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Nishino Ichizo  西野 一三

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NISHINO Ichizo  西野 一三

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Researcher Number 00332388
Other IDs
Affiliation (Current) 2025: 国立研究開発法人国立精神・神経医療研究センター, 神経研究所 疾病研究第一部, 部長
Affiliation (based on the past Project Information) *help 2015 – 2025: 国立研究開発法人国立精神・神経医療研究センター, 神経研究所 疾病研究第一部, 部長
2015: 国立研究開発法人国立精神・神経医療研究センター, その他部局等, その他
2015: 国立精神・神経医療研究センター, 神経研究所疾病研究第一部, 部長
2014: 独立行政法人国立精神・神経医療研究センター, 神経研究所 疾病研究第一部, 部長
2013 – 2014: 独立行政法人国立精神・神経医療研究センター, その他部局等, その他 … More
2013: 国立精神・神経医療研究センター神経研究所, 疾病研究第一部, 部長
2010: National Center of Neurology and Psychiatry, ・神経研究所疾病研究第一部, 部長
2009 – 2010: National Center of Neurology and Psychiatry, 神経研究所・疾病研究第一部, 部長
2008: 国立精神, 神経センター・神経研究所疾病研究第一部, 部長
2008: National Center of Neurology and Psychiatry, 神経研究所疾病研究第一部, 部長
2008: 東邦大学, 国立精神・神経センター・神経研究所疾病研究第一部, 部長
2007: 国立精神・神経センター, 神経研究所・疾病研究第一部, 部長
2007: National Institute of Neuroscience, Depertment of Neuromuscular Research, Director
2006: National Institute of Neuroscience, Department of Neuromuscular Research, Director, 神経研究所 疾病研究第一部, 部長
2006: 国立精神・神経センター, 神経研究所疾病研究第一部, 部長
2003 – 2005: NATIONAL INSTITUTE OF NEUROSCIENE, NATIONAL CENTER OF NEUROLOGY AND PSYCHIATRY (NCNP), DIRECTOR, 疾病研究第一部, 部長
2002 – 2003: 国立精神・神経センター, 神経研究所・疾病研究第一部, 部長
2001: 国立精神・神経センター, 神経研究所・疫病研究第一部, 部長 Less
Review Section/Research Field
Principal Investigator
Neurology / Medium-sized Section 52:General internal medicine and related fields / Neurology
Except Principal Investigator
Neurology / Basic Section 52020:Neurology-related / Basic Section 59020:Sports sciences-related / Pediatrics
Keywords
Principal Investigator
GNE / HIBM / DMRV / 縁取り空砲 / 縁取り空胞 / オートファジー / autophagy / rimmed vacuole / distal myopathy / rimmed vacuoles … More / Danon disease / autophagic vacuole / myopathy / lysosome / 自己貪食空砲 / 自己貧食空胞 / 遠位型ミオパチー / Danon病 / 自己貪食空胞 / ミオパチー / ライソゾーム / 間質前駆細胞 / コラーゲン / 治療 / 骨格筋 / 遺伝病 / 神経分子病態 / 筋疾患 / 神経分子病態学 … More
Except Principal Investigator
HLA / 炎症性筋疾患 / Danon病 / オートファジー / 自己貪食空胞性ミオパチー / 脳神経疾患 / 血清脂質 / スポーツ医学 / ラット / 全身冷却療法 / 免疫介在性壊死性ミオパチー / myotilin / ZASP / ミオパチー / LAMP-2 / 自己貪食空胞 / 遺伝子欠失 / 細胞・組織 / 臨床 / 筋ジストロフィー / 自己免疫性筋炎 / 抗横紋筋抗体 / 免疫関連有害事象 / PD-1ミオパチー / Kv1.4 / 横紋筋抗体 / PD-1ミオパチー / 脂質代謝 / ブピバカイン / 筋損傷 / リソソーム / 相分離 / 次世代シークエンサー / 運動後遅発性筋損傷 / 冷却療法 / 運動後筋肉痛 / 運動誘発性筋損傷 / 血清CK / 遺伝子解析 / 壊死性ミオパチー / HLA遺伝子 / 免疫関連副作用筋炎 / 病理学 / 神経科学 / 封入体筋炎 / ダノン病 / limb-girdle muscular dystrophy / myofibrillar myopathy / cDNA microarray / calpain 3 / sarcomere / Neuromuscular disorders / ミオフィプリラーミオパチー / 分子病理学 / 拡張型心筋症 / マルチミニコア / ミオフィブリラーミオパチー / 臨床遺伝学 / 肢帯型筋ジストロフィー / ミオティリン / 筋原線維性ミオパチー / cDNAマイクロアレイ / カルパイン3 / サルコメア / 神経・筋疾患 / Genetic variability / Clinical variability / Molecular Diagnosiis / Somatic mosaicism / Chromosome 4q35 / Gene deletion / Autosomal Dominant / Muscular dystrophy / 浸透率 / 常染色体優勢 / PCR法 / サザンブロット解析 / 遺伝的多様性 / 臨床的多様性 / 遺伝子診断 / 体細胞モザイク / 染色体4q35 / 常染色体優性 / ライソソーム / ライソゾーム / 発現制御 / 発現抑制 / ゲノム / 筋疾患 / メチル化 / エピゲノム / 遺伝学 / 筋病理 / 遺伝子発現 / スプライシング / long PCR法 / D4Z4リピート / Rimmed vacuoles / SIL1 / マリネスコーシェーグレン症候群 / 筋病理学 / 小児神経学 / マイクロマレイ / マクロアレイ / シグナル伝達 / 病理 / 遺伝子 / 核膜 Less
  • Research Projects

    (20 results)
  • Research Products

    (127 results)
  • Co-Researchers

    (38 People)
  •  世界最大級筋レポジトリを活用した先進的オミクス解析による自己免疫性筋炎の病態解明Principal Investigator

    • Principal Investigator
      西野 一三
    • Project Period (FY)
      2025 – 2027
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Review Section
      Medium-sized Section 52:General internal medicine and related fields
    • Research Institution
      National Center of Neurology and Psychiatry
  •  自己免疫性筋炎発症に関与する免疫メカニズムの探索

    • Principal Investigator
      大貫 優子
    • Project Period (FY)
      2023 – 2025
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52020:Neurology-related
    • Research Institution
      Tokai University
  •  Elucidation of the mechanism of protein homeostasis disruption in autophagy-related neuromuscular diseases

    • Principal Investigator
      杉江 和馬
    • Project Period (FY)
      2022 – 2024
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52020:Neurology-related
    • Research Institution
      Nara Medical University
  •  Whole-body cryotherapy in sports medicine

    • Principal Investigator
      額田 均
    • Project Period (FY)
      2022 – 2024
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 59020:Sports sciences-related
    • Research Institution
      Toho University
  •  Search for genes involved in the mechanism of immune-mediated necrotizing myopathy

    • Principal Investigator
      Ohnuki Yuko
    • Project Period (FY)
      2020 – 2022
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52020:Neurology-related
    • Research Institution
      Tokai University
  •  抗横紋筋抗体の病因論的自己抗体としての意義とPD-1ミオパチーの疾患概念の確立

