagaki T, Fu XJ, Nozu Y, Kaito H, Kanda K, Sekine T, Igarashi T, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M.
    • Journal Title

      J Med Genet 45

      Pages: 182-186

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Management of diarrhea-associated hemolytic uremic syndrome in children2008

    • Author(s)
      Iijima K, Kamioka I, Nozu K
    • Journal Title

      Clin Exp Nephrol 12

      Pages: 16-19

    • NAID

      10025351663

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Rituximab for refractory focal segmental glomerulosclerosis2008

    • Author(s)
      Nakayama M, Kamei K, Nozu K, Matsuoka K, Nakagawa A, Sako M, Iijima K.
    • Journal Title

      Pediatr Nephrol 23

      Pages: 481-485

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Steroid-resistant nephrotic syndrome.2008

    • Author(s)
      Kitamura A, Tsukaguchi H, Maruyama K, Shono A, Iijima K, Kagami S, Doi T.
    • Journal Title

      Kidney Int. 74(9)

      Pages: 1209-1215

    • NAID

      40017118263

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Rituximab for refractory focal segmeltal glomerulosclerosis2008

    • Author(s)
      Nakayama M, Kamei K, NozuK, Matsuoka K, Nakagawa A, Sako M.Iijima K
    • Journal Title

      Pediatr Nephrol 23

      Pages: 481-485

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome.2008

    • Author(s)
      Krol RP, Nozu K, Nakanishi K, Iijima K, Takeshima Y, Fu XJ, Nozu Y, Kaito H, Kanda K, Matsuo M, Yoshikawa N.
    • Journal Title

      Nephrol Dial Transplant. 23(8)

      Pages: 2525-3250

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Steroid-resistant nephrotic syndrome.2008

    • Author(s)
      Kitamura A, Tsukaguchi H, Maruyama K, Shono A, Iijima K, Kagami s, Doi T.
    • Journal Title

      Kidney Int 74

      Pages: 1209-1215

    • NAID

      40017118263

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Improved renal survival in Japanese children with IgA nephropathy.2008

    • Author(s)
      Yata N, Nakanishi K, Shima Y, Togawa H, Obana M, Sako M, Nozu K, Tanaka R, Iijima K, Yoshikawa N
    • Journal Title

      Pediatr Nephrol 23

      Pages: 905-912

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Combination therapy with mizoribine for severe childhood IgA nephropathy : a pilot study.2008

    • Author(s)
      Yoshikawa N, Nakanishi K, Ishikura K, Hataya H, Iijima K, Honda M; Japanese Pediatric IgA Nephropathy Treatment Study Group
    • Journal Title

      Pediatr Nephrol 23

      Pages: 757-763

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Molecular analysis of digenic inheritance in Bartter syndrome with sens orineural deafness2008

    • Author(s)
      Nozu K, Inagaki T, Fu XJ, Nozu Y, Kaito H, Kalda K, SekileT, Igarashi T, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M
    • Journal Title

      J Med Genet 45

      Pages: 182-186

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Management of diarrhea-associated hemolytic uremic syndrome in children2008

    • Author(s)
      Iijima K, Kamioka I, Nozu K.
    • Journal Title

      Clin Exp Nephrol 12

      Pages: 16-19

    • NAID

      10025351663

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.2008

    • Author(s)
      Nozu K, Przybyslaw Krol R, Ohtsuka Y, Nakanishi K, Yoshikawa N, Nozu Y, Kaito H, Kanda K, Hashimura Y, Hamasaki Y, Iijima K, Matsuo M.
    • Journal Title

      Pediatr Nephrol. 23(11)

      Pages: 2085-2090

    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Risk factors for developing severe clinical course in HUS patients : a national survey in Japan.2008

    • Author(s)
      Kamioka I, Yoshiya K, Satomura K, Kaito H, Fujita T, Iijima K, Nakanishi K, Yoshikawa N, Nozu K, Matsuo M; Japanese Society for Pediatric Nephrology.
    • Journal Title

      Pediatr Int 50

      Pages: 441-446

    • NAID

      10025344153

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Effective and safe treatment with cyclosporine in nephrotic children : aprospective, randomized multicenter trial.2008

    • Author(s)
      Ishikura K, Ikeda M, Hattori S, Yoshikawa N, Sasaki S, Iijima K, Nakanishi K, Yata N, Honda M.
    • Journal Title

      Kidney Int 73

      Pages: 1167-1173

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness2008

    • Author(s)
      Nozu K, Inagaki T, Fu XJ, Nozu Y, Kaito H, Kanda K, Sekine T, Igarashi T, Nakanishi K, Yoshikawa N, Iijima K, Matuo M
    • Journal Title

      J Med Genet 45

      Pages: 182-186

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome.2008

    • Author(s)
      Krol RP, Nozu K, Nakanishi K, Iiiima K, Takeshima Y, Fu XJ, Nozu Y, Kaito H, Kanda K, Matsuo M, Yoshikawa N.
    • Journal Title

      Nephrol Dial Transplant 23

      Pages: 2525-2530

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Proglosis and pathological characteristics of five children with non-Shiga toxin-mediated hemolytic uremic syndrome2007

    • Author(s)
      Kamioka I, Nozu K, Fujita T, Kaito H, Talaka R, Ybshiya K, Iijima K, Nakanishi K, Yoshikawa N, Matsuo M
    • Journal Title

      Pediatr Int 49

      Pages: 196-201

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] A familial childhood-onset relapsing nephrotic syndrome2007

    • Author(s)
      Kitamura A, Tsukaguchi H, Hiramoto R, Shono A, Doi T, Kagami S, Iijima K
    • Journal Title

      Kidney Int 71

      Pages: 946-951

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Prognosis and pathological characteristics of five children with non-Shiga toxin-mediated hemolytic uremic syndrome2007

    • Author(s)
      Kamioka I, Nozu K, Fujita T, Kaito H, Tanaka R, Yoshiya K, Iijima K, Nakanishi K, Yoshikawa N, Matsuo M
    • Journal Title

      Pediatr Int 49

      Pages: 196-201

    • NAID

      10019494531

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Long-term follow-up of juvenile acute nonproliferative glomerulitis (JANG).2007

    • Author(s)
      Fujita T, Nozu K, Iijima K, Kamioka I, Kaito H, Tanaka R, Nakanishi K, Matsuo M, Yoshikawa N
    • Journal Title

      Pediatr Nephrol 22

      Pages: 1957-1961

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] OCRL1 mutations in patients with Dent disease phenotype in Japan2007

    • Author(s)
      Sekine T, Nozu K, Iyengar R, Fu XJ, Matsuo M, Tanaka R, Iijima K, Matsui E, Harita Y, Inatomi J, Igarashi T
    • Journal Title

      Pediatr Nephrol 22

      Pages: 975-980

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Association of cumulative cyclosporine dose with its irreversible nephrotoxicity in Japanese patients with pediatric-onset autoimmune diseases2007

    • Author(s)
      Nakamura T, Nozu K, Iijima K, Yoshikawa N, Moriya Y, Yamamori M, Kako A, Matsuo M, Sakurai A, Okamura K, Sakaeda T
    • Journal Title

      Biol Pharm Bull 30

      Pages: 2371-2375

    • NAID

      110006546441

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Long-term follow up of juvenile acute nonproliferative glomerulitis(JANG)2007

    • Author(s)
      Fujita T, Nozu K Iijima K, Kamioka I, Kaito H, Tanaka R, Nakanishi K,Matsuo M, Yoshikawa N.
    • Journal Title

      Pediatr Nephrol 22

      Pages: 1957-1961

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Association of cumulative cyclosporine dose with its hrreversible nephrotoxicity il Japalese patients with pediatric-olset autoimmule diSeases2007

    • Author(s)
      Nakamura T, Nozu K, Iijima K, Yoshikawa N, Moriya Y, Yamamori M, Kako A, Matsuo M, Sakurai A, Okamura N, IshikawaT, Okumura K, Sakaeda T
    • Journal Title

      Biol Pharm Bull 30

      Pages: 2371-2375

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Chronic glomerulonephritis associated with IgG subclass deficiency2007

    • Author(s)
      Kamei K, Nakagawa A, Otsuka Y, Nakayama M, Kobayashi S, Matsuoka K, Iijima K
    • Journal Title

      Pediatr Nephrol 22

      Pages: 1229-1234

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Chronic glomerulonephritis associated with IgG subclasS deficiency2007

    • Author(s)
      Kamei K, Nakagawa A, Otsuka Y, Nakayama M, Kobayashi S, Matsuoka K, Iijima K
    • Journal Title

      Pediatr Nephrol 22

      Pages: 1229-1234

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Long-term follow-up of juvenile acute nonproliferative glomeruhtis(JANG)2007

    • Author(s)
      Fujita T, Nozu K, Iijima K, Kamioka I, Kaito H, Talaka R, Nakanishi K, Matsuo M, Yoshikawa N
    • Journal Title

      Pediatr Nephrol 22

      Pages: 1957-1961

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] A novel mutation in KCNJ1n a Bartter syndrome case diagnosed as pseudohypoaldosteronism2007

    • Author(s)
      Nozu K, Fu XJ, Kaito H, Kanda K, Yokoyama N, Przybyslaw Krol R, Nakajima T, Kajiyama M, Iijima K, Matsuo M.
    • Journal Title

      Pediatr Nephrol 22

      Pages: 1219-1223

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Molecular analysis of patients with type III Bartter syndrome: picking up large heterozygous deletions with semiquantitative PCR2007

    • Author(s)
      Nozu K, Fu XJ, Nakanishi K, Yoshikawa N, Kaito H, Kanda K, Krol RP, Miyashita R, Kamitsuji H, Kanda S, Hayashi Y, Satomura K, Simizu N, Iijima K, Matsuo M
    • Journal Title

      Pediatr Res 62

      Pages: 364-369

    • NAID

      10025701181

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Detection of a transcript ablormahty il mRNA of the SLC12A3 gene extracted from urinary sedimelt cells of a patient with Gitelman's syndrome2007

    • Author(s)
      Kaito H, Nozu K, Fu XJ, Kamioka I, Fujita T, Kalda K, Krol RP, Sumi-aga R, Ishida A, Iijima K, Matsuo M
    • Journal Title

      Pediatr Res 61

      Pages: 502-506

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Association of cumulative cyclosporine dose with its irreversible nephrotoxicity in Japanese patients with pediatric-onset autoimmune diseases2007

    • Author(s)
      Nakamura T, Nozu K., Iijima K, Yoshikawa N, Moriya Y, Yamamori M,Kako A, Matsuo M, Sakurai A, Okamura N, Isktkawa T, Okumura K,Sakaeda T.
    • Journal Title

      Biol Pharm Bull 30

      Pages: 2371-2375

    • NAID

      110006546441

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronisnn2007

    • Author(s)
      Nozu K, Fu XJ, Kaito H, KandaK, Yokoyama N, Przybyslaw Krol R, Nakajima T, Kajiyama M, Iijima K, Matsuo M
    • Journal Title

      Pediatr Nephrol 22

      Pages: 1219-1223

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Chronic glomerulonephritis associated with IgG subclass deficiency2007

    • Author(s)
      Kamei K, Nakagawa A, Otsuka Y, Nakayama M, Kobayashi S, Matsuoka K, Iijima K.
    • Journal Title

      Pediatr Nephrol 22

      Pages: 1229-1234

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Molecular analysis of patients with type III Bartter syndrome:pickingup large heterozygous deletions with semiquantitative PCR2007

    • Author(s)
      Nozu K, Fu XJ, Nakanishi K, Yoshikawa N, Kaito H, Kalda K, Krol RP, Miyashita R, Kamitsuji H, Kalda S, Hayashi Y, Satomura K, Shimizu N, Iijima K, Matsuo M
    • Journal Title

      Pediatr Res 62

      Pages: 364-369

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome2007

    • Author(s)
      Kaito H, Nozu K, Fu XJ, Kamioka I, Fujita T, Kanda K, Krol RP, Suminaga R, Ishida A, Iijima K, Matsuo M
    • Journal Title

      Pediatr Res 61

      Pages: 502-506

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] OCRLI mutations in patients with Dent disease phenotype in Japar2007

    • Author(s)
      Sekine T, Nozu K, Iyengar R, FuXJ, Matsuo M, Tanaka R, Iijima K, Matsui E, Harita Y, Inatomi J, Igarashi T
    • Journal Title

      Pediatr Nephrol 22

      Pages: 975-980

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome.2007

    • Author(s)
      Kaito H, Nozu K, Fu XJ, Kanda K, Krol RP, Suminaga R, Ishida A, Iijima K, Matsuo M
    • Journal Title

      Pediatr Res 61(4)

      Pages: 502-525

    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism2007

    • Author(s)
      Nozu K, Fu XJ, Kaito H, Kanda K, Yokoyama N, Przybyslaw Krol R, Nakajima T, Kajiyama M, Iijima K, Matsuo M
    • Journal Title

      Pediatr Nephrol 22

      Pages: 1219-1223

    • NAID

      120000943595

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Molecular analysis of patients with type III Bartter syndrome : picking up large heterozygous deletions with semiquantitative PCR2007

    • Author(s)
      Nozu K, Fu XJ, Nakanishi K, Yoshikawa N, Kaito H, Kanda K, Krol RP, Miyashita R, Kamitsuji H, Kanda S, Hayashi Y, Satomura K, Shimizu N, Iijima K, Matsuo M.
    • Journal Title

      Pediatr Res 62

      Pages: 364-369

    • NAID

      10025701181

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome2007

    • Author(s)
      Kaito H, Nozu K, Fu XJ, Kamioka I, Fujita T, Kanda K, Krol RP, Summaga R, Ishida A, Iijima K, Matsuo M.
    • Journal Title

      Pediatr Res 61

      Pages: 502-506

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] OCRL1 mutations in patients with Dent disease phenotype in Japan2007

    • Author(s)
      Sekine T, Nozu K, Iyengar R, Fu XJ, Matsuo M, Tanaka R, Iijima K, Matsui E, Harita Y, Inatomi J, Igarashi T.
    • Journal Title

      Pediatr Nephrol 22

      Pages: 975-980

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] A familial childhood-onset relapsing nephritic syndrome.2007

    • Author(s)
      Kitamura A, Tsukaguchi H, Hiramoto R, Shono A, Doi T, Kagami S, Iijima K
    • Journal Title

      Kidney Int 71(9)

      Pages: 946-951

    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] A familial childhood-onset relapsing nephrotic syndrome2007

    • Author(s)
      Kitamura A, Tsukaguchi H, Hiramoto R, Shono A, Doi T, Kagami S, Iijima K
    • Journal Title

      Kidney Int 17

      Pages: 946-951

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Prognosis and pathological characteristics of five children with non-Shiga toxin-mediated hemolytic uremic syndrome2007

    • Author(s)
      Kaimoka I, Nozu K, Fujita T, Kaito H, Tanaka R, Yoshiya K, Iijima K, Nakanishi K, Yoshikawa N, Matsuo M.
    • Journal Title

      Pediatr Int 49

      Pages: 196-201

    • NAID

      10019494531

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Prediction of systemic exposure to cyclosporine in Japanese pediatric patients.2006

    • Author(s)
      Sakaeda T, Iijima K, Nozu K, Nakamura T, Moriya Y, Nishikawa M, Wada A, Okamura N, Matsuo M, Okumura K
    • Journal Title

      J Hum Gen 51(11)

      Pages: 969-976

    • NAID

      40015182076

    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Segmental membranous glomerulonephritis in children : comparison with global membranous glomerulonephritis.2006

    • Author(s)
      Obana M, Nakanishi K, Sako M, Yata N, Nozu K, Tanaka R, Iijima K, Yoshikawa N
    • Journal Title

      Clin J Am Soc Nephrol 1(4)

      Pages: 723-729

    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] The effect of aldosterone blockade in patients with Alport syndrome.2006

    • Author(s)
      Kaito, H., Nozu, K., Kanda, K., Przybyslaw, KR., Nakanishi, K., Yoshiya, K., Iijima, K., Yoshikawa, N., Matsuo, M
    • Journal Title

      Pediatr Nephrol 21(12)

      Pages: 1824-1829

    • NAID

      120000943596

    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Mechanisms of Development and Progression of Cyanotic Nephropathy2006

    • Author(s)
      Inatomi J, Matsuoka K, Fujimaru R, Nakagawa A, Iijima K
    • Journal Title

      Pediatr Nephrol 21(10)

      Pages: 1440-1445

    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Enamel-renal syndrome associated with hypokalemic metabolic alkalosis and impaired renal concentration : a novel syndrome?2006

    • Author(s)
      Fu XJ, Nozu, K, Goji, K, Ikeda, K, Kamioka, K, Fujita, T, Kaito, H, Nishino, H, Iijima, K, Matsuno, M
    • Journal Title

      Nephrol Dial Transplant 21(10)

      Pages: 2959-2962

    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Genetics and Clinical Features of 15 Asian Families with Steroid- Resistant Nephrotic Syndrome.2006

    • Author(s)
      Kitamura A, Tuskaguchi H, Iijima K, Araki J, Hattori M, Ikeda M, Honda M, Nozu K, Nakazato H, Yoshikawa N, Kagami S, Muramatsu M, Choi Y, Cheong HI, Doi T
    • Journal Title

      Nephrol Dial Transplant 21(11)

      Pages: 3133-3138

    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Molecular Mechanism for Proteinuria in Recurrent Nephrotic Syndrome.2006

    • Author(s)
      Tsukaguchi H, Iijima K.
    • Journal Title

      Annual Review 2006 Kidney (Chugai Igaku (Tokyo)) 74-80

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16390245
  • [Journal Article] Steroid treatment for severe childhood IgA nephropathy : a randomized controlled trial.2006

    • Author(s)
      Yoshiwaka N, Honda M, Iijima K, Awazu M, Hattori S, Nakanishi K, Ito H, for the Japanese Pediatric IgA Nephropathy Treatment Study Group
    • Journal Title

      Clin J Am Soc Nephrol 1(3)

      Pages: 511-517

    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Strategy and recent progression of human genetic study for nephrotic syndrome.2005

    • Author(s)
      Tsukaguchi H, Iijima K..
    • Journal Title

      Kidney and Dialysis 59

      Pages: 82-89

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16390245
  • [Journal Article] ネフローゼ症候群の責任遺伝子の探索、研究方法と動向2005

    • Author(s)
      塚口 裕康, 飯島一誠
    • Journal Title

      腎と透析 59

      Pages: 82-89

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16390245
  • [Journal Article] Glomerulosclerosis and gene mutations2005

    • Author(s)
      Iijima K, Tsukaguchi H.
    • Journal Title

      Kidney and Dialysis 59

      Pages: 124-128

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16390245
  • [Journal Article] 遺伝子異常に伴う糸球体硬化2005

    • Author(s)
      飯島一誠, 塚口 裕康
    • Journal Title

      腎と透析 59

      Pages: 124-128

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16390245
  • [Journal Article] A New Clinical Entity of Fragile Silt Membrane Nephrotic Syndrome in Which NPHS1 Variants Serve as a Predisposing Factor for Proteinuria.2005

    • Author(s)
      Kitamura A, Iijima K, Tsukaguchi H, Hiramoto R, Shono A, Choi Y, Cheong HI, Doi T, Kagami S.
    • Journal Title

      J Am Soc Nephrol 16

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16390245
  • [Journal Article] Steroid Resintant Nephrotic Syndrome

    • Author(s)
      Kitamura A, Tsukaguchi H, Maruyama K, Shono A, Iijima K, Kagami S, Doi T.
    • Journal Title

      Kidney Int (in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Improved renal survival in Japanese children with IgA nephropathy

    • Author(s)
      Yata N, Nakanishi K, Shima Y, Togawa H, Obana M, Sako M, Nozu K, Tanaka R, Iijima K, Yoshikawa N.
    • Journal Title

      Pediatr Nephrol (in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Steroido Resintant Nephrotic Syndrome

    • Author(s)
      Kitamura A, Tsukaguchi H, Maruyama K, Shono A, Iijima K, Kagami S, Doi T,
    • Journal Title

      Kidney Int (印刷中)

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Severe Alport syndrome in a female caused by a t(X;1)(q22.3;p36.32)balanced translocation

    • Author(s)
      Iijima K, Nozu K, Kamei K, Nakayama K, Ito S, Natsuoka K, Ogata T, Kaito H, Nakanishi K, Matsuo M.
    • Journal Title

      Pediatr Nephrol (In press(掲載確定))

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Journal Article] Improved renal survival in Japanese children with IgA nephropathy

    • Author(s)
      Yata N, Nakanishi K, Shima Y, Togawa H, Obana M, Sako M, Nozu K, Tanaka R, Iijima K, Yoshikawa N
    • Journal Title

      Pediatr Nephrol (印刷中)

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome

    • Author(s)
      Krol RP, Nozu K, Nakanishi K, Iijima K, Takeshima Y, Fu XJ, Nozu Y, Kaito H, Kanda K, Matsuo M, Yoshikawa N.
    • Journal Title

      Nephrol Dial Transplant (in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome

    • Author(s)
      Krol RP, Nozu K, Nakanishi K, Iijima K, Takeshima Y, Fu XJ, Nozu Y, Kaito H, Kanda K, Matsuo M, Yoshikawa N
    • Journal Title

      Nephrol Dial Transplant (印刷中)

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Steroid Resintant Nephrotic Syndrome

    • Author(s)
      Kitamura A, Tsukaguchi H, Maruyama K, Shono A, Iijima K, K agami S.Doi T
    • Journal Title

      Kidley Int (印刷中)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome

    • Author(s)
      Krol RP, Nozu K, Nakanishi K, Iijima K, Takeshhma Y, Fu XJ, Nozu Y, Kaito H, Kanda K, Matsuo M, Yoshikawa N
    • Journal Title

      Nephrol Dial Transplant (印刷中)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Journal Article] Improved renal survival in Japanese childrel with IgA nephropathy

    • Author(s)
      Yata N, Nakanishi K, Shima Y, Togawa H, Obala M, Sako M, Nozu K, Tanak:a R, Iijima K, Yoshikawa N
    • Journal Title

      Pediatr Nephrol (印刷中)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] MMF after rituximab for complicated FRNS/SDNS2022

    • Author(s)
      Kazumoto Iijima
    • Organizer
      19th Congress of the International Pediatric Nephrology Association
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-21KK0147
  • [Presentation] MMF after rituximab for complicated FRNS/SDNS2022

    • Author(s)
      Kazumoto Iijima
    • Organizer
      19th Congress of the International Pediatric Nephrology Association
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H03698
  • [Presentation] State of the art nephrotic syndrome: Insights into pathogenesis and treatment2022

    • Author(s)
      Kazumoto Iijima
    • Organizer
      54th Annual Scientific Meeting of the European Society for Pediatric Nephrology
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H03698
  • [Presentation] State of the art nephrotic syndrome: Insights into pathogenesis and treatment2022

    • Author(s)
      Kazumoto Iijima
    • Organizer
      54th Annual Scientific Meeting of the European Society for Pediatric Nephrology
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-21KK0147
  • [Presentation] エビデンスに基づいた小児ネフローゼ症候群の治療2021

    • Author(s)
      飯島一誠
    • Organizer
      第42回日本小児腎不全学会学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-20H03698
  • [Presentation] エビデンスに基づいた小児ネフローゼ症候群の治療2021

    • Author(s)
      飯島一誠
    • Organizer
      第42回日本小児腎不全学会学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-21KK0147
  • [Presentation] 小児腎臓疾患の今と昔-小児ネフローゼ症候群の病院探索研究および治療開発研究UP TO DATE-2021

    • Author(s)
      飯島一誠
    • Organizer
      第55回日本小児腎臓病学会
    • Invited
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Presentation] 小児ネフローゼ症候群の病因探索研究および治療開発研究 UP TO Date2021

    • Author(s)
      飯島一誠、野津寛大、佐古まゆみ
    • Organizer
      第55回日本小児腎臓病学会学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-20H03698
  • [Presentation] 小児ネフローゼ症候群の治療法開発と病因探索研究の最前線2020

    • Author(s)
      飯島一誠
    • Organizer
      第50回日本腎臓学会東部学術大会
    • Invited
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Presentation] 遺伝性腎疾患に対するプレシジョンメディスン アルポート症候群に対する遺伝子標的療法の開発2019

    • Author(s)
      野津寛大、山村智彦、飯島一誠
    • Organizer
      第54回日本小児腎臓病学会学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] 常染色体劣性Alport症候群39家系46人の臨床遺伝学的検討2019

    • Author(s)
      堀之内智子、野津寛大、榊原菜々、長野智那、南川将吾、山村智彦、飯島一誠
    • Organizer
      第62回日本腎臓学会学術集会
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] 遺伝性腎疾患に対するプレシジョンメデイスン 小児ステロイド感受性ネフローゼ症候群の疾患感受性遺伝子2019

    • Author(s)
      飯島一誠、 Jia Xiaoyuan,、山村智彦、人見祐基、長野智那、堀之内智子、野津寛大、徳永勝士
    • Organizer
      第54回日本小児腎臓病学会学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Presentation] Alport症候群モデルマウスにおけるエクソンスキッピング療法の有効性の検討2019

    • Author(s)
      山村智彦、野津寛大、堀之内智子、南川将吾、 足立朝美、寺川真紀、永瀬弘之、高石巨澄、 大西朗之、小路貴生、小泉誠、神田祥一郎、 張田豊、嘉村美里、甲斐広文、飯島一誠
    • Organizer
      第54回日本小児腎臓病学会学術集会
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] 遺伝性ネフローゼ症候群における臨床的特徴の検討2019

    • Author(s)
      長野智那、野津寛大、青砥悠哉、石河慎也、榊原菜々、南川将吾、山村智彦、飯島一誠
    • Organizer
      第54回日本小児腎臓病学会学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Presentation] Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome2019

    • Author(s)
      Tomoko Horinouchi, Tomohiko Yamamura, Rasheed A. Gbadegesin, Matthew G. Sampson, China Nagano, Kandai Nozu, Kenji Ishikura, Pierre M. Ronco, Hae Il Cheong, Kazumoto Iijima
    • Organizer
      American Society of Nephrology Kidney week 2019
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Presentation] Exon skipping therapy for COL4A5 gene truncating variant rescued progression of kidney failure in X-linked Alport syndrome2019

    • Author(s)
      Tomohiko Yamamura, Kandai Nozu, Kazumoto Iijima
    • Organizer
      American Society of Nephrology Kidney week 2019
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] NPHS1は小児ステロイド感受性ネフローゼ症候群の疾患感受性遺伝子である2019

    • Author(s)
      山村智彦、長野智那、堀之内智子、 野津寛大、飯島一誠
    • Organizer
      第62回日本腎臓学会学術集会
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Presentation] 先天性/乳児および ステロイド抵抗性ネフローゼ症候群における網羅的遺伝子診断2019

    • Author(s)
      長野智那、野津寛大、青砥悠哉、石河慎也、榊原菜々、南川将吾、山村智彦、飯島一誠
    • Organizer
      第122回日本小児科学会学術集会
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Presentation] 常染色体劣性Alport症候群39家系46人の臨床遺伝学的検討2019

    • Author(s)
      堀之内智子、野津寛大、石河慎也、青砥悠哉、 榊原菜々、長野智那、南川将吾、山村智彦、 貝藤裕史、森貞直哉、飯島一誠
    • Organizer
      第54回日本小児腎臓病学会学術集会
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] Factors regulating the severity in male X-linked Alport syndrome: study of 367 cases2018

    • Author(s)
      Yamamura T, Nozu K, Sakakibara N, Nagano C, Fujimura J, Horinouchi T, Nakanishi K, Minamikawa S, Kaito H, Shima Y, Nakanishi K, Iijima K
    • Organizer
      52st Annual Meeting of the American Society of Nephrology
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] 次世代シークエンサーを用いたAlport症候群の網羅的診断法の確立2018

    • Author(s)
      山村 智彦、野津 寛大、長野 智那、榊原 菜々、藤村 順也、堀之内 智子、中西 啓太、南川 将吾、貝藤 裕史、飯島 一誠
    • Organizer
      第121回日本小児科学会学術集会
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] ゲノムワイド関連解析による小児特発性ネフローゼ症候群のrisk haplotype同定2018

    • Author(s)
      堀之内 智子、野津 寛大、石倉 健司、飯島 一誠
    • Organizer
      第61回日本腎臓学会学術総会
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Presentation] ネフローゼ症候群の病因としての遺伝子異常2018

    • Author(s)
      野津 寛大、中西 啓太、飯島 一誠
    • Organizer
      第53回小児腎臓病学会学術集会
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Presentation] ゲノムワイド関連解析による小児特発性ネフローゼ症候群のrisk haplotype同定2018

    • Author(s)
      堀之内 智子、Xiaoyuan Jia、人見 祐基、石倉 健司、亀井 宏一、濱田 陸、郭 義胤、藤丸 季可、岡本 孝之、大和田 葉子、田中 亮二郎、後藤 芳充、貝籐 裕史、野津 寛大、徳永 勝士、飯島 一誠
    • Organizer
      第53回小児腎臓病学会学術集会
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Presentation] X染色体連鎖型Alport症候群男性患者341名の臨床遺伝学的検討2018

    • Author(s)
      山村 智彦、野津 寛大、榊原 菜々、長野 智那、藤村 順也、堀之内 智子、中西 啓太、南川 将吾、貝藤 裕史、中西 浩一、飯島 一誠
    • Organizer
      第61回日本腎臓学会学術総会
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] カレント・トピック4 小児腎疾患における遺伝医学のトピックス2018

    • Author(s)
      飯島一誠
    • Organizer
      日本人類遺伝学会第63回大会
    • Invited
    • Data Source
      KAKENHI-PROJECT-18KK0244
  • [Presentation] Genotype-phenotype correlation in male X-linked Alport syndrome: 341 cases study2018

    • Author(s)
      Yamamura T, Sakakibara N, Nagano C, Nozu K, Fujimura J, Horinouchi T, Nakanishi K, Minamikawa S, Kaito H, Iijima K
    • Organizer
      第53回小児腎臓病学会学術集会
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] カレント・トピック4 小児腎疾患における遺伝医学のトピックス2018

    • Author(s)
      飯島一誠
    • Organizer
      日本人類遺伝学会第63回大会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] Splicing assay with hybrid minigene: assessing pathogenicities in COL4A5 intronic mutations2018

    • Author(s)
      Horinouchi T, Nozu K, Yamamura T, Sakakibara N, Nagano C, Nakanishi K, Fujimura J, Minamikawa S, Ninchoji T, Kaito H, Shima Y, Nakanishi K, Iijima K
    • Organizer
      52st Annual Meeting of the American Society of Nephrology
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] 海綿状血管腫を合併した鰓弓耳腎(Branchio-oto-renal)症候群の1例2017

    • Author(s)
      岩城拓磨、近藤健夫、小西行彦、福家典子、郡司朗子、岡田 仁、日下 隆、若林誉幸、森貞直哉、飯島一誠
    • Organizer
      第52回日本小児腎臓病学会学術集会
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 未診断疾患における網羅的ゲノム解析時代の遺伝カウンセリング 小児CKD(慢性腎臓病)の原因遺伝子解析と遺伝カウンセリング2017

    • Author(s)
      森貞直哉、野津寛大、飯島一誠
    • Organizer
      第41回日本遺伝カウンセリング学会学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 尿細管機能異常と電解質2017

    • Author(s)
      野津寛大
    • Organizer
      第7回東北小児内分泌講演会
    • Invited
    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Presentation] 次世代シークエンサーを用いたAlport症候群の網羅的診断法の確立2017

    • Author(s)
      山村智彦、野津寛大、藤村順也、堀之内智子、中西啓太、南川将吾、庄野朱美、忍頂寺毅史、貝藤裕史、中西浩一、飯島一誠
    • Organizer
      第60回日本腎臓学会 仙台
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] OFD1ヘミ接合性ミスセンス変異を認めたネフロン癆関連シリオパチーの1男児例2017

    • Author(s)
      清水順也、森貞直哉、飯島一誠、神農陽子、城 謙輔、竹村 司、久保俊英、塚原宏一
    • Organizer
      第52回日本小児腎臓病学会学術集会
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 腎病理所見にて髄質嚢胞腎(MCKD)の特徴を認めた2例2017

    • Author(s)
      岡田絵里、川口武彦、森維久郎、山田亜純、上原正樹、岡島真里、山川貴史、首村守俊、北村博司、森貞直哉、野津寛大、今澤俊之
    • Organizer
      第47回日本腎臓学会東部学術大会
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] エクソンスキッピング療法によるアルポート症候群特異的療法治療法の開発2017