    • Principal Investigator
      鈴木 重明
    • Project Period (FY)
      2020 – 2024
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Review Section
      Basic Section 52020:Neurology-related
    • Research Institution
      Keio University
  •  Whole body cryotherapy in sports medicine

    • Principal Investigator
      Nukada Hitoshi
    • Project Period (FY)
      2019 – 2021
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 59020:Sports sciences-related
    • Research Institution
      Toho University
  •  Genetic Analysis in Immune-mediated necrotizing myopathy

    • Principal Investigator
      OHNUKI Yuko
    • Project Period (FY)
      2017 – 2019
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      Tokai University
  •  Pathomechanism of autophagy system and pathomechanism in rare intractable muscle diseases

    • Principal Investigator
      Sugie Kazuma
    • Project Period (FY)
      2016 – 2018
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      Nara Medical University
  •  Elucidation of molecular pathomechanism and development of therapy for collagen VI deficiencyPrincipal Investigator

    • Principal Investigator
      NISHINO Ichizo
    • Project Period (FY)
      2014 – 2016
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Clinicopathological features and autophagic pathway of autophagic vacuolar myopathy and

    • Principal Investigator
      Sugie Kazuma
    • Project Period (FY)
      2013 – 2015
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      Nara Medical University
  •  Epigenomics and muscular dystrophy

    • Principal Investigator
      HAYASHI Yukiko
    • Project Period (FY)
      2012 – 2013
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Neurology
    • Research Institution
      Tokyo Medical University
      独立行政法人国立精神・神経医療研究センター
  •  Elucidation of pathomechanism of and development of therapy ofautophagy-related muscle disordersPrincipal Investigator

    • Principal Investigator
      NISHINO Ichizo
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Pathomechanism of SIL1-mutated Marinesco-Sjogren syndrome

    • Principal Investigator
      OKADA Mari
    • Project Period (FY)
      2007 – 2008
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Toho University
      National Center of Neurology and Psychiatry
  •  顔面肩甲上腕型筋ジストロフィーにおけるエピジェネティック変化と病態機序の解明

    • Principal Investigator
      林 由起子
    • Project Period (FY)
      2007
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Clinical and molecular studies of Emery-Dreifuss muscular dystrophy

    • Principal Investigator
      HAYASHI Yukiko
    • Project Period (FY)
      2006 – 2008
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Clarification of pathomechanism of inherited muscular disorder due to abnormality of sarcomeric proteins

    • Principal Investigator
      MINAMI Narihiro
    • Project Period (FY)
      2006 – 2007
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Research on the elucidation of molecular pathomechanism of and the development of therapy of lysosomal muscle diseases.Principal Investigator

    • Principal Investigator
      NISHINO Ichizo
    • Project Period (FY)
      2004 – 2006
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Clinical and molceulcar analyses of facioscpubhumeral muscular dystrophy

    • Principal Investigator
      HAYASHI Yukiko
    • Project Period (FY)
      2003 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      National Institute of Neuroscience, National Center of Neurology and Psychiatry
  •  The elucidation of pathomechanism and the development of therapy of myopathies with autophagic abnormalitiesPrincipal Investigator

    • Principal Investigator
      NISHINO Ichizo
    • Project Period (FY)
      2001 – 2003
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      NATIONAL INSTITUTE OF NEUROSCIENE, NATIONAL CENTER OF NEUROLOGY AND PSYCHIATRY (NCNP)

All 2024 2023 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006 2005 2004 Other

All Journal Article Presentation Book Patent

  • [Book] Rosenberg’s Molecular and Genetic Basis of Neurological and Psychiatric Disease (7th Edition)2024

    • Author(s)
      Sugie K, Nishino I
    • Publisher
      Elsevier
    • ISBN
      9780443190414
    • Data Source
      KAKENHI-PROJECT-22K07497
  • [Book] Rosenberg’s Molecular and Genetic Basis of Neurological and Psychiatric Disease, Fifth Edition2014

    • Author(s)
      Sugie K, Nishino I.
    • Total Pages
      1424
    • Publisher
      Elsevier, Amsterdam, Nederland
    • Data Source
      KAKENHI-PROJECT-25461323
  • [Book] Muscular Dystrophies. International Encyclopedia Of Public Health, 1st ed. (edited by Quah S, Heggenhougen K)2008

    • Author(s)
      Astejada M, Malicdan MCV, Nishino I
    • Publisher
      Elsevier, Amsterdam, Netherlands
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Book] Annual Review 2005 神経(柳澤信夫, 篠原幸人, 岩田 誠, 清水輝夫, 寺本明(編))2005

    • Author(s)
      西野一三
    • Total Pages
      370
    • Data Source
      KAKENHI-PROJECT-16209029
  • [Book] Annual Review 2005 神経(柳澤信夫,篠原幸人,岩田 誠,清水輝夫,寺本明(編))2005

    • Author(s)
      西野一三
    • Total Pages
      370
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16209029
  • [Journal Article] Anti-NXP2 Antibody-positive Juvenile Dermatomyositis with Characteristic Fascial Thickening on Muscle Ultrasound and Improvement with Immunotherapy2024

    • Author(s)
      Fukushima Koji、Yoshida Takeshi、Yamazaki Hiroki、Takamatsu Naoko、Nagai Takashi、Osaki Yusuke、Harada Masafumi、Nishino Ichizo、Okiyama Naoko、Sugie Kazuma、Izumi Yuishin
    • Journal Title

      Intern. Med.

      Volume: 63 Issue: 12 Pages: 1813-1817

    • DOI

      10.2169/internalmedicine.2720-23

    • ISSN
      0918-2918, 1349-7235
    • Year and Date
      2024-06-15
    • Language
      English
    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-22K07497
  • [Journal Article] Pathologic Features of Anti-Ku Myositis2024

    • Author(s)
      Munenori Oyama, Marie-Therese Holzer, Yuko Ohnuki, Yoshihiko Saito, Yukako Nishimori, Shingo Suzuki, Takashi Shiina, Sarah Leonard-Louis, Olivier Benveniste, Udo Schneider, Werner Stenzel, Ichizo Nishino, Shigeaki Suzuki, Akinori Uruha
    • Journal Title

      Neurology

      Volume: 102 Issue: 8

    • DOI

      10.1212/wnl.0000000000209268

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-23K06973
  • [Journal Article] Pathogenic role of anti-cN1A autoantibodies in sporadic inclusion body myositis2023

    • Author(s)
      Yamashita Satoshi、Tawara Nozomu、Zhang Ziwei、Nakane Shunya、Sugie Kazuma、Suzuki Naoki、Nishino Ichizo、Aoki Masashi
    • Journal Title

      Journal of Neurology, Neurosurgery & Psychiatry

      Volume: 94 Issue: 12 Pages: 1018-1024

    • DOI

      10.1136/jnnp-2023-331474

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-23K18260, KAKENHI-PROJECT-22K07497
  • [Journal Article] Association of immune‐mediated necrotizing myopathy with HLA polymorphisms2023