    • Author(s)
      庄野朱美、野津寛大、小泉 誠、大西朗之、高石巨澄、山村智彦、南川将吾、飯島一誠
    • Organizer
      第52回日本小児腎臓病学会 東京
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] Establishment of a comprehensive diagnostic method using next generation sequencer for the Alport syndrome2017

    • Author(s)
      Yamamura T, Nozu K, Fujimura J, Horinouchi T, Nakanishi K, Manamikawa S, Shono A, Ninchoji T, Kaito H, Nakanishi K, Iijima K
    • Organizer
      第52回日本小児腎臓病学会 東京
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] EYA1遺伝子欠損による鰓弓耳腎症候群の1例2017

    • Author(s)
      岩重洋平、伊東悠貴、嘉藤光歩、大棟浩平、杉谷盛太、前沢浩司、東義人、森貞直哉、野津寛大、飯島一誠
    • Organizer
      第47回日本腎臓学会西部学術大会
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] A comprehensive diagnosis by targeted sequencing for clinically suspectsd alport syndrome patients in Japan2017

    • Author(s)
      Yamamura T, Nozu K, Fujimura J, Horinouchi T, Nakanishi K, Minamikawa S, Shono A, Ninchoji T, Kaito H, Shima Y, Nakanishi K, Iijima K.
    • Organizer
      Asian Congress of Pediatric Nephrology 2017 & 39th Malaysian Pediatric Association Annual Congress, Kuala Lumpur, Malaysia
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H04189
  • [Presentation] OFD1ヘミ接合性変異を認めたネフロン癆関連シリオパチーの1男児例2017

    • Author(s)
      森貞直哉、清水順也、庄野朱美、野津寛大、飯島一誠
    • Organizer
      第271回 日本小児科学会兵庫県地方会
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 次世代シークエンサーを用いたAlport症候群の網羅的診断法の確立2017

    • Author(s)
      山村智彦、野津寛大、藤村順也、堀之内智子、中西啓太、南川将吾、庄野朱美、忍頂寺毅史、貝藤裕史、中西浩一、飯島一誠
    • Organizer
      第60回日本腎臓学会 仙台
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] Comprehensive analysis using target sequencing panel for congenital anomalies of the kidney and urinary tract and nephronophthisis in Japan2017

    • Author(s)
      Naoya Morisada, Akemi Shono, Kandai Nozu, Ryojiro Tanaka, Kazumoto Iijima
    • Organizer
      American society of Human Genetics 2017
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] A comprehensive diagnosis by targeted sequencing for clinically suspectsd alport syndrome patients in Japan2017

    • Author(s)
      Yamamura T, Nozu K, Fujimura J, Horinouchi T, Nakanishi K, Minamikawa S, Shono A, Ninchoji T, Kaito H, Shima Y, Nakanishi K, Iijima K.
    • Organizer
      Asian Congress of Pediatric Nephrology 2017 & 39th Malaysian Pediatric Association Annual Congress, Kuala Lumpur, Malaysia
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] 遺伝性腎疾患の研究から学んだ大切なこと-研究の楽しさと臨床へのフィードバック-2017

    • Author(s)
      野津寛大
    • Organizer
      第120回日本小児科学会学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Presentation] NGSターゲット遺伝子シークエンスパネルによるCAKUTおよびNPHの包括的原因遺伝子解析2017

    • Author(s)
      森貞直哉、庄野朱美、野津寛大、忍頂寺毅史、叶 明娟、井藤奈央子、神田祥一郎、亀井宏一、石倉健司、伊藤秀一、山本勝輔、塚口裕康、里村憲一、田中亮二郎、飯島一誠
    • Organizer
      第52回日本小児腎臓病学会学術集会
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] エクソンスキッピング療法によるアルポート症候群特異的療法治療法の開発2017

    • Author(s)
      庄野朱美、野津寛大、小泉 誠、大西朗之、高石巨澄、山村智彦、南川将吾、飯島一誠
    • Organizer
      第52回日本小児腎臓病学会 東京
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] Establishment of a comprehensive diagnostic method using next generation sequencer for the Alport syndrome2017

    • Author(s)
      Yamamura T, Nozu K, Fujimura J, Horinouchi T, Nakanishi K, Manamikawa S, Shono A, Ninchoji T, Kaito H, Nakanishi K, Iijima K
    • Organizer
      第52回日本小児腎臓病学会 東京
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] NPH・MCKDの遺伝子診断と病型2017

    • Author(s)
      森貞直哉、野津寛大、飯島一誠
    • Organizer
      第60回日本腎臓学会学術総会
    • Invited
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 家族内検索が有用であった腎コロボーマ症候群の一家系2017

    • Author(s)
      溝端理恵、大塚泰史、陣内久美子、大串栄彦、岡 政史、佐藤忠司、青木茂久、森貞直哉、叶 明娟、飯島一誠、松尾宗明
    • Organizer
      第52回日本小児腎臓病学会学術集会
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 出生前に常染色体劣性多発性嚢胞腎と画像診断され遺伝子診断を行った2症例2017

    • Author(s)
      金井麻子、武藤はる香、林 周作、金川武司、岡本陽子、石井桂介、光田信明、岡本伸彦、森貞直哉、飯島一誠
    • Organizer
      第41回日本遺伝カウンセリング学会学術集会
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 3歳時に蛋白尿を契機に発見されたmulticentric carpotarsal osteolysis syndromeの1例2017

    • Author(s)
      白鳥孝俊、稲熊洋祐、中川 拓、神田杏子、森貞直哉、飯島一誠、田中亮二郎
    • Organizer
      第52回日本小児腎臓病学会学術集会
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 原因遺伝子が同定された稀少ネフロン癆関連シリオパチー症例の検討2017

    • Author(s)
      森貞直哉、叶 明娟、庄野朱美、野津寛大、飯島一誠
    • Organizer
      第62回日本人類遺伝学会
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] Clinical Diagnosis of Senior Loken Syndrome in a Patient with SDCCAG8 Mutation Genetically Diagnosed as Having Bardet-Biedle Syndrome2017

    • Author(s)
      Yuko Fujii, Hiroshi Tamai, Akira Ashida, Hideki Matsumura, Akihiko Shirasu, Satoshi Yamazaki, Hyogo Nakakura, Naoya Morisada, Kazumoto Iijima, Motoshi Hattori
    • Organizer
      Kidney Week (American Society of Nephrology) 2017
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] NGSターゲット遺伝子シークエンスパネルによるCAKUTおよびNPHの包括的原因遺伝子解析2017

    • Author(s)
      森貞直哉、庄野朱美、野津寛大、忍頂寺毅史、田中亮二郎、飯島一誠
    • Organizer
      第60回日本腎臓学会学術総会
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 遺伝性腎疾患2016

    • Author(s)
      野津寛大, 森貞直哉, 飯島一誠
    • Organizer
      第59回日本腎臓学会学術総会
    • Place of Presentation
      パシフィコ横浜(神奈川県横浜市)
    • Year and Date
      2016-06-17
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] PAX2変異のある先天性腎尿路奇形に合併した後腹膜成熟奇形腫にectopic immature renal tissueを認めた一例2016

    • Author(s)
      菅原典子, 永野千代子, 稲垣徹史, 森貞直哉, 野津寛大, 飯島一誠
    • Organizer
      第46回日本腎臓学会東部学術大会
    • Place of Presentation
      京王プラザホテル(東京都新宿区)
    • Year and Date
      2016-10-07
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] Genetic and clinical characteristics of female X-linked Alport Syndrome: 267case study2016

    • Author(s)
      Yamamura T, Nozu K, Nakanishi K, Horinouchi T, Fujimura J, Minamikawa S, Kamiyoshi N, Ninchoji T, Kaito H, Morisada N, Nakanishi K, Yoshikawa N, Iijima K
    • Organizer
      17th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      RAFAIN PALACE HOTEL & CONVENTION (Iguazu, Brazil)
    • Year and Date
      2016-09-20
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] Rare nephronophthisis related ciliopathy identified by next generation sequencing in ten non-consanguineous families2016

    • Author(s)
      Naoya Morisada, Akemi Shono, Kandai Nozu, Takeshi Ninchoji, Koji Nagatani, Toshiyuki Ohta, Junya Shimizu, Takahisa Yoshikawa, Ken Saida, Shingo Ishimori, Masato Yasui, China Nagano, Koichi Kamei, Kenji Ishikura, Shuichi Ito, Ryojiro Tanaka, Kazumoto Iijima
    • Organizer
      American Society of Human Genetics 2016
    • Place of Presentation
      Vancouver (Canada)
    • Year and Date
      2016-10-18
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 左後腹膜成熟奇形腫にEctopic immature renal tissueを伴った左無形成腎・右低形成 腎の一例2016

    • Author(s)
      菅原典子,永野千代子,安藤 亮,遠藤尚文,佐藤智樹,高橋立子,手塚文明,稲垣徹史,佐藤 篤,森貞直哉,野津寛大,飯島一誠
    • Organizer
      第51回日本小児腎臓病学会学術集会
    • Place of Presentation
      ウインクあいち(愛知県名古屋市)
    • Year and Date
      2016-07-07
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 特発性ネフローゼ症候群の成因と治療2016

    • Author(s)
      野津寛大
    • Organizer
      第52回日本小児腎臓病学会学術集会
    • Place of Presentation
      名古屋
    • Year and Date
      2016-07-07
    • Invited
    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Presentation] 男女共同参画委員会企画:遺伝性腎疾患2016

    • Author(s)
      野津寛大, 森貞直哉, 飯島一誠
    • Organizer
      第59回日本腎臓学会学術総会
    • Place of Presentation
      パシフィコ横浜(横浜)
    • Year and Date
      2016-06-17
    • Invited
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] ネフローゼ症候群と遺伝子-どこまで分かっているか、どのような場合遺伝子診断が必要か2016

    • Author(s)
      野津寛大
    • Organizer
      第52回日本小児腎臓病学会学術集会
    • Place of Presentation
      名古屋
    • Year and Date
      2016-07-07
    • Invited
    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Presentation] Gene targeting therapy for Alport syndrome2016

    • Author(s)
      Kandai Nozu
    • Organizer
      2016 Pediatric Academic Societies Meeting
    • Place of Presentation
      Baltimore
    • Year and Date
      2016-05-02
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Presentation] 次世代シークエンサーによる稀少ネフロン癆関連シリオパチーの原因遺伝子解析2016

    • Author(s)
      森貞直哉,野津寛大,庄野朱美,忍頂寺毅史,田中亮二郎,飯島一誠
    • Organizer
      第39回日本小児遺伝学会
    • Place of Presentation
      慶應義塾大学三田北館ホールと会議室(東京)
    • Year and Date
      2016-12-09
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 平滑筋腫を合併したアルポート症候群の臨床 像と遺伝学的検討2016

    • Author(s)
      南川 将吾, 野津 寛大, 中西 啓太, 藤村 順也, 堀之内 智子, 神吉 直宙, 忍頂寺 毅史, 長野 智那, 後藤 芳充, 平野 大志, 藤永 周一郎, 高橋 英彦, 森下 高弘, 森貞直哉, 田村 雅仁, 飯島 一誠
    • Organizer
      第51回日本小児腎臓病学会学術集会
    • Place of Presentation
      ウインクあいち(愛知県名古屋市)
    • Year and Date
      2016-07-07
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] ネフロン発生にかかわる遺伝子とその腎外での役割と異常の検出方法2016

    • Author(s)
      森貞直哉, 飯島一誠
    • Organizer
      第59回日本腎臓学会学術総会
    • Place of Presentation
      パシフィコ横浜(神奈川県横浜市)
    • Year and Date
      2016-06-17
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 次世代シークエンサーによる染色体優性Alport症候群診断法の確立2016

    • Author(s)
      神吉 直宙, 野津 寛大, 中西 啓太, 堀之内 智子, 藤村 順也, 南川 将吾, 山村 智彦 松野下夏樹, 忍頂寺毅史, 飯島一誠
    • Organizer
      第119回日本小児科学会学術集会
    • Place of Presentation
      ロイトン札幌(札幌)
    • Year and Date
      2016-05-13
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] 次世代シークエンサー(NGS)による染色体優性Alport症候群診断法の確立および臨床的、病理学的検討2016

    • Author(s)
      山村智彦, 野津寛大, 南川将吾, 神吉直宙, 忍頂寺毅史, 飯島一誠
    • Organizer
      第59回日本腎臓学会学術総会
    • Place of Presentation
      パシフィコ横浜(横浜)
    • Year and Date
      2016-06-17
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] 偽性バーター症候群を呈し次世代シークエン サーによりPAX2遺伝子変異が同定された 腎低異形成の1女児例2016

    • Author(s)
      波多江健, 慶田裕美, 檜山麻衣子, 黒木理恵, 黒川麻里, 山中一郎, 森貞直哉, 野津寛大, 飯島一誠
    • Organizer
      第51回日本小児腎臓病学会学術集会
    • Place of Presentation
      ウインクあいち(愛知県名古屋市)
    • Year and Date
      2016-07-07
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] X染色体連鎖型Alport症候群女性267例の遺伝学的・臨床的検討2016

    • Author(s)
      山村智彦, 野津寛大, 中西啓太, 堀之内智子, 藤村順也, 南川将吾, 神吉直宙, 忍頂寺毅史, 貝藤裕史, 森貞直哉, 中西浩一, 吉川徳茂, 飯島一誠
    • Organizer
      第51回日本小児腎臓病学会学術集会
    • Place of Presentation
      ウインクあいち(名古屋)
    • Year and Date
      2016-07-07
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] X染色体連鎖型Alport症候群女性267例 の遺伝学的・臨床的検討2016

    • Author(s)
      山村 智彦, 野津 寛大, 中西 啓太, 堀之内 智子, 藤村 順也, 南川 将吾, 神吉 直宙, 忍頂寺 毅史, 貝藤 裕史, 森貞 直哉, 中西 浩一, 吉川 徳茂, 飯島 一誠
    • Organizer
      第51回日本小児腎臓病学会学術集会
    • Place of Presentation
      ウインクあいち(愛知県名古屋市)
    • Year and Date
      2016-07-07
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 頻回の尿路感染症を契機に子宮膀胱瘻の診断に至ったHDR (hypoparathyroidism, deafness, renal dysplasia)症候群の1例2016

    • Author(s)
      富井祐治,神田祥一朗,森貞直哉,滝澤慶一,笹田洋平,薮内智朗,金子直人,佐藤泰征,石塚喜世伸,近本裕子,秋岡祐子,三浦健一郎,飯島一誠,服部元史
    • Organizer
      第51回日本小児腎臓病学会学術集会
    • Place of Presentation
      ウインクあいち(愛知県名古屋市)
    • Year and Date
      2016-07-07
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 頻回の尿路感染症を契機に子宮膀胱瘻の診断に至ったHDR症候群の1例2016

    • Author(s)
      富井祐治,神田祥一朗,森貞直哉,滝澤慶一,笹田洋平,薮内智朗,金子直人,佐藤泰征,石塚喜世伸,近本裕子,秋岡祐子,三浦健一郎,飯島一誠,服部元史
    • Organizer
      第46回日本腎臓学会東部学術大会
    • Place of Presentation
      京王プラザホテル(東京都新宿区)
    • Year and Date
      2016-10-07
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 次世代シークエンサーにて診断に至った SDCCAG8変異によるネフロン虜の女児例2016

    • Author(s)
      中西 啓太, 忍頂寺毅史, 藤村順也, 堀之内智子, 南川将吾, 山村智彦, 神吉直宙, 石森真吾, 野津寛大, 森貞直哉, 飯島一誠
    • Organizer
      第51回日本小児腎臓病学会学術集会
    • Place of Presentation
      ウインクあいち(愛知県名古屋市)
    • Year and Date
      2016-07-07
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] The comprehensive genetic analysis of congenital anomalies of the kidney and urinary tract (CAKUT) in Japan2016

    • Author(s)
      Naoya Morisada, Akemi Shono, Mariko Taniguchi-Ikeda, Kandai Nozu, Koichi Kamei, Kenji Ishikura, Shuichi Ito, Ryojiro Tanaka, Hisahide Nishio, Kazumoto Iijima
    • Organizer
      The 13th International Congress of Human GeneticsKyoto
    • Place of Presentation
      Kyoto (Japan)
    • Year and Date
      2016-04-03
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 男女共同参画「genderと腎-遺伝性腎疾患」2016

    • Author(s)
      野津寛大、飯島一誠
    • Organizer
      第60回日本腎臓学会
    • Place of Presentation
      東京
    • Year and Date
      2016-06-18
    • Invited
    • Data Source
      KAKENHI-PROJECT-15K09691
  • [Presentation] 次世代シークエンサーによる重症心身障害者施設での原因遺伝子解析2016

    • Author(s)
      森貞 直哉, 加藤 威, 加藤 神奈, 島 亜衣, 藤田 花織, 西村 範行, 西尾 久英, 和田 博子, 飯島 一誠
    • Organizer
      第119回日本小児科学会学術集会
    • Place of Presentation
      ロイトン札幌、ホテルさっぽろ芸文館(北海道札幌市)
    • Year and Date
      2016-05-13
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] CAKUT及び原因不明の小児期発症慢性腎機能障害患者への包括的原因遺伝子解析2016

    • Author(s)
      森貞 直哉, 野津 寛大, 庄野 朱美, 忍頂寺 毅史, 叶 明娟, 井藤 奈央子, 神田 祥一郎, 亀井 宏一, 石倉 健司, 伊藤 秀一, 山本 勝輔, 里村 憲一, 服部 元史, 田中 亮二郎, 西尾 久英, 飯島 一誠
    • Organizer
      第51回日本小児腎臓病学会学術集会
    • Place of Presentation
      ウインクあいち(愛知県名古屋市)
    • Year and Date
      2016-07-07
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 女性先天性腎尿路奇形(Congenital Anomalies of the Kidney and Urinary Tract:CAKUT)患者の生殖器奇形合併について2016

    • Author(s)
      神田祥一郎、森貞直哉, 滝澤慶一, 富井祐治, 濱 浩隆, 金子直人, 薮内智朗, 中野栄治, 多田憲正, 石塚喜世伸, 近本裕子, 秋岡祐子, 三浦健一郎, 飯島一誠, 服部元史
    • Organizer
      第51回日本小児腎臓病学会学術集会
    • Place of Presentation
      ウインクあいち(愛知県名古屋市)
    • Year and Date
      2016-07-07
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] ターゲットシークエンス法による常染色体優性Alport症候群診断法の確立および遺伝学的背景、臨床的、病理学的検討2016

    • Author(s)
      神吉直宙、野津寛大、中西啓太、堀之内智子、藤村順也、南川将吾、 山村智彦、松野下夏樹、忍頂寺毅史、中西浩一、吉川徳茂、飯島一誠
    • Organizer
      第51回日本小児腎臓病学会学術集会
    • Place of Presentation
      ウインクあいち(名古屋)
    • Year and Date
      2016-07-07
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] BOR(Branchio-Oto-Renal)症候群が確定 した腎移植の1例2016

    • Author(s)
      濱 浩隆, 神田祥一郎, 森貞直哉, 熊谷直憲, 滝澤慶一, 富井祐治, 薮内智朗, 金子直人, 中野栄治, 多田憲正, 菅原典子, 石塚喜世伸, 近本裕子, 秋岡祐子, 飯島一誠, 服部元史
    • Organizer
      第51回日本小児腎臓病学会学術集会
    • Place of Presentation
      ウインクあいち(愛知県名古屋市)
    • Year and Date
      2016-07-07
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 臨床的にAlagille症候群が疑われたが次世 代シークエンサーによる解析でNPHP3遺 伝子変異を認めRHPD1と診断した1例2016

    • Author(s)
      白鳥 孝俊, 中川 拓, 神田 杏子, 叶 明娟, 森貞 直哉, 飯島 一誠, 田中 亮二郎
    • Organizer
      第51回日本小児腎臓病学会学術集会
    • Place of Presentation
      ウインクあいち(愛知県名古屋市)
    • Year and Date
      2016-07-07
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 教育講演 小児腎疾患診療における遺伝学的アプローチ2015

    • Author(s)
      飯島一誠,森貞直哉,野津寛大
    • Organizer
      第37回日本小児腎不全学会学術集会
    • Place of Presentation
      石川
    • Year and Date
      2015-11-26
    • Invited
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] 常染色体優性Alport症候群の遺伝学的背景と臨床像2015

    • Author(s)
      神吉直宙,野津寛大,南川将吾,山村智彦,松野下夏樹,大坪裕美,忍頂寺毅史,貝藤裕史,飯島一誠
    • Organizer
      第58回日本腎臓学会学術総会
    • Place of Presentation
      名古屋
    • Year and Date
      2015-06-05
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] Genetic, pathological and clinical backgrounds in autosomal dominant Alport syndrome.2015

    • Author(s)
      Nozu K, Kamiyoshi N, Matsunoshita N, Minamikawa S, Yamamura T, Ninchoji T, Tanaka R, Nakanishi K, Yoshikawa N, Iijima K.
    • Organizer
      48th Annual Scientific Meeting of the European Society for Pediatric Nephrology
    • Place of Presentation
      Square Brussels Meeting Centre (Brussels, Belgium)
    • Year and Date
      2015-09-03
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] Branchio-oto-renal(BOR)症候群の原因遺伝子と腎症状に関する検討2015

    • Author(s)
      森貞直哉、野津寛大、松永達雄、飯島一誠
    • Organizer
      第58回日本腎臓学会学術集会
    • Place of Presentation
      名古屋市
    • Year and Date
      2015-06-05
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] Genital Organ Anomalies in Female Pediatric Patients with End-Stage Renal Disease.2015

    • Author(s)
      Kanda S, Morisada N, Tomii Y,Takizawa K, Kaneko N, Yabuuchi T, Hama H, Nakano E, Tada N, Ishizuka K, Akioka Y, Chikamoto H, Iijima K, Hattori M.
    • Organizer
      Kidney Week 2015
    • Place of Presentation
      San Diego Convention Center (San Diego, U.S.A.)
    • Year and Date
      2015-11-03
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] PAX2異常を認めた腎コロボーマ症候群の2例2015

    • Author(s)
      山本 雅紀、 藤田 直也, 深山 雄大, 大前 隆志, 森貞 直哉, 飯島 一誠
    • Organizer
      第50回日本小児腎臓病学会学術集会
    • Place of Presentation
      神戸市
    • Year and Date
      2015-06-18
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] New-Onset Diabetes After Transplantation in a Pediatric Patient with Congenital Anomalies of the Kidney and Urinary Tract: The Role of Hepatocyte Nuclear Factor 1β.2015

    • Author(s)
      Kaneko N, Morisada N,Takizawa K, Yabuuchi T, Hama H,Tada N, Nakano E, Kanda S, Ishizuka K, Chikamoto H, Akioka Y, Iijima K, Hattori M.
    • Organizer
      Kidney Week 2015
    • Place of Presentation
      San Diego Convention Center (San Diego, U.S.A.)
    • Year and Date
      2015-11-03
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] よくわかるシリーズ7 小児ネフローゼ症候群の治療 リツキサン2015

    • Author(s)
      飯島一誠
    • Organizer
      第58回日本腎臓学会学術総会
    • Place of Presentation
      名古屋
    • Year and Date
      2015-06-05
    • Invited
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] 肝酵素上昇を契機にHNF1b変異が同定されたCAKUT(Congenital Anomalies of the Kidney and Urinary Tract)の1例2015

    • Author(s)
      神田 祥一郎, 森貞 直哉, 秋岡 祐子, 金子 直人, 苗代 有鈴, 薮内 智朗, 多田 憲正, 宮井 貴之, 菅原 典子, 石塚 喜世伸, 近本 裕子, 飯島 一誠, 服部 元史
    • Organizer
      第50回日本小児腎臓病学会学術集会
    • Place of Presentation
      神戸市
    • Year and Date
      2015-06-18
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] A Family Case of Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome with a Novel Mutation of GATA3.2015

    • Author(s)
      Yabuuchi T, Kanda S, Morisada N, Takizawa K, Tomii Y, Kaneko N, Hama H, Nakano E, Tada N, Ishizuka K, Chikamoto H, Akioka Y, Iijima K, Hattori M.
    • Organizer
      Kidney Week 2015
    • Place of Presentation
      San Diego Convention Center (San Diego, U.S.A.)
    • Year and Date
      2015-11-03
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] Branchio-oto-renal(BOR)症候群の原因遺伝子と腎症状に関する検討2015

    • Author(s)
      森貞直哉、野津寛大、松永達雄、飯島一誠
    • Organizer
      第50回日本小児腎臓病学会学術集会
    • Place of Presentation
      神戸市
    • Year and Date
      2015-06-18
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 会長講演 小児特発性ネフローゼ症候群-新たな治療戦略と今後の課題-2015

    • Author(s)
      飯島一誠
    • Organizer
      日本小児腎臓病学会学術集会 第50回記念大会
    • Place of Presentation
      神戸
    • Year and Date
      2015-06-18
    • Invited
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] 常染色体優性Alport症候群における遺伝学的背景および臨床的、病理学的検討2015

    • Author(s)
      神吉直宙,野津寛大,南川将吾,山村智彦,松野下夏樹,大坪裕美,忍頂寺毅史,貝藤裕史,飯島一誠
    • Organizer
      日本小児腎臓病学会学術集会 第50回記念大会
    • Place of Presentation
      神戸
    • Year and Date
      2015-06-18
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] ワークショップ1 腎炎・ネフローゼ症候群の治療トピックス 難治性ネフローゼ症候群に対するリツキシマブ治療2015

    • Author(s)
      飯島一誠,野津寛大,佐古まゆみ
    • Organizer
      第45回日本腎臓学会西部学術大会
    • Place of Presentation
      金沢
    • Year and Date
      2015-10-23
    • Invited
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] HNF1B変異が同定されたNODAT(New-Onset Diabetes After Transplantation)の1例2015

    • Author(s)
      神田祥一郎、森貞直哉、秋岡祐子、滝澤慶一、富井祐治、金子直人、薮内智朗、濱浩隆、中野栄治、多田憲正、石塚喜世伸、近本裕子、飯島一誠、服部元史
    • Organizer
      第45回日本腎臓学会東部学術大会
    • Place of Presentation
      東京都
    • Year and Date
      2015-10-02
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] 巨大腎腫大を認めた口顔指症候群1型(OFD1)の一例2015

    • Author(s)
      竹村浩至、早見典子、乳原善文、今福 礼、川田真宏、住田圭一、上野智敏、三瀬広記、平松里佳子、長谷川詠子、諏訪部達也、星野純一、澤直樹、森貞直哉、飯島一誠、高市憲明
    • Organizer
      第45回日本腎臓学会東部学術大会
    • Place of Presentation
      東京都
    • Year and Date
      2015-10-02
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] Somatic Mosaicism and Variant Frequency Detected by Next Generation Sequencing in X Linked Alport Syndrome.2015

    • Author(s)
      Kamiyoshi N, Nozu K, Fu X.J, Yamamura T, Minamikawa S, Ninchoji T, Iijima K.
    • Organizer
      Kidney Week 2015
    • Place of Presentation
      San Diego Convention Center (San Diego, U.S.A.)
    • Year and Date
      2015-11-03
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] Target gene sequencing panelを用いた先天性腎尿路奇形症候群(CAKUT)の網羅的遺伝子解析2015

    • Author(s)
      森貞直哉、庄野朱美、野津寛大、叶明娟、神田祥一郎、井藤奈央子、 亀井宏一、伊藤秀一、山本勝輔、里村憲一、西尾久英、飯島一誠
    • Organizer
      第60回日本人類遺伝学会
    • Place of Presentation
      東京都
    • Year and Date
      2015-10-14
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] Comprehensive Approach to Understand Human Renal Development Based on the Identification of Responsible Genes for CAKUT.2015

    • Author(s)
      Shono A, Morisada N, Nozu K, Iijima K.
    • Organizer
      Kidney Week 2015
    • Place of Presentation
      San Diego Convention Center (San Diego, U.S.A.)
    • Year and Date
      2015-11-03
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] 腎外症状のないNPHP1遺伝子欠失若年性ネフロン癆の2例2015

    • Author(s)
      堀 朋子, 上野 茉央, 前川 明洋, 中沢 将之, 岩崎 啓介, 早田 宏, 森貞 直哉, 飯島 一誠, 澄川 耕二, 西野 友哉
    • Organizer
      第45回日本腎臓学会西部学術大会
    • Place of Presentation
      金沢市
    • Year and Date
      2015-10-23
    • Data Source
      KAKENHI-PROJECT-15K09261
  • [Presentation] CAKUTの分子遺伝学的アプローチ2013

    • Author(s)
      飯島一誠
    • Organizer
      第22回日本小児泌尿器科学会総会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Heterozygous microdeletion of 16q covering SALL1 and RPGRIP1L could be a novel contiguous gene syndrome with renal impairment2013

    • Author(s)
      Morisada N, Taniguchi-Ikeda M, Ishimori S, Ninchoji T, Kaito H, Nozu K, Adach Mi, Takeshima Y, SekineT, Iijima K
    • Organizer
      American Society of Human Genetics
    • Place of Presentation
      Boston
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] 総排泄腔遺残をともなった1q21.1欠失症候群の1女児例2013

    • Author(s)
      森貞直哉,野田俊輔,降?めぐみ,池田真理子,竹島泰弘,飯島一誠
    • Organizer
      日本人類遺伝学会第58回大会
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] 遺伝性腎疾患の最近の知見2013

    • Author(s)
      飯島一誠
    • Organizer
      第48回日本小児腎臓病学会学術集会
    • Place of Presentation
      徳島
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Natural History and Protein Expression Pattern in Autosomal Recessive Alport Syndrome Based on the Comprehensive Strategy for Genetic Analysis2013

    • Author(s)
      Kaito H, Nozu K, Oka M, Morisada N, Ninchoji T, Nakanishi K, Yoshikawa N, Iijima K
    • Organizer
      American Society of Nephrology KIDNEY WEEK
    • Place of Presentation
      Atlanta
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Genetic approaches in pediatric nephrology.2012

    • Author(s)
      Iijima K
    • Organizer
      Japan-Korea The 10th Pediatric Nephrology Seminar 2012
    • Place of Presentation
      東京
    • Invited
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Clinicopathological characteristics and kidney outcome of childhood-onset lupus nephritis with acute kidney injury: from the multicenter study in Japan.2012

    • Author(s)
      Ishimori S, Kaito H, Otsubo H, Hashimoto F, Ninchoji T, Hashimura Y, Kamioka I, Shima Y, Hamahira K, Nakanishi K, Tanaka R, Yoshikawa N, Iijima K.
    • Organizer
      45th Annual Scientific Meeting of the European Society for Pediatric Nephrology Krakow 2012.9.6-8
    • Place of Presentation
      Krakow
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] リツキシマブ ネフローゼ症候群への応用2012

    • Author(s)
      飯島一誠,佐古まゆみ
    • Organizer
      第55回日本腎臓学会学術総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Clinical characteristics and mutational pattern of genetically-proven Gitelman’s syndrome.2012

    • Author(s)
      Ninchoji T, Kaito H, Nozu K, Nakanishi K, Yoshikawa N, Iijima K
    • Organizer
      American Society of Nephrology, 2012 Kidney Week
    • Place of Presentation
      San Diego
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] A novel UMOD mutation in a family with medullary cystic kidney disease type 2.2012

    • Author(s)
      Kamijo M, Tamura M, Ishimatsu N, Miyamoto T, Serino R, Kabashima N, Kanegae K, Furuno Y, Bando K, Nakamata J, Kuma A, Ishimori S, Morisada N, Iijima K, Otsuji Y.
    • Organizer
      American Society of Nephrology, 2012 Kidney Week
    • Place of Presentation
      San Diego
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] 小児特発性ネフローゼ症候群におけるステロイド反応性と蛍光免疫染色所見との関連2012

    • Author(s)
      忍頂寺毅史,貝藤裕史,大坪裕美,橋本総子,石森真吾,森貞直哉,吉川徳茂,飯島一誠
    • Organizer
      第47回日本小児腎臓病学会学術集会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Hyponatremic Hypertensive Syndrome in an Infant Child Presenting as Nephrotic Syndrome:2012

    • Author(s)
      Ninchoji T, Kaito H, Otsubo H, Hashimoto F, Ishimori S, Hashimura Y, Morisada N, Kawasaki A, Yamaguchi M, Iijima K.
    • Organizer
      Japan-Korea The 10th Pediatric Nephrology Seminar 2012
    • Place of Presentation
      東京
    • Invited
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Possible contribution of fibrocytes to renal fibrosis in Cpk mouse, a model of ARPKD.2012