    • Author(s)
      Ohnuki Yuko、Suzuki Shigeaki、Uruha Akinori、Oyama Munenori、Suzuki Shingo、Kulski Jerzy K.、Nishino Ichizo、Shiina Takashi
    • Journal Title

      HLA

      Volume: 101 Issue: 5 Pages: 449-457

    • DOI

      10.1111/tan.14950

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20K07911
  • [Journal Article] Association Between HLA Alleles and Autoantibodies in Dermatomyositis Defined by Sarcoplasmic Expression of Myxovirus Resistance Protein A2023

    • Author(s)
      Munenori Oyama, Yuko Ohnuki, Akinori Uruha, Yoshihiko Saito, Yukako Nishimori, Shingo Suzuki, Michio Inoue, Jantima Tanboon, Naoko Okiyama, Takashi Shiina, Ichizo Nishino, Shigeaki Suzuki
    • Journal Title

      Journal of Rheumatology

      Volume: 50 Issue: 9 Pages: 1159-1164

    • DOI

      10.3899/jrheum.2022-1321

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-23K06973
  • [Journal Article] HLA-DRB1 allele and autoantibody profiles in Japanese patients with inclusion body myositis2020

    • Author(s)
      Oyama Munenori、Ohnuki Yuko、Inoue Michio、Uruha Akinori、Yamashita Satoshi、Yutani Sachiko、Tanboon Jantima、Nakahara Jin、Suzuki Shingo、Shiina Takashi、Nishino Ichizo、Suzuki Shigeaki
    • Journal Title

      PLOS ONE

      Volume: 15 Issue: 8 Pages: 0237890-0237890

    • DOI

      10.1371/journal.pone.0237890

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-20K07870, KAKENHI-PROJECT-20K07911, KAKENHI-PLANNED-16H06502
  • [Journal Article] Inflammatory myopathy associated with PD-1 inhibitors2019

    • Author(s)
      Seki M., Uruha A., Ohnuki Y., Kamada S., Noda T., Onda A., Ohira M., Isami A., Hiramatsu S., Hibino M., Nakane S., Noda S., Yutani S., Hanazono A., Yaguchi H., Takao M., Shiina T., Katsuno M., Nakahara J., Matsubara S., Nishino I., Suzuki S.
    • Journal Title

      Journal of Autoimmunity

      Volume: 印刷中

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K09785
  • [Journal Article] Inflammatory myopathy associated with PD-1 inhibitors.2019

    • Author(s)
      Seki M, Uruha A, Ohnuki Y, Kamada S, Noda T, Onda A, Ohira M, Isami A, Hiramatsu S, Hibino M, Nakane S, Noda S, Yutani S, Hanazono A, Yaguchi H, Takao M, Shiina T, Katsuno M, Nakahara J, Matsubara S, Nishino I, Suzuki S.
    • Journal Title

      J Autoimmun

      Volume: in press Pages: 105-113

    • DOI

      10.1016/j.jaut.2019.03.005

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K09784, KAKENHI-PLANNED-16H06502, KAKENHI-PROJECT-17K09785
  • [Journal Article] Concurrent positive anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase antibody with reducing body myopathy: Possible double trouble2019

    • Author(s)
      Tanboon Jantima、Sanmaneechai Oranee、Charuvanij Sirirat、Sangruchi Tumtip、Galindo-Feria Angeles S.、Lundberg Ingrid E.、Ohnuki Yuko、Shiina Takashi、Suzuki Shigeaki、Nishino Ichizo
    • Journal Title

      Neuromuscular Disorders

      Volume: 29 Issue: 7 Pages: 543-548

    • DOI

      10.1016/j.nmd.2019.05.007

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PLANNED-16H06502, KAKENHI-PROJECT-17K09784, KAKENHI-PROJECT-17K09785
  • [Journal Article] Small-Vessel Vasculopathy Due to Aberrant Autophagy in LAMP-2 Deficiency2018

    • Author(s)
      Nguyen Huan T.、Noguchi Satoru、Sugie Kazuma、Matsuo Yoshiyuki、Nguyen Chuyen T. H.、Koito Hitoshi、Shiojima Ichiro、Nishino Ichizo、Tsukaguchi Hiroyasu
    • Journal Title

      Scientific Reports

      Volume: 8 Issue: 1 Pages: 3326-3326

    • DOI

      10.1038/s41598-018-21602-8

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17K09719, KAKENHI-PROJECT-16K09728
  • [Journal Article] A Nationwide Survey on Danon Disease in Japan2018

    • Author(s)
      Sugie Kazuma、Komaki Hirofumi、Eura Nobuyuki、Shiota Tomo、Onoue Kenji、Tsukaguchi Hiroyasu、Minami Narihiro、Ogawa Megumu、Kiriyama Takao、Kataoka Hiroshi、Saito Yoshihiko、Nonaka Ikuya、Nishino Ichizo
    • Journal Title

      International Journal of Molecular Sciences

      Volume: 19 Issue: 11 Pages: 3507-3507

    • DOI

      10.3390/ijms19113507

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K09719, KAKENHI-PROJECT-16K09728
  • [Journal Article] Muscle Weakness and Fibrosis Due to Cell Autonomous and Non-cell Autonomous Events in Collagen VI Deficient Congenital Muscular Dystrophy2017

    • Author(s)
      Noguchi S, Ogawa M, Malicdan MC, Nonaka I, Nishino I
    • Journal Title

      EBioMedicine

      Volume: 15(2017) Pages: 193-202

    • DOI

      10.1016/j.ebiom.2016.12.011

    • Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15H04846, KAKENHI-PROJECT-26293214
  • [Journal Article] Biallelic TBCD mutations cause early-onset neurodegenerative encephalopathy2017

    • Author(s)
      Miyake N, Fukai R, Ohba C, ... Shiina M, Ogata K, Okuno-Yuguchi J, Fueki N, Ogiso Y, Suzumura H, Watabe Y, Imataka G, Leong HY, Fattal-Valevski A, Kramer U, Miyatake S, Kato M, Okamoto N, Sato Y, Mitsuhashi S, Nishino I, Kaneko N, Nishiyama A, Tamura T, Mizuguchi T, Nakashima M, Tanaka F, Saitsu H, Matsumoto N
    • Journal Title

      American Journal of Human Genetics

      Volume: 99 Issue: 4 Pages: 950-961

    • DOI

      10.1016/j.ajhg.2016.08.005

    • Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-ORGANIZER-24118001, KAKENHI-PLANNED-24118005, KAKENHI-PLANNED-24118007, KAKENHI-PROJECT-25250008, KAKENHI-PROJECT-15H04375, KAKENHI-PROJECT-16H05160, KAKENHI-PROJECT-16H05357, KAKENHI-PROJECT-26293214, KAKENHI-PROJECT-26330331, KAKENHI-PROJECT-26460373, KAKENHI-PROJECT-26461549, KAKENHI-PLANNED-24118002
  • [Journal Article] Skeletal Muscle Involvement in Antisynthetase Syndrome2017

    • Author(s)
      Noguchi Eri、Uruha Akinori、Suzuki Shigeaki、Hamanaka Kohei、Ohnuki Yuko、Tsugawa Jun、Watanabe Yurika、Nakahara Jin、Shiina Takashi、Suzuki Norihiro、Nishino Ichizo
    • Journal Title