    • Author(s)
      Hama T, Nakanishi K, Mukaiyama H, Togawa H, Shima Y, Miyajima M, Takahashi H, Nagao S, Iijima K, Yoshikawa N.
    • Organizer
      American Society of Nephrology, 2012 Kidney Week
    • Place of Presentation
      San Diego
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Genetical and clinical aspects of X-linked Alport syndrome in males with positive staining of the α5 (IV) chain.2012

    • Author(s)
      Hashimura Y, Nozu K, Kaito H, Ishimori S, Otsubo H, Hashimoto F, Ninchoji T, Morisada N, Nakanishi K, Yoshikawa N, Iijima K.
    • Organizer
      American Society of Nephrology, 2012 Kidney Week
    • Place of Presentation
      San Diego
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Multicenter double-blind, randomized, placebo-controlled trial of rituximab for the treatment of childhood-onset refractory nephrotic syndrome.2012

    • Author(s)
      Iijima K, Sako M, Tuchida N, Ohashi Y.
    • Organizer
      American Society of Nephrology, 2012 Kidney Week
    • Place of Presentation
      San Diego
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] 小児頻回再発型ネフローゼ症候群に対するC2投与量調節法の他施設ランダム化比較(JSKDC03)2012

    • Author(s)
      佐古まゆみ,飯島一誠,斉藤真梨,大橋靖雄,吉川徳茂
    • Organizer
      第55回日本腎臓学会学術総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Genetical and Clinical Aspects of X-Linked Alport Syndrome in Males with Positive Staining of the alpha5(IV) Chain2012

    • Author(s)
      Hashimura Y, Nozu K, Kaito H, Ohtsubo H, Hashimoto F, Ishimori S, Ninchoji T, Morisada N, Nakanishi K, Yoshikawa N, Iijima K
    • Organizer
      45th Annual Meeting of the American Society of Nephrology
    • Place of Presentation
      San Diego, USA
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] 日本人先天性ネフローゼ症候群における原因遺伝子検索2012

    • Author(s)
      向山弘展,中西浩一,戸川寛子,浜 武継,島 友子,飯島一誠,吉川徳茂
    • Organizer
      第55回日本腎臓学会学術総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Histological Predictors of Treatment Efficacy in Severe Childhood IgA Nephropathy (IgAN): Validation of the Oxford Classification of IgAN (Ox C)2012

    • Author(s)
      Shima Y, Nakanishi K, Hama T, Mukaiyama H, Togawa H, Ishimori S, Kaito H, Tanaka R, Iijima K, Yoshikawa N.
    • Organizer
      American Society of Nephrology, 2012 Kidney Week
    • Place of Presentation
      San Diego
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Mutation analysis in Japanese patients with congenital and infantile nephrotic syndrome.2012

    • Author(s)
      Mukaiyama H, Nakanishi K, Hama T, Togawa H, Shima Y, Iijima K, Yoshikawa N.
    • Organizer
      American Society of Nephrology, 2012 Kidney Week
    • Place of Presentation
      San Diego
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Nutcracker症候群を合併した軽症IgA腎症の1例2011

    • Author(s)
      石森真吾、大坪裕美、橋本総子、橋村裕也、貝藤裕史、森貞直哉、飯島一誠、松尾雅文
    • Organizer
      第24回近畿小児科学会
    • Place of Presentation
      神戸国際会議場(兵庫県)
    • Year and Date
      2011-03-12
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] "Alport-like"glomerular basement membrane changes in a Japanese girl with renal-coloboma syndrome due to PAX2 mutation.2011

    • Author(s)
      Otsubo H, Hashimoto S, Ishimori S, Hashimura Y, Fu XJ, Kaito H, Morisada N, Nagatani K, Iijima K, Matsuo M.
    • Organizer
      The 11th Asian Congress of Pediatric Nephrology
    • Place of Presentation
      Fukuoka
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Investigation of molecular background for patients with exercise-idcuced acute renal failure.2011

    • Author(s)
      Kaito H, Nozu K,Nakanishi K, Hashimura Y,Shima Y,Ninchoji T,Yoshikawa N,Iijima K,Matsuo M.
    • Organizer
      ERA-EDTA Congress
    • Place of Presentation
      Praha
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Clinical characteristics of silent lupus nephritis in children: a single center experience.2011

    • Author(s)
      Ishimori S, Otsubo H, Hashimoto F, Hashimura Y, Kaito H, Morisada N, Yoshikawa N,
    • Organizer
      The 11th Asian Congress of Pediatric Nephrology
    • Place of Presentation
      Fukuoka
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Cyclosporine C2 monitoring for frequent-relapsing nephrotic syndrome in children: A multicenter randomized controlled trial2011

    • Author(s)
      Iijima K, Sako Nakamura M, Saito M, Ohashi Y, Yoshikawa N
    • Organizer
      American Society of Nephrology Kidney Week 2012
    • Place of Presentation
      Philadelphia
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Alport syndrome associated with hemophilia A-molecular mechanism of phenotypic divergence between siblings.2011

    • Author(s)
      Hashimura Y, Nozu K, Otsubo H, Hashimoto S, Ishimori S, Morisada N, Kaito H,
    • Organizer
      Pediatric Academic Societies' 2011Annual Meeting
    • Place of Presentation
      Denver
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] 小児難治性ネフローゼ症候群の新たな治療戦略2011

    • Author(s)
      飯島一誠
    • Organizer
      第41回日本腎臓学会西部学術大会(招待講演)
    • Place of Presentation
      徳島
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Clinical distinction between genetically-proven gitelman's and pseudo-gitelman's syndrome2011

    • Author(s)
      Ninchoji T,Kaito H, Nozu K,Hashimura Y,Nakanishi K, Yoshikawa N,Iijima K,Matsuo M
    • Organizer
      ERA-EDTA Congress
    • Place of Presentation
      Praha
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Genetic Backgrounds in Patients with Glomerulopathy with Fibronectin2011

    • Author(s)
      Ohtsubo H,Hashimoto F,Ishimori S,Ninchoji T,Fu XueJun,Hashimura Y,Kaito H,Morisada N,Uesugi N,Iijima K.
    • Organizer
      American Society of Nephrology Kidney Week 2012
    • Place of Presentation
      Philadelphia
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Deep intronic mutations in COL4A5 causes X-linked Alport syndrome.2011

    • Author(s)
      Hashimoto F, Nozu K, Otsubo H, Ishimori S, Hashimura Y, Kaito H, Nakanishi K,
    • Organizer
      The 11th Asian Congress of Pediatric Nephrology
    • Place of Presentation
      Fukuoka
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Recurrent exercise-induced acute renal failure and PRES with severe renal hypouricemia by2011

    • Author(s)
      Shima Y, Nozu K, Togawa H, Kaito H, Iijima K, Matsuo M, Nakanishi K, Yoshikawa N.
    • Organizer
      Pediatric Academic Societies' 2011Annual Meeting
    • Place of Presentation
      Denver
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] Rituximab for refractory nephrotic syndrome2011

    • Author(s)
      Iijima K
    • Organizer
      The 11th Asian Congress of Pediatric Nephrology(招待講演)
    • Place of Presentation
      Fukuoka
    • Data Source
      KAKENHI-PROJECT-23591192
  • [Presentation] 遺伝子解析で確定診断しえたGitelman症候群31例の臨床的検討2010

    • Author(s)
      貝藤裕史、野津寛大、橋村裕也、岡政史、忍頂寺毅史、飯島一誠、松尾雅文
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Clinical Characteristics of Genetically-Proven Gitelman's Syndrome2010

    • Author(s)
      Kaito H,Nozu N,Hashimura Y,Oka M,Ninchoji T,Nakanishi K,Yoshikawa N,Iijima K,Matsuo M
    • Organizer
      the 15th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      New York Hilton(アメリカ)
    • Year and Date
      2010-08-29
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 3歳健診から血尿と蛋白尿が持続し,Alport症候群の孤発例と考えられた女児例2010

    • Author(s)
      海野杏奈、沢登恵美、松下香子、東田耕輔、杉田完爾、野津寛大、Krol Rafal P、飯島一誠
    • Organizer
      第113回日本小児科学会学術集会
    • Place of Presentation
      いわて県民情報交流センター(岩手県)
    • Year and Date
      2010-04-25
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] ステロイド依存性ネフローゼ症候群に対するリツキシマブ単回投与後のミコフェノール酸モフェチルによる維持療法の有効性2010

    • Author(s)
      伊藤秀一、堤晶子、野田俊輔、宇田川智宏、小椋雅夫、佐古まゆみ、亀井宏一、飯島一誠
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] シンポジウム1「腎炎,ネフローゼの免疫抑制療法Update2010(ループス腎炎を含む)」小児難治性ネフローゼ症候群に対するリツキシマブ医師ま導治験2010

    • Author(s)
      飯島一誠
    • Organizer
      第53回日本腎臓学会学術総会
    • Place of Presentation
      神戸国際会議場(兵庫県)(招待講演)
    • Year and Date
      2010-06-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 小児の膜性腎症におけるIgGサブクラスの検討2010

    • Author(s)
      亀井宏一、松岡健太郎、野田俊輔、宇田川智宏、堤晶子、小椋雅夫、中川温子、三浦健一郎、五十嵐隆、藤永周一郎、戸川寛子、中西浩一、吉川徳茂、飯島一誠、伊藤秀一
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] X染色体連鎖型Alport症候群と血友病Aを合併した一男児例-同胞男児間における表現型の差異についての分子遺伝学的検討-2010

    • Author(s)
      橋村裕也、野津寛大、岡政史、忍頂寺毅史、貝藤裕史、飯島一誠、松尾雅文
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Epithelial-to-Mesenchymal Transition(EMT)in cpk Mouse, a Model of ARPKD2010

    • Author(s)
      Togawa H, Nakanishi K, Mukaiyama H, Hama T, Shima Y, Miyajima M, Nozu K, Takahashi H, Nagao S,Iijima K, Yoshikawa N
    • Organizer
      Renal Week 2010
    • Place of Presentation
      Colorado Convention Center(アメリカ)
    • Year and Date
      2010-11-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Long-Term Morbidity in Children with Frequently Relapsing Nephrotic Syndrome after a Randomized Controlled Trial with Cyclosporine2010

    • Author(s)
      Ishikura K, Yoshikawa N, Sasaki S, Iijima K, Nakanishi K, Ito S, Matsuyama T, Yata N, Ando T, Honda M
    • Organizer
      Renal Week 2010
    • Place of Presentation
      Colorado Convention Center(アメリカ)
    • Year and Date
      2010-11-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 伴性優性遺伝の家族性良性血尿の1家系2010

    • Author(s)
      田中幸代、蓮井正史、野津寛大、飯島一誠、杉本圭相、竹村司、金子一成
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 運動後急性腎不全とPRESの合併を反復し、GLUT9遺伝子複合ヘテロ接合体変異を同定しえた腎性低尿酸血症の一例2010

    • Author(s)
      島友子、野津寛大、戸川寛子、貝藤裕史、飯島一誠、松尾雅文、中西浩一、吉川徳茂
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 微小変化・巣状メサンギウム増殖を示す小児IgA腎症における自然寛解率とその予測因子2010

    • Author(s)
      島友子、中西浩一、戸川寛子、野津寛大、田中亮二郎、飯島一誠、吉川徳茂
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 幼少期発症のFibronectin腎症でFN1遺伝子に変異のあった1例2010

    • Author(s)
      川西智子、笠原正登、森潔、横井秀基、桑原孝成、城謙輔、上杉憲子、長田道夫、野津寛大、飯島一誠、向山政志、中尾一和
    • Organizer
      第40回日本腎臓学会西部学術大会
    • Place of Presentation
      広島国際会議場(広島県)
    • Year and Date
      2010-10-08
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] シンポジウム9「ネフローゼ症候群Up-to-Date」難治性ネフローゼ症候群に対する新規治療法開発の現状2010

    • Author(s)
      飯島一誠
    • Organizer
      第113回日本小児科学会学術集会
    • Place of Presentation
      いわて県民情報交流センター(岩手県)(招待講演)
    • Year and Date
      2010-04-25
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 難治性ネフローゼ症候群に対するリツキシマブ療法の有害事象についての検討2010

    • Author(s)
      亀井宏一、堤晶子、野田俊輔、宇田川智宏、小椋雅夫、佐古まゆみ、飯島一誠、伊藤秀一
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 多嚢胞性異形成腎(MCDK)の兄弟例におけるHNF-1β遺伝子変異2010

    • Author(s)
      蓮井正史、磯崎夕佳、田中幸代、金子一成、野津寛大、飯島一誠
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] COL4A3/COL4A4のヘテロ変異を有する菲薄基底膜症候群のドナーから腎移植を実施した2例2010

    • Author(s)
      梶保祐子、水谷誠、谷口貴実子、上田博章、古山政幸、石塚喜世伸、藤井寛、近本裕子、秋岡祐子、岡政史、野津寛大、飯島一誠、服部元史
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] The Relationship between Arginine Vasopressin Levels and Hyponatremia in Children Receiving Hypotonic or Isotonic Intravenous Fluids Following a Percutaneous Renal Biopsy2010

    • Author(s)
      Michael L.Moritz,Nozu K, Iijima K
    • Organizer
      Renal Week 2010
    • Place of Presentation
      Colorado Convention Center(アメリカ)
    • Year and Date
      2010-11-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 常染色体劣性遺伝を呈したAlport症候群の一例2010

    • Author(s)
      藤本陽子、古野由美、椛島成利、中俣潤一、坂東健一郎、柴田達哉、芹野良太、岡政史、飯島一誠、野津寛大、田村雅仁、尾辻豊
    • Organizer
      第53回日本腎臓学会学術総会
    • Place of Presentation
      神戸国際会議場(兵庫県)
    • Year and Date
      2010-06-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Clinical and Immunohistochemical Analyses of Japanese Families with Genetically-Defined Autosomal-Recessive Alport Syndrome2010

    • Author(s)
      Iijima K, Oka M, Hashimura Y, Otsuka Y, Kaito H, Sado Y, Yan K, Nakanishi K, Yoshikawa N, Nagasako H, Nozu K, Matsuo M
    • Organizer
      Renal Week 2010
    • Place of Presentation
      Colorado Convention Center(アメリカ)
    • Year and Date
      2010-11-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 常染色体劣性多発性嚢胞腎(ARPKD)モデルcpkマウスの尿細管上皮細胞における上皮間葉移行(EMT)2010

    • Author(s)
      戸川寛子、中西浩一、島友子、佐古まゆみ、向山弘展、宮嶋正康、野津寛大、吉原大輔、長尾枝澄香、飯島一誠、吉川徳茂
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Natural Remission Rate and Prognostic Factors in Childhood IgANephropathy with Minimal Change or Focal Mesangial Proliferation2010

    • Author(s)
      Shima Y,Nakanishi K,Togawa H,Nozu N,Tanaka T,Iijima K,Yoshikawa N
    • Organizer
      the 15th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      New York Hilton(アメリカ)
    • Year and Date
      2010-08-29
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 日本人小児の血清クレアチニン基準値2010

    • Author(s)
      上村治、本田雅敬、松山健、秋岡祐子、粟津緑、飯島一誠、池住洋平、石倉健司、伊藤秀一、北山博嗣、佐古まゆみ、関根孝司、永井琢人、幡谷浩史、藤田直也、矢田菜穂子、山田拓司
    • Organizer
      第53回日本腎臓学会学術総会
    • Place of Presentation
      神戸国際会議場(兵庫県)
    • Year and Date
      2010-06-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 日本人小児(1~12歳)のGFR推算式2010

    • Author(s)
      永井琢人、上村治、本田雅敬、松山健、秋岡祐子、粟津緑、飯島一誠、池住洋平、石倉健司、伊藤秀一、北山博嗣、佐古まゆみ、関根孝司、幡谷浩史、藤田直也、矢田菜穂子
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Clinical and Immunohistochemical Analyses of Japanese Families with Genetically-Defined Autosomal-Recessive Alport Syndrome.2010

    • Author(s)
      Iijima K, Oka M, Hashimura Y, Ohtsuka Y, Kaito H, Sado Y, Yan K, Nakanishi K, Yoshikawa N, Nagasako H, Nozu K, Matsuo M.
    • Organizer
      American Society of Nephrology 2010 Annual Meeting
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] National Survey of Rituximab Treatment for Childhood Idiopathic Nephrotic Syndrome2010

    • Author(s)
      Ito S, Kamei K, Ogura M, Udagawa T, Fujinaga S, Iijima K
    • Organizer
      the 15th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      New York Hilton(アメリカ)
    • Year and Date
      2010-08-29
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 特別講演小児難治性ネフローゼ症候群に対するリツキシマブ医師主導治験2010

    • Author(s)
      飯島一誠
    • Organizer
      第3回石川県小児State of the Art Meeting
    • Place of Presentation
      金沢ニューグランドホテル(石川県)(招待講演)
    • Year and Date
      2010-10-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] シンポジウム1『CAKUTに対する治療戦略』CAKUTと遺伝子変異2010

    • Author(s)
      飯島一誠
    • Organizer
      第32回日本小児腎不全学会学術集会
    • Place of Presentation
      定山渓万世閣ホテルミリオーネ(北海道)(招待講演)
    • Year and Date
      2010-09-30
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 平滑筋腫合併アルポート症候群(DL-AS)の遺伝学的検討2010

    • Author(s)
      岡政史、野津寛大、森貞直哉、平野大志、藤永周一郎、忍頂寺毅史、橋村裕也、貝藤裕史、飯島一誠、松尾雅文
    • Organizer
      第53回日本腎臓学会学術総会
    • Place of Presentation
      神戸国際会議場(兵庫県)
    • Year and Date
      2010-06-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 日本人小児の血清シスタチンC基準値2010

    • Author(s)
      矢田菜穂子、上村治、本田雅敬、秋岡祐子、粟津緑、飯島一誠、池住洋平、石倉健司、伊藤秀一、北山博嗣、佐古まゆみ、関根孝司、永井琢人、幡谷浩史、藤田直也、松山健、山田拓司
    • Organizer
      第53回日本腎臓学会学術総会
    • Place of Presentation
      神戸国際会議場(兵庫県)
    • Year and Date
      2010-06-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] シクロスポリンにてネフローゼ症候群と食物アレルギー性腸炎の寛解維持が可能となったIPEX症候群の一例2010

    • Author(s)
      野田俊輔、亀井宏一、堤晶子、宇田川智宏、小椋雅夫、伊藤秀一、松岡健太郎、金兼弘和、野津寛大、飯島一誠
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Prognostic Factors in Childhood IgA Nephropathy with Focal Mesangial Proliferation Treated with Angiotensin Converting Enzyme Inhibitors2010

    • Author(s)
      Shima Y, Nakanishi K, Togawa H, Mukaiyama H, Hama T, Nozu K, Tanaka R, Iijima K, Yoshikawa N
    • Organizer
      Renal Week 2010
    • Place of Presentation
      Colorado Convention Center(アメリカ)
    • Year and Date
      2010-11-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 日本人小児の血清クレアチニン基準値2010

    • Author(s)
      上村治、本田雅敬、松山健、秋岡祐子、粟津緑、飯島一誠、池住洋平、石倉健司、伊藤秀一、北山博嗣、佐古まゆみ、関根孝司、永井琢人、幡谷浩史、藤田直也、矢田菜穂子
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 常染色体性Alport症候群の臨床および分子生物学的検討2010

    • Author(s)
      岡政史、野津寛大、忍頂寺毅史、橋村裕也、貝藤裕史、飯島一誠、松尾雅文
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] シンポジウム「小児ネフローゼ症候群治療のセイフティネット」新たな治療への展望-難治例に対するリツキシマブ-2010

    • Author(s)
      飯島一誠
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)(招待講演)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] X染色体連鎖型Alport症候群の臨床的検討2010

    • Author(s)
      橋村裕也、野津寛大、岡政史、忍頂寺毅史、貝藤裕史、飯島一誠、中西浩一、吉川徳茂、松尾雅文
    • Organizer
      第53回日本腎臓学会学術総会
    • Place of Presentation
      神戸国際会議場(兵庫県)
    • Year and Date
      2010-06-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 「CAKUTに対する治療戦略」CAKUTと遺伝子変異2010

    • Author(s)
      飯島一誠, 野津寛大, 中山真紀子
    • Organizer
      第32回日本小児腎不全学会学術集会
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] レシピエント選定基準改定後に経験した小児献腎移植の5例2010

    • Author(s)
      忍頂寺毅史、橋村裕也、貝藤裕史、野津寛大、飯島一誠、松尾雅文
    • Organizer
      第113回日本小児科学会学術集会
    • Place of Presentation
      いわて県民情報交流センター(岩手県)
    • Year and Date
      2010-04-25
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] LINE-1レトロトランスポゾンの置換によるEYA1遺伝子変異をともなったbranchio-oto-renal症候群の1女児例2010

    • Author(s)
      森貞直哉、野津寛大、Nanna Dahl Rendtorff、森下高弘、宮川隆之、松元透、LisbethTrahebjaerg、飯島一誠、松尾雅文、楠原浩一
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] ヒトARPKDと相同遺伝子変異を有するPCK ratにおける上皮間葉移行2010

    • Author(s)
      戸川寛子、中西浩一、島友子、佐古まゆみ、向山弘展、宮嶋正康、野津寛大、吉原大輔、長尾枝澄香、飯島一誠、吉川徳茂
    • Organizer
      第53回日本腎臓学会学術総会
    • Place of Presentation
      神戸国際会議場(兵庫県)
    • Year and Date
      2010-06-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Encrusted Cystitis Caused by MRSA in a Pediatric Renal Transplant Recipient2010

    • Author(s)
      Tanaka R, Teraoka Y, Shimooka T, Hisamatsu E, Takagi S, Sugita Y, Kamei K, Iijima K
    • Organizer
      the 15th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      New York Hilton(アメリカ)
    • Year and Date
      2010-08-29
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 日本人小児(1~12歳)のGFR推算式2010

    • Author(s)
      永井琢人、上村治、本田雅敬、松山健、秋岡祐子、粟津緑、飯島一誠、池住洋平、石倉健司、伊藤秀一、北山博嗣、佐古まゆみ、関根孝司、幡谷浩史、藤国直也、矢田菜穂子、山田拓司
    • Organizer
      第53回日本腎臓学会学術総会
    • Place of Presentation
      神戸国際会議場(兵庫県)
    • Year and Date
      2010-06-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Treatment Strategy and Outcome for Henoch-Schonlein Purpura Nephritis2010

    • Author(s)
      Ninchoj T, Hashimura Y, Kaito H, Nozu N, Kanda, K, Kamioka I, Shima Y, Hamahira K, Nakanishi K, Tanaka R, Iijima K, Yoshikawa N, Matsuo M
    • Organizer
      the 15th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      New York Hilton(アメリカ)
    • Year and Date
      2010-08-29
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 日本人小児の血清シスタチンC基準値2010

    • Author(s)
      矢田菜穂子、上村治、本田雅敬、秋岡祐子、粟津緑、飯島一誠、池住洋平、石倉健司、伊藤秀一、北山博嗣、関根孝司、永井琢人、幡谷浩史、藤田直也、松山健、山田拓司
    • Organizer
      第45回日本小児腎臓病学会学術集会
    • Place of Presentation
      大阪国際会議場(大阪府)
    • Year and Date
      2010-07-02
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Dependency on Immunosuppressants in Children with Steroid-Resistant Nephrotic Syndrome after Cyclosporine and Steroid Therapy2010

    • Author(s)
      Hamasaki Y, Yoshikawa N, Sasaki S, Iijima K, Nakanishi K, Ito S, Matsuyama T, Ishikura K, Kaneko T, Honda M
    • Organizer
      Renal Week 2010
    • Place of Presentation
      Colorado Convention Center(アメリカ)
    • Year and Date
      2010-11-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 常染色体劣性Alport症候群女児例におけるIV型コラーゲンα1~α6鎖染色の検討2010

    • Author(s)
      三浦健一郎、高橋和浩、関根孝司、柳澤敦広、生井良幸、野津寛大、岡政史、飯島一誠、内藤一郎、五十嵐隆
    • Organizer
      第113回日本小児科学会学術集会
    • Place of Presentation
      いわて県民情報交流センター(岩手県)
    • Year and Date
      2010-04-25
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] A Deep Intronic Mutation in the SLC12A3 Gene Leads to Gitelman Syndrome2009

    • Author(s)
      Nozu K, Iijima K, Kaito H, Hashimura Y, Ninchoji T, Nakanishi K, Yoshikawa N, Matsuo M
    • Organizer
      American Society of Nephrology 2009 Annual Meeting
    • Place of Presentation
      San Diego Convention Center(America)
    • Year and Date
      2009-10-30
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Rituximab for Multi-Drug Resistant Nephrotic Syndrome in Children2009

    • Author(s)
      Ito S, Kamei K, Kaito Y, Saka M, Nakayama M, Iijima K
    • Organizer
      American Society of Nephrology 2009 Annual meeting
    • Place of Presentation
      San Diego Convention Center(America)
    • Year and Date
      2009-10-30
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 遺伝性腎疾患における intron 内の変異に伴う病気発症メカニズム解明のための実験系の確立2009

    • Author(s)
      野津寛大, 貝藤裕史, 橋村裕也, 忍頂寺毅史, 飯島一誠, 松尾雅文, 中西浩一, 吉川徳茂
    • Organizer
      第39回日本腎臓学会西部学術大会
    • Place of Presentation
      和歌山県民文化会館(和歌山県)
    • Year and Date
      2009-10-17
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 等張性輸液は手術後の低ナトリウム(Na)血症を防止する2009

    • Author(s)
      橋村裕也, 神田杏子, 野津寛大, 飯島一誠, 松尾雅文
    • Organizer
      第52回日本腎臓学会学術総会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Year and Date
      2009-06-03
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] IPEX 症候群に微小変化型ネフローゼ症候群を合併した1症例2009

    • Author(s)
      橋村裕也, 野津寛大, 神田杏子, 早川晶, 竹島泰弘, 飯島一誠, 松尾雅文, 中西浩一, 吉川徳茂
    • Organizer
      第44回日本小児腎臓病学会学術集会
    • Place of Presentation
      一橋記念講堂・学術総合センター(東京都)
    • Year and Date
      2009-06-27
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] リツキシマブ療法を施行したステロイド抵抗性ネフローゼの臨床的検討2009

    • Author(s)
      亀井宏一, 伊藤秀一, 貝藤裕史, 佐古まゆみ, 中山真紀子, 大塚泰史, 松村英樹, 服部元史, 飯島一誠
    • Organizer
      第52回日本腎臓学会学術総会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Year and Date
      2009-06-05
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] リツキシマブの投与でステロイド感受性が改善した Collapsing FSGS の1例2009

    • Author(s)
      貝藤裕史, 亀井宏一, 小椋雅夫, 菊池絵梨子, 松岡健太郎, 飯島一誠, 伊藤秀一
    • Organizer
      第44回日本小児腎臓病学会学術集会
    • Place of Presentation
      一橋記念講堂・学術総合センター(東京都)
    • Year and Date
      2009-06-26
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] シンポジウム1「ネフローゼ症候群研究の新たな展開」小児ネフローゼ症候群における治療開発研究の進歩(リツキシマブ医師主導治験も含めて)2009

    • Author(s)
      飯島一誠
    • Organizer
      第52回日本腎臓学会学術総会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Year and Date
      2009-06-03
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] ワークショップ「小児と成人の腎疾患」小児ネフローゼ症候群の治療法2009

    • Author(s)
      飯島一誠
    • Organizer
      第39回日本腎臓学会西部学術大会
    • Place of Presentation
      和歌山県民文化会館(和歌山県)
    • Year and Date
      2009-10-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 小児CKD全国実態調査2009

    • Author(s)
      矢田菜穂子, 上村治, 本田雅敬, 秋岡祐子, 粟津緑, 飯島一誠, 池住洋平, 石倉健司, 伊藤秀一, 北山博嗣, 関根孝司, 永井琢人, 幡谷浩史, 藤田直也, 松山健, 大橋靖雄, 日本小児腎臓病学会小児CKD対策小委員会
    • Organizer
      第44回日本小児腎臓病学会学術集会
    • Place of Presentation
      一橋記念講堂・学術総合センター(東京都)
    • Year and Date
      2009-06-26
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] X染色体連鎖型アルポート症候群(XLAS)の分子遺伝学的検討2009

    • Author(s)
      野津寛大, 貝藤裕史, 神田杏子, 橋村裕也, 飯島一誠, 松尾雅文, 中西浩一, 吉川徳茂
    • Organizer
      第52回日本腎臓学会学術総会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Year and Date
      2009-06-05
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] リツキシマブ投与3ヵ月後に無顆粒球症を呈したステロイド依存性頻回再発型ネフローゼ症候群の7歳男児例2009

    • Author(s)
      平本龍吾, 松本真輔, 江口広宜, 小森功夫, 柴田佐和子, 亀井宏一, 飯島一誠
    • Organizer
      第44回日本小児腎臓病学会学術集会
    • Place of Presentation
      一橋記念講堂・学術総合センター(東京都)
    • Year and Date
      2009-06-27
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 小児CKD全国実態調査2009

    • Author(s)
      矢田菜穂子, 上村治, 本田雅敬, 秋岡祐子, 粟津緑, 飯島一誠, 池住洋平, 石倉健司, 伊藤秀一, 北山博嗣, 佐古まゆみ, 関根孝司, 永井琢人, 幡谷浩史, 藤田直也, 松山健, 山田拓司, 大橋靖雄, 日本小児腎臓病学会小児CKD対策小委員会
    • Organizer
      第52回日本腎臓学会学術総会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Year and Date
      2009-06-03
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Snail1 Is Involved in Epithelial-to-Mesenchymal Transition(EMT)in Cyst-Lining Epithelial Cells in PCK Rat2009

    • Author(s)
      Togawa H, Nakanishi K, Shima Y, Sako M, Miyajima M, Nozu K, Iijima K, Yoshihara D, Nagao S, Yoshikawa N
    • Organizer
      American Socrety of Nephrology 2009 Annual Meeting
    • Place of Presentation
      San Diego Convention Center(America)
    • Year and Date
      2009-10-29
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Investigation of Molecular Background for Patients with Exercise-Induced Acute Renal Failure2009

    • Author(s)
      Kaito H, Nozu K, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M
    • Organizer
      American Society of Nephrology 2009 Annual Meeting
    • Place of Presentation
      San Diego Convention Center(America)
    • Year and Date
      2009-10-31
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 重症小児IgA腎症における治療反応性規定因子2009

    • Author(s)
      島友子, 中西浩一, 戸川寛子, 尾鼻美奈, 野津寛大, 飯島一誠, 田中亮二郎, 佐々木聡, 吉川彼茂
    • Organizer
      第44回日本小児腎臓病学会学術集会
    • Place of Presentation
      一橋記念講堂・学術総合センター(東京都)
    • Year and Date
      2009-06-27
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 教育講演「小児ネフローゼ症候群」2009

    • Author(s)
      飯島一誠
    • Organizer
      第39回日本腎臓学会東部学術大会
    • Place of Presentation
      グランドプリンスホテル新高輪(東京都)
    • Year and Date
      2009-10-03
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] リツキシマブ療法を施行したステロイド抵抗性ネフローゼの臨床的検討2009

    • Author(s)
      亀井宏一, 伊藤秀一, 貝藤裕史, 佐古まゆみ, 中山真紀子, 大塚泰史, 松村英樹, 服部元史, 飯島一誠
    • Organizer
      第44回日本小児腎臓病学会学術集会
    • Place of Presentation
      一橋記念講堂・学術総合センター(東京都)
    • Year and Date
      2009-06-27
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 腎不全に至ったステロイド感受性微小変化型ネフローゼ症候群の1例2009

    • Author(s)
      橋村裕也, 忍頂寺毅史, 貝藤裕史, 野津寛大, 飯島一誠, 中西浩一, 吉川徳茂, 松尾雅文
    • Organizer
      第39回日本腎臓学会西部学術大会
    • Place of Presentation
      和歌山県民文化会館(和歌山県)
    • Year and Date
      2009-10-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] A Deep Intronic Mutation in the SLC12A3 Gene leads to Gitelman Syndrome.2009

    • Author(s)
      Nozu K, Iijima K, Kaito H, Hashimura Y, Ninchoji T, Nakanishi K, Yoshikawa N, Matsuo M.
    • Organizer
      American Society of Nephrology 2009 Annual Meeting
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 遺伝性腎疾患における intron 内の変異に伴う病気発症メカニズム解明のための in vivo および in vitro の実験系の確立2009