      JAMA Neurology

      Volume: 74 Issue: 8 Pages: 992-992

    • DOI

      10.1001/jamaneurol.2017.0934

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K09784, KAKENHI-PROJECT-17K09785, KAKENHI-PLANNED-16H06502
  • [Journal Article] Immune-mediated Necrotizing Myopathy (IMNM) and HLA Polymorphisms2017

    • Author(s)
      大貫優子、鈴木重明、重成敦子、鈴木進悟、鈴木則宏、西野一三、椎名隆
    • Journal Title

      Major Histocompatibility Complex

      Volume: 24 Issue: 1 Pages: 46-53

    • DOI

      10.12667/mhc.24.46

    • NAID

      130005628689

    • ISSN
      2186-9995, 2187-4239
    • Language
      Japanese
    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K09785
  • [Journal Article] Perifascicular necrosis in anti-synthetase syndrome beyond anti-Jo-12016

    • Author(s)
      Uruha A, Suzuki S, Suzuki N, Nishino I
    • Journal Title

      Brain

      Volume: 139(Pt 9) Issue: 9 Pages: e50-e50

    • DOI

      10.1093/brain/aww125

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-26293214
  • [Journal Article] Beevor’s sign: a potential clinical marker for GNE myopathy2016

    • Author(s)
      Preethish-Kumar V, Pogoryelova O, Polavarapu K, Gayathri N, Seena V, Hudson J, Nishino I, Prasad C, Lochmuller H, Nalini A
    • Journal Title

      Eur J Neurol.

      Volume: 23(8) Issue: 8

    • DOI

      10.1111/ene.13041

    • Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26293214
  • [Journal Article] Early onset of cardiomyopathy and intellectual disability in a girl with Danon disease associated with a de novo novel mutation of the LAMP2 gene.2016

    • Author(s)
      Sugie K, Yoshizawa H, Onoue K, Nakanishi Y, Eura N, Ogawa M, Nakano T, Sakaguchi Y, Hayashi YK, Kishimoto T, Shima M, Saito Y, Nishino I, Ueno S.
    • Journal Title

      Neuropathology

      Volume: X Issue: 6 Pages: 561-565

    • DOI

      10.1111/neup.12307

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-25461323, KAKENHI-PROJECT-16K09728
  • [Journal Article] Milder forms of muscular dystrophy associated with POMGN2 mutations.2015

    • Author(s)
      Endo Y, Dong M, Noguchi S, Ogawa M, Hayashi YK, Kuru S, Sugiyama K, Nagai S, Ozasa S, Nonaka I, Nishino I
    • Journal Title

      Neurol Genet.

      Volume: 1(4) Issue: 4

    • DOI

      10.1212/nxg.0000000000000033

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-26293214
  • [Journal Article] Plasma IP-10 level distinguishes inflammatory myopathy2015

    • Author(s)
      Uruha, A., S. Noguchi, W. Sato, H. Nishimura, S. Mitsuhashi, T. Yamamura, and I. Nishino
    • Journal Title

      Neurology

      Volume: 85 Issue: 3 Pages: 293-294

    • DOI

      10.1212/wnl.0000000000001767

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24229006, KAKENHI-PROJECT-26860679, KAKENHI-PROJECT-26293214
  • [Journal Article] Danon disease: a phenotypic expression of LAMP-2 deficiency.2015

    • Author(s)
      Endo Y, Furuta A, Nishino I.
    • Journal Title

      Acta Neuropathol.

      Volume: 129 Issue: 3 Pages: 391-8

    • DOI

      10.1007/s00401-015-1385-4

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-25461323
  • [Journal Article] Allele-specific Gene Silencing of Mutant mRNA Restores Cellular Function in Ullrich Congenital Muscular Dystrophy Fibroblasts.2014

    • Author(s)
      Noguchi S, Ogawa M, Kawahara G, Malicdan MC, Nishino I
    • Journal Title

      Mol Ther Nucleic Acids

      Volume: 3 Pages: e171-e171

    • DOI

      10.1038/mtna.2014.22

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PROJECT-23390236, KAKENHI-PROJECT-26293214
  • [Journal Article] GNE myopathy: A prospective natural history study of disease progression.2014

    • Author(s)
      Mori-Yoshimura M, Oya Y, Yajima H, Yonemoto N, Kobayashi Y, Hayashi YK, Noguchi S, Nishino I, Murata M.
    • Journal Title

      Neuromuscul Disord

      Volume: 24 Issue: 5 Pages: 380-386

    • DOI

      10.1016/j.nmd.2014.02.008

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461323
  • [Journal Article] Mutation profile of the GNE gene in Japanese patients with distal myopathy with rimmed vacuoles (GNE myopathy).2014

    • Author(s)
      Cho A, et al.
    • Journal Title

      J Neurol Neurosurg Psychiatry.

      Volume: 85 Issue: 8 Pages: 914-917

    • DOI

      10.1136/jnnp-2013-305587

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23390236, KAKENHI-PROJECT-25461323
  • [Journal Article] Congenital fiber type disproportion myopathy caused by LMNA mutations.2014

    • Author(s)
      Kajino S, Ishihara K, Goto K, Ishigaki K, Noguchi S, Nonaka I, Osawa M, Nishino I, Hayashi YK
    • Journal Title

      J Neurol Sci

      Volume: 340 Issue: 1-2 Pages: 94-98

    • DOI

      10.1016/j.jns.2014.02.036

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-24390227, KAKENHI-PROJECT-24659437
  • [Journal Article] A nationwide survey on Marinesco-Sjogren syndrome in Japan.2014

    • Author(s)
      Masahide Goto, Mari Okada, Hirofumi Komaki, Kenji Sugai, Masayuki Sasaki, Satoru Noguchi, Ikuya Nonaka, Ichizo Nishino, and Yukiko K. Hayashi.
    • Journal Title

      Orphanet J Rare Diseases

      Volume: 9 Issue: 1 Pages: 58-58

    • DOI

      10.1186/1750-1172-9-58

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24390227, KAKENHI-PROJECT-24659437
  • [Journal Article] DNAJB6 myopathy in an Asian cohort and cytoplasmic/nuclear inclusions.2013

    • Author(s)
      Sato T, Hayashi YK, Oya Y, Kondo T, Sugie K, Kaneda D, Houzen H, Yabe I, Sasaki H, Noguchi S, Nonaka I, Osawa M, Nishino I.
    • Journal Title

      Neuromuscul Disord

      Volume: 23 Issue: 3 Pages: 269-276

    • DOI

      10.1016/j.nmd.2012.12.010

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461323
  • [Journal Article] Limb-girdle muscular dystrophy type 2I is not rare in Taiwan.2013

    • Author(s)
      Liang WC, Hayashi YK, Ogawa M, Wang CH, Huang WT, Nishino I, JongYJ.
    • Journal Title

      Neuromuscul Disord

      Volume: 23 Issue: 8 Pages: 675-681

    • DOI

      10.1016/j.nmd.2013.05.010

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24659437
  • [Journal Article] Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophy.2013