    • Author(s)
      野津寛大, 野津圭美, 齋木加代子, 西田篤丈, 貝藤裕史, 神田杏子, 橋村裕也, 中西浩一, 吉川徳茂, 河井和夫, 竹島泰弘, 飯島一誠, 松尾雅文
    • Organizer
      第44回日本小児腎臓病学会学術集会
    • Place of Presentation
      一橋記念講堂・学術総合センター(東京都)
    • Year and Date
      2009-06-27
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 小児ネフローゼ症候群患者におけるリツキシマブ血中濃度と投与後再発についての検討2009

    • Author(s)
      貝藤裕史, 亀井宏一, 菊池絵梨子, 小椋雅夫, 佐古まゆみ, 野津寛大, 藤永秀一郎, 飯島一誠, 伊藤秀一
    • Organizer
      第44回日本小児腎臓病学会学術集会
    • Place of Presentation
      一橋記念講堂・学術総合センター(東京都)
    • Year and Date
      2009-06-26
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 運動後急性腎不全とPRES(Posterior reversible encephalopathy syndrome)の合併を反復した腎性低尿酸血症の1例2009

    • Author(s)
      島友子, 中西浩一, 戸川寛子, 野津寛大, 飯島一誠, 吉川徳茂
    • Organizer
      第39回日本腎臓学会西部学術大会
    • Place of Presentation
      和歌山県民文化会館(和歌山県)
    • Year and Date
      2009-10-16
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] NR3C2遺伝子変異に伴いmRNAに splicing 異常を認めたにも関わらず軽症であった偽性低アルドステロン症1型の親子例2009

    • Author(s)
      神田杏子, 野津寛大, 橋村裕也, 三輪明弘, 森岡一朗, 横山直樹, 飯島一誠, 松尾雅文
    • Organizer
      第44回日本小児腎臓病学会学術集会
    • Place of Presentation
      一橋記念講堂・学術総合センター(東京都)
    • Year and Date
      2009-06-27
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] ヒトARPKD相同遺伝子ラットモデルにおける尿細管部位特異的嚢胞形成2009

    • Author(s)
      戸川寛子, 中西浩一, 島友子, 佐古まゆみ, 宮嶋正康, 野津寛大, 飯島一越, 吉原大輔, 長尾枝澄香, 吉川徳茂
    • Organizer
      第52回日本腎臓学会学術総会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Year and Date
      2009-06-04
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] COL4A5遺伝子に9塩基の欠失を有し GBMに4型コラーゲンα5鎖の正常の発現を認めたX染色体連鎖型アルポート症候群男児例2009

    • Author(s)
      沢登恵美, 海野杏奈, 金井宏明, 松下香子, 杉田完爾, 東田耕輔, 野津寛大, Rafal P Krol, 飯島一誠
    • Organizer
      第44回日本小児腎臓病学会学術集会
    • Place of Presentation
      一橋記念講堂・学術総合センター(東京都)
    • Year and Date
      2009-06-27
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] X染色体連鎖型アルポート症候群の分子遺伝学的検討2009

    • Author(s)
      野津寛大, Krol Rafal, 神田杏子, 橋村裕也, 中西浩一, 吉川徳茂, 飯島一誠, 松尾雅文
    • Organizer
      第112回日本小児科学会学術集会
    • Place of Presentation
      奈良県立文化会館(奈良県)
    • Year and Date
      2009-04-17
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] X染色体連鎖型アルポート症候群の男性患者における糸球体基底膜4型コラーゲンα5鎖陽性例の検討2009

    • Author(s)
      Krol R, Nozu K, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M
    • Organizer
      第44回日本小児腎臓病学会学術集会
    • Place of Presentation
      一橋記念講堂・学術総合センター(東京都)
    • Year and Date
      2009-06-26
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] ARPKD 相同遺伝子ラットモデルの尿細管上皮細胞における上皮間葉移行(EMT)2009

    • Author(s)
      戸川寛子, 中酉浩一, 島友子, 佐古まゆみ, 宮嶋正康, 野津寛大, 飯島一誠, 吉原大輔, 長尾枝澄香, 吉川徳茂
    • Organizer
      第44回日本小児腎臓病学会学術集会
    • Place of Presentation
      一橋記念講堂・学術総合センター(東京都)
    • Year and Date
      2009-06-27
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 免疫抑制療法に効果がなく遺伝子検査より診断したWT1異常症の1例2009

    • Author(s)
      大塚泰史, 岡政史, 酒井菜那, 佐藤忠司, 濱崎雄平, 青木茂久, 久野敏, 飯島一誠, 中山真紀子, 亀井宏一
    • Organizer
      第44回日本小児腎臓病学会学術集会
    • Place of Presentation
      一橋記念講堂・学術総合センター(東京都)
    • Year and Date
      2009-06-27
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 重症小児IgA腎症における治療後腎IgA沈着消失の臨床病理学的意義2009

    • Author(s)
      島友子, 中西浩一, 戸川寛子, 尾鼻美奈, 野津寛大, 飯島一誠, 田中亮二郎, 佐々木聡, 吉川徳茂
    • Organizer
      第52回日本腎臓学会学術総会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Year and Date
      2009-06-03
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Cyclosporine Dependency in Children with Frequently Relapsing Nephrotic Syndrome2009

    • Author(s)
      Ishikura K, Yoshikawa N, Hattori S, Sasaki S, Iijima K, Nakaniahi K, Matauyama T, Yata N, Ando T, Honda M
    • Organizer
      American Society of Nephrology 2009 Annual Meeting
    • Place of Presentation
      San Diego Convention Center(America)
    • Year and Date
      2009-10-30
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Risk factor for proteinuria at the end of combined therapy in severe childhood IgA nephropathy2008

    • Author(s)
      Kamei K, Iijima K, Honda M, Nakanishi K, Yoshikawa N
    • Organizer
      第III回日本小児科学会学術集会
    • Place of Presentation
      東京
    • Year and Date
      2008-04-25
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 小児慢性腎不全患者におけるQOL評価.2008

    • Author(s)
      中山真紀子, 柴田玲子, 伊藤雄平, 本田雅敬, 飯島一誠
    • Organizer
      第43回日本小児腎臓病学会学術集会
    • Place of Presentation
      福岡
    • Year and Date
      2008-06-13
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] ネフローゼ症候群の病態解明への挑戦と治療の標準化 頻回再発型及びステロイド抵抗性ネフローゼ症候群の治療戦略2008

    • Author(s)
      飯島一誠
    • Organizer
      第III回日本小児科学会学術集会
    • Place of Presentation
      東京
    • Year and Date
      2008-04-25
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 尿路感染症の外来治療プロトコルの検討.2008

    • Author(s)
      島田姿野, 堀越裕歩, 道端伸明, 亀井宏一, 飯島一誠, 高山ジョン一郎
    • Organizer
      第III回日本小児科学会学術集会
    • Place of Presentation
      東京
    • Year and Date
      2008-04-27
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Cyclosporine Treatment for Frequent-relapsing Nephrotic Syndrome.2008

    • Author(s)
      Iijima K
    • Organizer
      10th Asian Congress of Pediatric Nephrology 2008
    • Place of Presentation
      Bangkok, Thialand
    • Year and Date
      2008-08-30
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Disappearance of Glomerular IgA Deposits in Severe Childhood IgA Nephropathy after 2-yr Combination/Prednisolone Therapy.2008

    • Author(s)
      Shima Y, Nakanishi K, Togawa H, Obana M, Nozu K, Tanaka R, Sasaki s, Iijima K, Yoshikawa N.
    • Organizer
      American Society of Nephrology 2008 Annual Meeting
    • Place of Presentation
      Philadelphia, USA
    • Year and Date
      2008-11-07
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 肺炎球菌感染による溶血性尿毒症症候群をきたした乳児例.2008

    • Author(s)
      鶴見晴子, 伊藤純子, 元田玲奈, 佳久哲宜, 大関由紀子, 寺町昌史, 亀井宏一, 飯島一誠, 横谷進.
    • Organizer
      第43回日本小児腎臓病学会学術集会
    • Place of Presentation
      福岡
    • Year and Date
      2008-06-13
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Epithelial-to-Mesenchymal Transition in Cyst-Lining Epithelial Cells in PCK Rat、2008

    • Author(s)
      Togawa H, Nakanishi K, Obana M, Shima Y, Miyajima M, Nozu K, Iijima K, Nishi K, Nagao S, Takahashi H, Yoshikawa N.
    • Organizer
      American Society of Nephrology 2008 Annual Meeting
    • Place of Presentation
      Philadelphia, USA
    • Year and Date
      2008-11-07
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 巨大血小板を伴う遺伝性腎症(Epstein症候群)の2症例 : 遺伝学的背景と臨床経過.2008

    • Author(s)
      関根孝司, 井田孔明, 稲冨淳, 堀尾恵三, 三浦健一郎, 國島伸治, 飯島一誠, 亀井宏二五十嵐隆.
    • Organizer
      第43回日本小児腎臓病学会学術集会
    • Place of Presentation
      福岡
    • Year and Date
      2008-06-14
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] The First Case of Minimal Change Nephrotic Syndrome Associated with Immunodysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome2008

    • Author(s)
      Hashimura Y, Nozu K, Kanda K, Takeshima Y, Hayakawa A, Iijima K, Matsuo M
    • Organizer
      American Society of Nephrology 2008 Annual Meeting
    • Place of Presentation
      Philadelphia, USA
    • Year and Date
      2008-11-06
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 小児ネフローゼ症候群におけるDystroglycan染色性とステロイド反応性の検討.2008

    • Author(s)
      松岡健太郎, 倉持茂, 倉山英昭, 今澤俊之, 飯島一誠, 城謙輔
    • Organizer
      第51回日本腎臓学会学術総会
    • Place of Presentation
      福岡
    • Year and Date
      2008-05-31
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] TCF2 Mutation in Patients with Congenital Anomalies of the Kidney and Urinary Tract (CAKUT).2008

    • Author(s)
      Nakayama M, Nozu K, Goto Y, Kamei K, Sato H, Emi M, Iijima K.
    • Organizer
      American Society of Nephrology 2008 Annual Meeting
    • Place of Presentation
      Philadelphia, USA
    • Year and Date
      2008-11-07
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 採尿を必要としないイヌリンクリアランス(血漿法)の試み2008

    • Author(s)
      亀井宏一, 笠原克明, 白川利彦, 寺町昌史, 中山真紀子, 鈴木輝明, 飯島一誠
    • Organizer
      第51回日本腎臓学会学術総会
    • Place of Presentation
      福岡
    • Year and Date
      2008-05-31
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 常染色体劣性多発性嚢胞腎で生体肝腎同時移植を行った4歳女児例.2008

    • Author(s)
      亀井宏一, 寺町昌史, 笠原克明, 白川利彦, 中山真紀子, 鈴木輝明, 土田聡子, 石倉健司, 飯島一誠, 松井陽
    • Organizer
      第III回日本小児科学会学術集会
    • Place of Presentation
      東京
    • Year and Date
      2008-04-25
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] ステロイドは血清シスタチンCを増加させる.2008

    • Author(s)
      亀井宏一, 笠原克明, 白川利彦, 寺町昌史, 中山真紀子, 鈴木輝明, 飯島一誠
    • Organizer
      第43回日本小児腎臓病学会学術集会
    • Place of Presentation
      福岡
    • Year and Date
      2008-06-14
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Somatic Mosaicism for a Mutation of the COL4A5 Gene in Three Sporadic X-Linked Alport Syndrome Cases.2008

    • Author(s)
      Nozu K, Krol PR, Nakanishi K, Yoshikawa N, Kaito H, Kanda K, Hashimura Y, Iijima K, Matsuo M.
    • Organizer
      American Society of Nephrology 2008 Annual Meeting
    • Place of Presentation
      Philadelphia, USA
    • Year and Date
      2008-11-08
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] The First Case of Minimal Change Nephrotic Syndrome Associated with Immunodysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome.2008

    • Author(s)
      Hashimura Y, Nozu K, Kanda K, Takeshima Y, Hayakawa A, Iijima K, Matsuo M.
    • Organizer
      American Society of Nephrology 2008 Annual Meeting
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 重症型IgA腎症におけるカクテル療法終了時の蛋白尿残存に寄与する因子の検討.2008

    • Author(s)
      亀井宏一, 飯島一誠, 本田雅敬, 中西浩一, 吉川徳茂.
    • Organizer
      第43回日本小児腎臓病学会学術集会
    • Place of Presentation
      福岡
    • Year and Date
      2008-06-14
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] TCF2 Mutation in Patients with Congenital Anomalies of the Kidney and Urinary Tract (CAKUT).2008

    • Author(s)
      Nakayama M, Nozu K, Goto Y, Kamei K, Sato H, Emi M, Iijima K
    • Organizer
      American Society of Nephrology 2008 Annual Meeting
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Elevated AVP Levels and Hyponatremia Following Percutaneous Renal Biopsies in Children.2008

    • Author(s)
      Moritz ML, Iiiima K, Matsuo M, Kanda K, Nozu K.
    • Organizer
      American Society of Nephrology 2008 Annual Meeting
    • Place of Presentation
      Philadelphia, USA
    • Year and Date
      2008-11-07
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 運動後急性腎不全8症例におけるURATl遺伝子解析の検討.2008

    • Author(s)
      貝藤裕史, 野津寛大, 飯島一誠, 中西浩一, 太田和秀, 藤枝幹也, 由良和夫, 亀井宏一, 横山忠史, 石原正行, 島友子, 神田杏子, 吉川徳茂, 松尾雅文
    • Organizer
      第43回日本小児腎臓病学会学術集会
    • Place of Presentation
      福岡
    • Year and Date
      2008-06-13
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 当院における小児劇症肝不全10症例に対する人工肝補助の経験.2008

    • Author(s)
      白川利彦, 亀井宏一, 笠原群生, 清水直樹, 中川聡, 肥沼幸, 新井勝大, 寺町昌史, 笠原克明, 中山真紀子, 鈴木輝明, 飯島一誠
    • Organizer
      第43回日本小児腎臓病学会学術集会
    • Place of Presentation
      福岡
    • Year and Date
      2008-06-13
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 先天性腎尿路奇形におけるTCF2遺伝子異常2008

    • Author(s)
      中山真紀子, 後藤由紀, 亀井宏一, 野津寛大, 飯島一誠.
    • Organizer
      第43回日本小児腎臓病学会学術集会
    • Place of Presentation
      福岡
    • Year and Date
      2008-06-14
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] IgA沈着が消失した重症型小児IgA腎症26例の検討2008

    • Author(s)
      島友子, 中西浩一, 戸川寛子, 尾鼻美奈, 野津寛大, 田中亮二郎, 佐々木聡, 飯島一誠, 吉川徳茂.
    • Organizer
      第43回日本小児腎臓病学会学術集会
    • Place of Presentation
      福岡
    • Year and Date
      2008-06-14
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] X染色体連鎖型アルポート症候群の分子遺伝学的検討.2008

    • Author(s)
      野津寛大, KrolRafal, 貝藤裕史, 神田杏子, 橋村裕也, 松尾雅文, 中西浩一, 吉川徳茂, 飯島一誠.
    • Organizer
      第43回日本小児腎臓病学会学術集会
    • Place of Presentation
      福岡
    • Year and Date
      2008-06-14
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 発端者のCOL4A5遺伝子に体細胞モザイクに変異を有し、軽症の臨床症状を示したAlport症候群の2家系.2008

    • Author(s)
      野津寛大, 貝藤裕史, 神田杏子, 松尾雅文, 島友子, 戸川寛子, 中西浩一, 吉川徳茂, 飯島一誠.
    • Organizer
      第43回日本小児腎臓病学会学術集会
    • Place of Presentation
      福岡
    • Year and Date
      2008-06-14
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 小手術後の一過性血漿抗利尿ホルモン分泌亢進に関する研究.2008

    • Author(s)
      神田杏子, 野津寛大, 貝藤裕史, 松尾雅文, 中西浩一, 吉川徳茂, 飯島一誠
    • Organizer
      第51回日本腎臓学会学術総会
    • Place of Presentation
      福岡
    • Year and Date
      2008-05-31
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] 小児におけるイヌリンクリアランスの試み2008