    • Author(s)
      Matsuura T, Kurosaki T, Omote Y, Minami N, Hayashi YK, Nishino I, Abe K.
    • Journal Title

      J Hum Genet

      Volume: 58 Issue: 8 Pages: 564-565

    • DOI

      10.1038/jhg.2013.33

    • NAID

      10031195288

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24390083, KAKENHI-PROJECT-24390227, KAKENHI-PROJECT-24659437
  • [Journal Article] Unusual presentation: unilateral arm and contralateral leg amyotrophy in facioscapulohumeral muscular dystrophy (FSHD)2013

    • Author(s)
      Sugie K, Hayashi YK, Goto K, Nishino I, Ueno S.
    • Journal Title

      Neurology

      Volume: 79 Issue: 5

    • DOI

      10.1212/wnl.0b013e3182617125

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22790826, KAKENHI-PROJECT-24659437
  • [Journal Article] Selective muscle involvement in a family affected by a second LIM domain mutation of fhl1 : An imaging study using computed tomography2012

    • Author(s)
      Komagamine T, Kawai M, Kokubun N, Miyatake S, Ogata K, Hayashi YK, Nishino I Hirata K.
    • Journal Title

      J Neurol Sci

      Volume: 318巻 Issue: 1-2 Pages: 163-167

    • DOI

      10.1016/j.jns.2012.04.007

    • Data Source
      KAKENHI-PROJECT-24659437
  • [Journal Article] 顔面肩甲上腕型筋ジストロフィーの最近の進歩2012

    • Author(s)
      林由起子,後藤加奈子,西野一三
    • Journal Title

      臨床神経学

      Volume: 52巻 Pages: 1154-1157

    • URL

      https://www.jstage.jst.go.jp/article/clinicalneurol/52/11/52_1154/_article/-char/ja/

    • Data Source
      KAKENHI-PROJECT-24659437
  • [Journal Article] Lipid Storage Myopathy2011

    • Author(s)
      Liang WC, Nishino I
    • Journal Title

      Curr Neurol Neurosci Rep 11

      Pages: 97-103

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] 自己貧食空胞性ミオパチーの病態解明と治療法開発2010

    • Author(s)
      西野一三
    • Journal Title

      臨床神経 50

      Pages: 1-6

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Lipid Storage Myopathy.2010

    • Author(s)
      Liang WC, Nishino I
    • Journal Title

      Curr Neurol Neurosci Rep

      Volume: 11 Pages: 97-103

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] The cathepsin L gene is a direct target of FOXO1 in skeletal muscle2010

    • Author(s)
      Yamazaki Y, Kamei Y, Sugita S, Akaike F, Kanai S, Miura S, Hirata Y, Troen BR, Kitamura T, Nishino I, Suganami T, Ezaki O, Ogawa Y
    • Journal Title

      Biochem J 427

      Pages: 171-178

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] 筋疾患とオートファジー2010

    • Author(s)
      本田真也, 西野一三
    • Journal Title

      BIO Clinica. 25

      Pages: 42-46

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] 筋疾患とオートファジー2010

    • Author(s)
      本田真也,西野一三
    • Journal Title

      BIO Clinica 25

      Pages: 42-46

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Autophagic degradation of nuclear components in mammalian cells2009

    • Author(s)
      Park YE, Hayashi YK, Bonne G, Arimura T, Noguchi S, Nonaka I, Nishino I
    • Journal Title

      Autophagy 5

      Pages: 795-804

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Danon 病患者17家系51例における心筋障害の臨床的特徴2009

    • Author(s)
      杉江和馬, 埜中征哉, 西野一三
    • Journal Title

      心臓 41

      Pages: 413-418

    • NAID

      130003376912

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Chapter 19 Monitoring Autophagy in Muscle Diseases2009

    • Author(s)
      Malicdan MCV, Noguchi S, Nishino I
    • Journal Title

      Methods Enzymol 453C

      Pages: 379-396

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Novel FHL1 mutations in fatal and benign reducing body myopathy2009

    • Author(s)
      Shalaby S, Hayashi YK, Nonaka I, Noguchi S, Nishino I
    • Journal Title

      Neurology 72巻

      Pages: 375-376

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Autophagic degradation of nuclear components in mammalian cells2009

    • Author(s)
      Park YE, Hayashi YK, Bonne, G, Arimura T, Noguchi S, Nonaka I, Nishino I.
    • Journal Title

      Autophagy 5巻(in press)

      Pages: 0-0

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Pompe病2009

    • Author(s)
      門間一成,西野一三
    • Journal Title

      Clinical Neuroscience 27

      Pages: 370-371

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model2009

    • Author(s)
      Malicdan MC, Noguchi S, Hayashi YK, Nonaka I, Nishino I.
    • Journal Title

      Nat med 15

      Pages: 690-695

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19591232
  • [Journal Article] Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B2009

    • Author(s)
      Park YE, Hayashi YK, Goto K, Komaki H, Hayashi Y, Inuzuka T, Noguchi S, Nonaka I, Nishino I.
    • Journal Title

      Neuromuscul Disord 19巻

      Pages: 29-36

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Danon病患者17家系51例における心筋障害の臨床的特徴2009

    • Author(s)
      杉江和馬,埜中征哉,西野一三
    • Journal Title

      心臓 41

      Pages: 413-418

    • NAID

      130003376912

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency2009

    • Author(s)
      Liang WC, Ohkuma A, Hayashi YK, Lopez LC, Hirano M, Nonaka I, Noguchi S, Chen LH, Jong YJ, Nishino I.
    • Journal Title

      Neuromuscul Disord 19巻

      Pages: 212-216

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19591232
  • [Journal Article] Pompe病2009

    • Author(s)
      門間一成, 西野一三
    • Journal Title

      Clinical Neuroscience 27

      Pages: 370-371

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Congenital myotonic dystrophy can show congenital fiber type disproportion pathology2009

    • Author(s)
      Tominaga, Hayashi YK, Goto K, Minami N, Noguchi S, Nonaka I, Miki T, Nishino I
    • Journal Title

      Acta Neuropathol 119

      Pages: 481-486

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Clinical and genetic analysis of lipid storage myopathies2009

    • Author(s)
      Ohkuma A, Noguchi S, Sugie H, Malicdan MC, Fukuda T, Shimazu K, Lopez LC, Hirano M, Hayashi YK, Nonaka I, Nishino I.
    • Journal Title

      Muscle Nerve 39巻

      Pages: 333-342

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19591232
  • [Journal Article] VMA21 deficiency causes an autophagic myopathy by compromising V-ATPase activity and lysosomal acidification2009

    • Author(s)
      Ramachandran N, Munteanu I, Wang P, Aubourg P, Rilstone JJ, Israelian N, Naranian T, Paroutis P, Guo R, Ren ZP, Nishino I, Chabrol B Pellissier JF, Minetti C, Udd B, Fardeau M, Tailor CS, Mahuran DJ, Kissel JT, Kalimo H, Levy N, Manolson MF, Ackerley CA, Minassian BA
    • Journal Title