    • Author(s)
      亀井宏一, 笠原克明, 白川利彦, 寺町昌史, 中山真紀子, 鈴木輝明, 飯島一誠
    • Organizer
      第51回日本腎臓学会学術総会
    • Place of Presentation
      福岡
    • Year and Date
      2008-05-31
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Treatment of Refractory Steroid-Dependent Nephrotic Syndrome with a Single Dose of Rituximab, a Multicenter Prospective Study.2008

    • Author(s)
      Kamei K, Nozu K, Ito S, Fujinaga S, Iijima K.
    • Organizer
      American Society of Nephrology 2008 Annual Meeting
    • Place of Presentation
      Philadelphia, USA
    • Year and Date
      2008-11-07
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] III型Bartter症候群患者における利尿剤負荷試験 Gitelman症候群との類似性の機序に関する研究.2008

    • Author(s)
      神田杏子, 野津寛大, 貝藤裕史, 松尾雅文, 亀井宏一, 飯島一誠, 中西浩一, 吉川徳茂, 関根孝司, 五十嵐隆, 小松博史, 宮下律子.
    • Organizer
      第43回日本小児腎臓病学会学術集会
    • Place of Presentation
      福岡
    • Year and Date
      2008-06-14
    • Data Source
      KAKENHI-PROJECT-20390240
  • [Presentation] Long term prognosis of severe childhood IgA nephropathy after combined therapy2007

    • Author(s)
      Kamei K., Iijima K., Honda M, Nakanishi K., Yoshikawa N
    • Organizer
      The 14th Congress of the International Pediathc Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] for Japanese Study Group of Renal Disease in Children2007

    • Author(s)
      Ishikura K., Ikeda M., Hattori S., Yoshikawa N., Sasaki S., Iijima K., Nakanishi K., Yata N., Honda M.
    • Organizer
      The 14th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Combination therapy with mizoribine for severe childhood IgA nephropathy : A pilot study2007

    • Author(s)
      Nakanishi K., Ishikura K., Hataya H., Ikeda M., Iijima K., Honda M.,Yoshikawa N.
    • Organizer
      The 14th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Genetic Backgrounds in Patients with Exercise-Induced Acute Renal FaiIure2007

    • Author(s)
      Kaito H., Nozu K., Kanda K, Nakanishi K., Yoshiya K., Iijima K., Yoshikawa N., Matsuo M
    • Organizer
      American Society of Nephrology 2007 Annual Meeting
    • Place of Presentation
      San Francisco
    • Year and Date
      2007-11-03
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Transient elevation of plasma antidiuretic hormone level after kidney biopsy associated with iatrogenic hyponatremia or postoperative nausea and vomit2007

    • Author(s)
      Kanda K., Nozu K., Kaito H., Krol R., Nakanishi K., Yoshikawa N., Iijima K., Matsuo M
    • Organizer
      The 14th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Combination therapy with nlizohbine for severe chidhood IgA nephropathy:A pilot study2007

    • Author(s)
      Nakanishi K., Ishikura K., Hataya H., Ikeda M., Iijima K., Honda M., Yoshikawa N.The Japanese Pediathc IgA Nephropathy Treatment Study Group
    • Organizer
      Amehcan Society of Nephrology 2007 Annual Meeting
    • Place of Presentation
      San Francisco
    • Year and Date
      2007-11-03
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Identification of 6 novel mutations in the COL4A5 gene of Japanese Patients with X-linked Alport syndrome2007

    • Author(s)
      Krol R., Nozu K., Kanda K., Kaito H., Nakanishi K, YoshikawaN., Kamei K., Iijima K., Matsuo M
    • Organizer
      The 14th Congress of the International Pediathc Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Combination therapy with mizoribine for severe childhood IgA nephropathy: A pilot study2007

    • Author(s)
      Nakanishi K., Ishikura K., Hataya H., Ikeda M., Iijima K., Honda M., Yoshikawa N. The Japanese Pediatrie IgA Nephropathy Treatment Study Group
    • Organizer
      American Society of Nephrology 2007 Annual Meeting
    • Place of Presentation
      San Francisco
    • Year and Date
      2007-11-03
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] A 2-year, Prospective, Randomized, Multicenter Trial of Moderate-dose Cyclosporine in Children with Frequently Relapsing Nephrotic Syndrome2007

    • Author(s)
      Ishikura K., Ikeda M., Hattori S., Yoshikawa N., Sasaki S., Iijima K., Nakanishi K., Yata N., Honda M., for Japanese Study Group of Renal Disase in Children
    • Organizer
      The 14th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Long term prognosis of severe childhood IgA nephropathy after combined therapy2007

    • Author(s)
      Kamei K., Iijima K., Honda M., Nakanishi K., Yoshikawa N
    • Organizer
      American Society of Nephrology 2007 Annual Meeting
    • Place of Presentation
      San Francisco
    • Year and Date
      2007-11-03
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Long term prognosis of severe childhood IgA nephropathy after combined therapy2007

    • Author(s)
      Kamei K., Iijima K., Honda M., Nakanishi K., Yoshikawa N
    • Organizer
      The 14th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] 「Evidenceとなる臨床研究をおこなうために」厚生労働科学研究小児疾患臨床研究事業「小児腎移植におけるミコフェノール酸モフェチルの有効性・安全性の確認、用法・用量の検計・確立に関する研究(H17-小児-002)」2007

    • Author(s)
      飯島 一誠
    • Organizer
      第42回日本小児腎臓病学会学術集会
    • Place of Presentation
      横浜
    • Year and Date
      2007-06-29
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Clinical Research for Pediatric Renal Transplantation in Japan2007

    • Author(s)
      Iijima K.
    • Organizer
      The 42th Annual Meeting of Japanese Society for Pediatric Nephrology
    • Place of Presentation
      Yokohama
    • Year and Date
      2007-01-29
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Molecular analysis of 5 Japanese Patients with Type III Bartter Syndrome2007

    • Author(s)
      Nozu K., Nakanishi K., Yoshikawa N., Kaito H.Kanda K., KrolR., Satomura K., Shimizu N., Iijima K., Matsuo M
    • Organizer
      The 14th Congress of the International Pediathc Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Rituximab Therapy for Refractory Focal Segmental Glomerulosclerosis2007

    • Author(s)
      Nakayama M., Kamei K., Matsuoka K., Nakagawa A., Iijima K
    • Organizer
      American Society of Nephrology 2007 Annual Meeting
    • Place of Presentation
      San Francisco
    • Year and Date
      2007-11-03
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Molecular analysis of 5Japanese Patients with Type III Bartter Syndrome2007

    • Author(s)
      Nozu K., Nakanishi K, Yoshikawa N., Kaito H Kanda K, Krol R., Satomura K., Shimizu N., Iijima K, Matsuo M.
    • Organizer
      The 14th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Molecular analysis of 5 Japanese Patients with Type III Bartter Syndrome2007

    • Author(s)
      Nozu K., Nakanishi K., Yoshikawa N., Kaito H. Kanda K., Krol R., Satomura K., Shimizu N., Iijima K., Matsuo M
    • Organizer
      The 14th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Combination therapy with mizohbine for severe chidhood IgA nephropathy:Apilot study2007

    • Author(s)
      Nakanishi K., Ishikura K., Hataya H., Ikeda M., Iijima K., Honda M., Yoshikawa N
    • Organizer
      The 14th Congress of the International PediathcNephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Transient elevation of plasma antidiuretic hormone level after kidney biopsy associated with iatrogenic hyponatremia or postoperative nausea and vomit2007

    • Author(s)
      Kanda K., Nozu K., Kaito H., Krol R., Nakanishi K., YoshikawaN., Iijim K., Matsuo M
    • Organizer
      The 14th Congress of the International Pediathc Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Long term prognosis of severe childhood IgA nephropathy after combinedtherapv2007

    • Author(s)
      Kamei K., Iijima K., Honda M., Nakanishi K., Yoshikawa N
    • Organizer
      Amehcan Society of Nephrology 2007 Annual Meeting
    • Place of Presentation
      San Francisco
    • Year and Date
      2007-11-03
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Combination therapy with mizoribine for severe childhood IgA nephropathy: A pilot study2007

    • Author(s)
      Nakanishi K., Ishikura K., Hataya H., Ikeda M., Iijima K., Honda M., Yoshikawa N
    • Organizer
      The 14th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Rituximab therapy for focal segmental glomerulosclerosis2007

    • Author(s)
      Nakayama M., Teramachi M., Kasahara K., Kamei K., Suzuki T., Matsuoka K., Nakagawa A., Iijima K
    • Organizer
      The 14th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Identification of 6 novel mutations in the COL4A5 gene of Japanese Patients with X-linked Alport syndrome2007

    • Author(s)
      Krol R., Nozu K., Kanda K., Kaito H., Nakanishi K., Yoshikawa N., Kamei K., Iijima K., Matsuo M
    • Organizer
      The 14th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Molecular Analysis of Diggenic Inheritance in Type IV Bartter Syndrome Phenotype2007

    • Author(s)
      Nozu K., Kaito H., Nakanishi K., Yoshikawa N., Iijima K., Matsuo M.
    • Organizer
      American Society of Nephrology 2007 Annual Meeting
    • Place of Presentation
      San Francisco
    • Year and Date
      2007-11-03
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] A 2-year, Prospective, Randomized, Multicenter Trial of Moderate-dose Cyclospohne in Chidren with Frequently Relapsing Nephrotic Syndrome2007

    • Author(s)
      Ishikura K., Ikeda M., Hattoh S., Yoshikawa N., Sasaki S., Iijima K., Nakanishi K., Yata N., Honda M., for Japanese Study Group of Renal Disease in Chidren
    • Organizer
      The 14th Congress of the International PediathcNephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Genetic Backgrounds in Patients with Exercise-Induced Acute Renal Failure2007

    • Author(s)
      Kaito H., Nozu K., Kanda K., Nakanishi K., Yoshiya K., Iijima K., Yoshikawa N., Matsuo M
    • Organizer
      American Society of Nephrology 2007 Annual Meeting
    • Place of Presentation
      San Francisco
    • Year and Date
      2007-11-03
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Long term prognosis of severe childhood IgAnephropathy after combined therapy2007

    • Author(s)
      Kamei K . Iijima K., Honda M., Nakanishi K., Yoshikawa N
    • Organizer
      The 14th Congress of the International Pediatric Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Molecular Analysis of Digenic Inheritance in Type IV Bartter Syndrome Phenotype2007

    • Author(s)
      Nozu K., Kaito H., Nakanishi K., Yoshikawa N., Iijima K., Matsuo M
    • Organizer
      American Society of Nephrology 2007 Annual Meeting
    • Place of Presentation
      San Francisco
    • Year and Date
      2007-11-03
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Rituximab therapy for focal segmental glomerulosclerosis2007

    • Author(s)
      Nakayama M., Teramachi M., Kasahara K., Kamei K., Suzuki T., Matsuoka K., Nakagawa A., Iijima K
    • Organizer
      The 14th Congress of the International Pediathc Nephrology Association
    • Place of Presentation
      Budapest
    • Year and Date
      2007-09-02
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Molecular Analysis of Digenic Inhehtance in TYpe IV Bartter Syndrome Phenotype2007

    • Author(s)
      Nozu K., Kaito H., Nakanishi K., Ybshikawa N., Iijima K., Matsuo M
    • Organizer
      American Society of Nephrology 2007 Annual Meeting
    • Place of Presentation
      San Francisco
    • Year and Date
      2007-11-03
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] 「Evidenceとなる臨床研究をおこなうために」厚生労働科学研究小児疾患臨床研究事業「小児腎移植におけるミコフェノール酸モフェチルの有効性・安全性の確認、用法・用量の検討・確立に関する研究(H17-小児-002)」2007

    • Author(s)
      飯島 一誠
    • Organizer
      第42回日本小児腎臓病学会学術集会
    • Place of Presentation
      横浜
    • Year and Date
      2007-06-29
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] The Japanese Pediatric IgA Nephropathy Treatment Study Group. Combination therapy with mizoribine for severe childhood IgA nephropathy : Apilot study2007

    • Author(s)
      Nakanishi K., Ishikura K, Hataya H., Ikeda M., Iijima K., Honda M., Yoshikawa N.
    • Organizer
      American Society of Nephrology 2007 Annual Meeting
    • Place of Presentation
      San Francisco
    • Year and Date
      2007-11-03
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18590920
  • [Presentation] Alport症候群:軽症患者における病理学的および分子生物学的検討

    • Author(s)
      野津寛大
    • Organizer
      第13回日本腎病理協会研究会
    • Place of Presentation
      東京
    • Year and Date
      2015-01-10 – 2015-01-11
    • Invited
    • Data Source
      KAKENHI-PROJECT-25893131
  • [Presentation] Autosomal Dominant Alport Syndrome: Molecular Analysis of the COL4A3/COL4A4 Genes and Clinical Outcome.

    • Author(s)
      Kamiyoshi N, Nozu k, Matsunoshita N, Ohtsubo H, Ninchoji T, Kaito H, Nakanishi N, Yoshikawa N, Iijima K
    • Organizer
      American Society of Nephrology Kidney Week 2014
    • Place of Presentation
      Pennsylvania Convention Center (Philadelphia, USA)
    • Year and Date
      2014-11-11 – 2014-11-16
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] X-linked Alport syndrome patients caused by atypical splicing mutations in COL4A5.

    • Author(s)
      Nozu K, Morisada N, Kaito H, Ninchoji T, Nakanishi K, Yoshikawa N, Iijima K
    • Organizer
      47th Annual Scientific Meeting of the European Society for Pediatric Nephrology
    • Place of Presentation
      Alfandega Congress Center (Porta, Portugal)
    • Year and Date
      2014-09-18 – 2014-09-20
    • Data Source
      KAKENHI-PROJECT-26293203
  • [Presentation] X-linked Alport syndrome patients caused by atypical splicing mutations in COL4A5

    • Author(s)
      Kandai Nozu, Naoya Morisada, Hiroshi Kaito, Takeshi Ninchoji, Koichi Nakanishi, Norishige Yoshikawa, Kazumoto Iijima
    • Organizer
      Annual Meeting of the European Society for Pediatric Nephrology
    • Place of Presentation
      Port
    • Year and Date
      2014-09-18 – 2014-09-20
    • Data Source
      KAKENHI-PROJECT-25893131
  • [Presentation] アルポート症候群-重症軽症を規定する因子に関する再考

    • Author(s)
      野津寛大
    • Organizer
      第49回日本小児腎臓病学会学術集会
    • Place of Presentation
      秋田
    • Year and Date
      2014-06-05 – 2014-06-07
    • Invited
    • Data Source
      KAKENHI-PROJECT-25893131
  • [Presentation] Alport syndrome

    • Author(s)
      Kandai Nozu
    • Organizer
      The 12th Japan-Korea Pediatric Nephrology Seminar
    • Place of Presentation
      Kobe
    • Year and Date
      2014-04-19 – 2014-04-20
    • Invited
    • Data Source
      KAKENHI-PROJECT-25893131
  • 1.  NOZU Kandai (70362796)
    # of Collaborated Projects: 10 results
    # of Collaborated Products: 0 results
  • 2.  SHONO Akemi (10535066)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 25 results
  • 3.  YOSHIKAWA Norishige (10158412)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 18 results
  • 4.  堀之内 智子 (30754593)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 19 results
  • 5.  長野 智那 (60814316)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 13 results
  • 6.  NAGATA Michio (10192238)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 15 results
  • 7.  NAKAYAMA Makioko (80469999)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 23 results
  • 8.  MORISADA Naoya (00389446)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 63 results
  • 9.  TSUKAGUCHI Hiroyasu (60335792)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 14 results
  • 10.  HASHIMURA Yuya (80457077)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 39 results
  • 11.  NAKANISHI Kouichi (50336880)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 27 results
  • 12.  DOI Toshio (60183498)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 13.  KAGAMI Shoji (00224337)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 14.  Takeshi Ninchoji (10568950)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 15.  Yamamura Tomohiko (30770242)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 16.  MINAMIKAWA Shogo (10772634)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 17.  高岡 裕 (20332281)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 18.  人見 祐基 (10525819)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 19.  高里 実 (40788676)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 20.  賈 暁媛 (20914328)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 21.  宮西 正憲 (80542969)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 22.  SHIINA Masaaki
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 23.  SHIMA Yuko
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 11 results
  • 24.  TANAKA Hiroshi
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 25.  ITO Shuichi
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 3 results
  • 26.  緒方 一博
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 27.  浜 武継
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 28.  大塚 泰史
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 29.  吉田 瑶子
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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