      Cell 137

      Pages: 235-246

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRI2009

    • Author(s)
      Murakami T, Hayashi YK, Ogawa M, Noguchi S, Campbell KP, Togawa M, Inoue T, Oka A, Ohno K, Nonaka I, Nishino I
    • Journal Title

      Brain Dev 31巻

      Pages: 465-468

    • NAID

      10025580402

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Distal lipid storage myopathy due to PNPLA2 mutation2008

    • Author(s)
      Ohkuma A, Nonaka I, Malicdan MC, Noguchi S, Ohji S, Nomura K, Sugie H, Hayashi YK, Nishino I
    • Journal Title

      Neuromuscul Disord 18巻

      Pages: 671-674

    • Data Source
      KAKENHI-PROJECT-19591232
  • [Journal Article] Rigid spine syndrome caused by a novel mutation in four-and-a-half LIM domain 1 gene (FHL1)2008

    • Author(s)
      Shalaby S, Hayashi YK, Goto K, Ogawa M, Nonaka I, Noguchi S, Nishino I.
    • Journal Title

      Neuromuscul Disord 18巻

      Pages: 959-961

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] 脂質代謝異常によるミオパチー2008

    • Author(s)
      門間一成, 梁文貞, 西野一三
    • Journal Title

      医学のあゆみ 226

      Pages: 422-427

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Affixin activates Rac1 via bPIX in C2C12 myoblast2008

    • Author(s)
      Matsuda C, Kameyama K, Suzuki A, Mishima W, Yamaji S, Okamoto H, Nishino I, Hayashi YK.
    • Journal Title

      FEBS Letters 582巻

      Pages: 1189-1196

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Genotype and phenotype analyses in 136 patients with single large-scale mitochondrial DNA deletions2008

    • Author(s)
      Yamashita S, Nishino I, Nonaka I, Goto Y
    • Journal Title

      J Hum Genet 53

      Pages: 598-606

    • NAID

      10021249625

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] 酵素欠損筋疾患の新しい治療2008

    • Author(s)
      門間一成,西野一三
    • Journal Title

      メディカルバイオ 5

      Pages: 38-43

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] 縁取り空胞を伴う遠位型ミオパチーの治療法開発2008

    • Author(s)
      西野一三
    • Journal Title

      医学のあゆみ 226

      Pages: 436-440

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Diminished binding of mutated collagen VI to the extracellular matrix surrounding myocytes2008

    • Author(s)
      Kawahara G, Ogawa M, Okada M, Malicdan MCV, Goto Y, Hayashi YK, Noguchi S, Nishino I
    • Journal Title

      Muscle Nerve 38

      Pages: 1192-1195

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Diminished binding of mutated collagen VI to the extracellular matrix surrounding myocytes2008

    • Author(s)
      Kawahara G, Ogawa M, Okada M, Malicdan MC, Goto Y, Hayashi YK, Noguchi S, Nishino I.
    • Journal Title

      Muscle Nerve 38巻

      Pages: 1192-1195

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19591232
  • [Journal Article] Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan2007

    • Author(s)
      Astejada, MN, Goto K, Nagano A, Ura S, Noguchi S, Nonaka I, Nishino I, Hayashi YK
    • Journal Title

      Acta Myol 26巻

      Pages: 159-164

    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Limb-girdle muscular dystrophy due to emerin gene mutations2007

    • Author(s)
      Ura S, Hayashi YK, Goto K, Astejada MN, Murakami T, Nagato M, Ohta S, Daimon Y, Takekawa H, Hirata K, Nonaka I, Noguchi S, Nishino I
    • Journal Title

      Archives of neurology 64巻

      Pages: 1038-1041

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Reduced cell anchorage may cause sarcolemma-specific collagen VI deficiency in Ullrich disease2007

    • Author(s)
      Kawahara G, Okada M, Morone N, Ibarra CA, Nonaka I, Noguchi S, Hayashi YK, Nishino I.
    • Journal Title

      Neurology 69巻

      Pages: 1043-1049

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19591232
  • [Journal Article] Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan, Neurology2007

    • Author(s)
      Okada M, Kawahara G, Noguchi S, Sugie K, Murayama K, Nonaka I, Hayashi YK, Nishino I.
    • Journal Title

      Neurology 69巻

      Pages: 1035-1042

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19591232
  • [Journal Article] Autophagic vacuolar myopathy.2006

    • Author(s)
      Nishino I
    • Journal Title

      Semin Pediatr Neurol 13

      Pages: 90-95

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16209029
  • [Journal Article] Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuoles2006

    • Author(s)
      Ozawa R, Hayashi YK, Ogawa M, Kurokawa R, Matsumoto H, Noguchi S, Nonaka I, Nishino I
    • Journal Title

      Am J Pathol 168巻

      Pages: 907-917

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Molecular pathomechanism of distal myopathy with rimmed vacuoles.2005

    • Author(s)
      Nishino I, et al.
    • Journal Title

      Acta Myol 24

      Pages: 80-83

    • NAID

      10016918748

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16209029
  • [Journal Article] 縁取り空砲を伴う遠位型ミオパチーの原因遺伝子と分子病態2004

    • Author(s)
      西野一三
    • Journal Title

      ゲノム医学 4

      Pages: 21-26

    • Data Source
      KAKENHI-PROJECT-16209029
  • [Journal Article] Very low penetrance in 85 Japanese families with facioscapulohumeral muscular dystrophy 1A.2004

    • Author(s)
      Goto K, Nishino I, Hayashi YK.
    • Journal Title

      J Med Genet 41(1)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15590922
  • [Journal Article] Dysferlin mutation analysis in a group of Italian patients with limb-girdle muscular dystrophy and Miyoshi myopathy.2004

    • Author(s)
      Kawabe K, Goto K, Nishino I, Angelini C, Hayashi YK.
    • Journal Title

      Eur J Neurol 11(10)

      Pages: 657-661

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15590922
  • [Patent] 高GC含量反復配列増幅用長鎖ポリメラーゼチェインリアクション法およびそれを用いた顔面肩甲上腕型筋ジストロフィ診断法2004

    • Inventor(s)
      金子(後藤) 加奈子, 林 由起子, 西野 一三
    • Industrial Property Rights Holder
      財団法人ヒューマンサイエンス振興財団
    • Industrial Property Number
      2004-323942
    • Filing Date
      2004-11-08
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15590922
  • [Presentation] 皮膚筋炎とHLA多型との関連解析2023

    • Author(s)
      〇大貫優子、大山宗徳、鈴木重明、漆葉章典、重成敦子、 鈴木進悟、西野一三、椎名隆
    • Organizer
      第31回日本組織適合性学会大会
    • Data Source
      KAKENHI-PROJECT-23K06973
  • [Presentation] 皮膚筋炎とHLA-DRB1多型との関連解析2021

    • Author(s)
      大貫優子、 鈴木重明、 漆葉章典、 重成敦子、 鈴木進悟、 井上道雄、 西野一三、 椎名隆
    • Organizer
      第29回日本組織適合性学会大会
    • Data Source
      KAKENHI-PROJECT-20K07911
  • [Presentation] Association of HLA-DRB1 alleles in dermatomyositis2020

    • Author(s)
      Yuko Ohnuki, Shigeaki Suzuki, Akinori Uruha, Sachiko Yutani, Shingo Suzuki, Michio Inoue, Ichizo Nishino, Takashi Shiina
    • Organizer
      日本人類遺伝学会第65回大会
    • Data Source
      KAKENHI-PROJECT-20K07911
  • [Presentation] 日本人封入体筋炎患者におけるHLA-DRB1遺伝子多型2019

    • Author(s)
      大山宗徳、大貫優子、漆葉章典、鈴木進悟、中原仁、椎名隆、西野一三、鈴木重明
    • Organizer
      第31回日本神経免疫学会学術集会
    • Data Source
      KAKENHI-PROJECT-17K09785
  • [Presentation] Clinical characteristics, management, and outcomes of Danon disease: A nationwide survey in Japan.2018

    • Author(s)
      Sugie K, Komaki H, Onoue K, Eura N, Shiota T, Tsukaguchi H, Namatame S, Kiriyama T, Ugawa Y, Saito Y, Nonaka I, Nishino I.
    • Organizer
      The 4th Congress of the European Academy of Neurology (EAN2018)
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K09728
  • [Presentation] 封入体筋炎とHLA-DRB1多型との関連解析2018

    • Author(s)
      大貫優子、鈴木重明、漆葉章典、重成敦子、鈴木 進悟、西野一三 、椎名 隆
    • Organizer
      第27回日本組織適合性学会大会
    • Data Source
      KAKENHI-PROJECT-17K09785
  • [Presentation] Asymmetric skeletal muscle involvement in facioscapulohumeral muscular dystrophy: A neuroimaging study.2017

    • Author(s)
      Shiota T, Sugie K, Hayashi YK, Goto K, Eura N, Kiriyama T, Nonaka I, Nishino I, Ueno S.
    • Organizer
      The 23th World Congress of Neurology
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K09728
  • [Presentation] Clinical features and management of Danon disease in Japan: A nationwide survey.2017

    • Author(s)
      Sugie K, Komaki H, Onoue K, Eura N, Shiota T, Tsukaguchi H, Namatame S, Koito H, Kiriyama T, Saito Y, Ugawa Y, Ueno S, Nonaka I, Nishino I.
    • Organizer
      The 23th World Congress of Neurology
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K09728
  • [Presentation] 免疫介在性壊死性ミオパチー (IMNM)とHLA多型との関連解析2017

    • Author(s)
      大貫優子、鈴木重明、渡邊由里香、漆葉章典、重成敦子、鈴木進悟、鈴木則宏、西野一三、椎名隆
    • Organizer
      第26回日本組織適合性学会大会
    • Data Source
      KAKENHI-PROJECT-17K09785
  • [Presentation] KGS analysis in hereditary muscle disease.2015

    • Author(s)
      Nishino I
    • Organizer
      10th Japanese-French Workshop
    • Place of Presentation
      Paris, France(Institute of Myology)
    • Year and Date
      2015-07-02
    • Invited
    • Data Source
      KAKENHI-PROJECT-26293214
  • [Presentation] 皮膚筋炎の筋病理診断におけるMxA染色の有用性.2015

    • Author(s)
      西川敦子,西野一三
    • Organizer
      第56回日本神経学会学術大会
    • Place of Presentation
      新潟(朱鷺メッセ(新潟コンベンションセンター))
    • Year and Date
      2015-05-20
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26293214
  • [Presentation] ネマリンミオパチーの臨床遺伝学的解析2013

    • Author(s)
      林由起子,本村和嗣,後藤加奈子,野口 悟,宮武聡子,輿水江里子,松本直通,西野一三
    • Organizer
      第54回日本神経学会学術大会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-24659437
  • [Presentation] Mutation screening of a large cohort of nemaline myopathy2013

    • Author(s)
      Hayashi YK, Goto K, Noguchi S, Matsumoto N, Laing N, North K, Clark N, Nonaka I, Nishino I
    • Organizer
      International Congress of the World Muscle Society
    • Place of Presentation
      USA
    • Data Source
      KAKENHI-PROJECT-24659437
  • [Presentation] FHL1 Myopathies in Japan2013

    • Author(s)
      Hayashi YK, Shalaby S, Nishino I
    • Organizer
      199th ENMC International Workshop
    • Place of Presentation
      オランダ
    • Invited
    • Data Source
      KAKENHI-PROJECT-24659437
  • [Presentation] Amphiphysin 2 (BIN1) and triad defects in several forms of centronuclear myopathies2010

    • Author(s)
      Toussaint A, Maurer M, Cowling BS, Hnia K, Mohr M, Oldfors A, Schwab Y, Yis U, Maisonobe T, Stojkovic T, Laugel V, Echaniz-Laguna A, Blot S, Mandel JL, Tiret L, Nishino I, Laporte J
    • Organizer
      15th International Congress of the World Muscle Society (WMS)
    • Place of Presentation
      Kumamoto, Japan
    • Year and Date
      2010-10-13
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Recent advance in congenital muscular dystrophy2010

    • Author(s)
      西野一三
    • Organizer
      The 6th Congress of Asian Society for Pediatric Research & 51st Annual Meeting of Taiwan Pediatric Association
    • Place of Presentation
      Taipei, Taiwan
    • Year and Date
      2010-04-17
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Recent advance in congenital muscular dystrophy.2010

    • Author(s)
      Nishino I
    • Organizer
      The 6th Congress of Asian Society for Pediatric Research & 51st Annual Meeting of Taiwan Pediatric Association
    • Place of Presentation
      台北インターナショナルコンベンションセンター
    • Year and Date
      2010-04-17
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Genetic, clinical, and pathological features of congenital fiber type disproportion in Japan2010

    • Author(s)
      Tominaga K, Hayashi YK, Goto K, Minami N, Noguchi S, Nonaka I, Miki T, Nishino I
    • Organizer
      15th International Congress of the World Muscle Society (WMS)
    • Place of Presentation
      Kumamoto, Japan
    • Year and Date
      2010-10-13
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Lamp-1 overexpression rescues cardiomyopathy in Lamp-2 deficient cells by correcting cellular lysosomal function2010

    • Author(s)
      Honda S, Noguchi S, Malicdan MCV, Hayashi YK, Saftig P, Nishino I
    • Organizer
      15th International Congress of the World Muscle Society (WMS)
    • Place of Presentation
      Kumamoto, Japan
    • Year and Date
      2010-10-13
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Sialic Acid Treatment of Distal Myopathy with Rimmed Vacuoles(DMRV)2010

    • Author(s)
      西野一三
    • Organizer
      アジア・オセアニア筋学センター(AOMC)第9回年次総会
    • Place of Presentation
      Millennium Seoul Hilton(韓国ソウル)
    • Year and Date
      2010-03-26
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] A case of X-linked myopathy with excessive autophagy : the first case in Japan2010

    • Author(s)
      Kurashige T, Takahashi T, Kondo K, Nakamura T, Yamawaki T, Tsuburaya R, Hayashi YK, Nonaka I, Nishino I, Matsumoto M
    • Organizer
      15th International Congress of the World Muscle Society (WMS)
    • Place of Presentation
      Kumamoto, Japan
    • Year and Date
      2010-10-13
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Congenital form of X-linked myopathy with excessive autophagy associated with VMA21 mutation2010

    • Author(s)
      Ikeda C, Honda R, Komaki H, Sasaki M, Munteanu I, Ramachandran N, Minassian BA, Tsuburaya R, Hayashi YK, Nishino I
    • Organizer
      15th International Congress of the World Muscle Society (WMS)
    • Place of Presentation
      Kumamoto, Japan
    • Year and Date
      2010-10-13
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Sialic Acid Treatment of Distal Myopathy with Rimmed Vacuoles (DMRV)2010

    • Author(s)
      西野一三
    • Organizer
      The 9th Annual Asian and Oceanian Myology Center (AOMC) Scientific Meeting
    • Place of Presentation
      Seoul, Korea
    • Year and Date
      2010-03-26
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] 縁取り空胞を伴う遠位型ミオパチーの治療法開発2009

    • Author(s)
      西野一三, Malicdan MCV, 野口悟
    • Organizer
      第32回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜(神奈川県横浜市)
    • Year and Date
      2009-12-10
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Lamp1 overexpression may rescue cardiomyopathy in Lamp2 deficient mice2009

    • Author(s)
      Honda S, Noguchi S, Malicdan MCV, Hayashi YK, Saftig P, Nishino I
    • Organizer
      14th International Congress of the World Muscle Society (WMS)
    • Place of Presentation
      Geneva, Switzerland
    • Year and Date
      2009-09-11
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Congenital myotonic dystrophy in patients diagnosed as congenital fiber type disproportion2009

    • Author(s)
      Tominaga K, Hayashi YK, Goto K, Minami N, Noguchi S, Nonaka I, Nishino I
    • Organizer
      14th International Congress of the World Muscle Society (WMS)
    • Place of Presentation
      Geneva, Switzerland
    • Year and Date
      2009-09-11
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] 縁取り空胞を伴う遠位型ミオパチーの治療法開発2009

    • Author(s)
      西野一三,Malicdan MCV,野口悟
    • Organizer
      第32回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2009-12-10
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Sialic acid metabolites preclude the development of myopathic phenotype in the DMRV/hIBM mouse model2009

    • Author(s)
      Malicdan MCV, Noguchi S, Hayashi YK, Nonaka I, Nishino I
    • Organizer
      Congress of the World Muscle Society (WMS)
    • Place of Presentation
      Geneva, Switzerland
    • Year and Date
      2009-09-09
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] LAMP1過剰発見によるダノン病治療への試み2009

    • Author(s)
      本田真也,野口悟,Malicdan MCV,林由起子,Saftig P,西野一三
    • Organizer
      第32回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2009-12-12
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Marinesco-Sjogren syndrome due to SIL1 mutations is characterized by rimmed vacuolar myopathy with outer nuclear membrane abnormality2008

    • Author(s)
      Nishino I, 他
    • Organizer
      60th Annual Meeting of American Academy of Neurology
    • Place of Presentation
      アメリカ
    • Year and Date
      2008-04-17
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Presentation] Cytoplasmic body with acid phosphatase activity-Hallmark of adult-onset Pompe disease on muscle pathology2008

    • Author(s)
      Nishino I, Oya Y, Monma K, Noguchi S, Hayashi YK, Nonaka I
    • Organizer
      Congress of the World Muscle Society (WMS), Newcastle Upon Tyne
    • Place of Presentation
      United Kingdom
    • Year and Date
      2008-10-01
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Becker型筋ジストロフィーにおける縁取り空胞の出現に関する臨床病理学的検討2008

    • Author(s)
      門間一成,野口悟,林由起子,南成祐,元吉和夫,鎌倉恵子,埜中征哉,西野一三
    • Organizer
      第49回日本神経学会総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Novel ETFDH mutations and normal CoQ10 level in Taiwanese patients with multiple acyl-CoA dehydrogenase deficiency2008

    • Author(s)
      Liang WC, Ohkuma A, Hayashi YK, Lopez LC, Hirano M, Nonaka I, Noguchi S, Jong YJ, Nishino I
    • Organizer
      Congress of the World Muscle Society (WMS), Newcastle Upon Tyne
    • Place of Presentation
      United Kingdom
    • Year and Date
      2008-09-30
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Alpha-dystroglycanopathies in Japan2008

    • Author(s)
      Nishino I
    • Organizer
      International Workshop on Muscular Dystrophies
    • Place of Presentation
      アメリカ
    • Year and Date
      2008-05-15
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Presentation] Alpha-dystroglycanopathies in Japan2008

    • Author(s)
      Nishino I
    • Organizer
      International Workshop on Muscular Dystrophies
    • Place of Presentation
      アメリカ
    • Year and Date
      2008-05-15
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Marinesco-Sjogren syndrome is the third most common congenital muscular dystrophy in Japan2008

    • Author(s)
      Nishino I
    • Organizer
      International Workshop for Congenital Muscular Dystrophy
    • Place of Presentation
      アメリカ
    • Year and Date
      2008-07-18
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Ullrich congenital muscular dystrophy due to sarcolemma specific coallgen VI deficiency2008

    • Author(s)
      Nishino I
    • Organizer
      International Workshop for Congenital Muscular Dystrophy
    • Place of Presentation
      アメリカ
    • Year and Date
      2008-07-17
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Alpha-dystroglycanopathies in Japan2008

    • Author(s)
      西野一三
    • Organizer
      International Workshop on Muscular Dystrophies
    • Place of Presentation
      Charlotte
    • Year and Date
      2008-05-15
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Congenital myotonic dystrophy and myotubular myopathy may be differentiated by type 2C fibers and peripheral halos2008

    • Author(s)
      Fujimura C, Noguchi S, Minami N, Nonaka I, Hayashi YK, Nishino I
    • Organizer
      Congress of the World Muscle Society (WMS), Newcastle Upon Tyne
    • Place of Presentation
      United Kingdom
    • Year and Date
      2008-10-01
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Muatation analysis and response to riboflavin therapy in Taiwanese MADD patients2008

    • Author(s)
      Liang WC, Ohkuma A, Goto K, Hayashi YK, Jong YJ, Nishino I
    • Organizer
      第50回日本小児神経学会総会
    • Place of Presentation
      東京
    • Year and Date
      2008-05-29
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] RYR1-related core and non-core myopathies2008

    • Author(s)
      西野一三
    • Organizer
      Myology 2008
    • Place of Presentation
      Marseille
    • Year and Date
      2008-05-29
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Fukuyama congenital muscular dystrophy. International Workshop for Congenital Muscular Dystrophy2008

    • Author(s)
      Nishino I
    • Organizer
      International Workshop for Congenital Muscular Dystrophy
    • Place of Presentation
      アメリカ
    • Year and Date
      2008-07-17
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Fukuyama congenital muscular dystrophy2008

    • Author(s)
      西野一三
    • Organizer
      International Workshop for Congenital Muscular Dystrophy
    • Place of Presentation
      Iowa City
    • Year and Date
      2008-07-17
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Cytoplasmic body with acid phosphatase activity-Hallmark of adult-onset Pompe disease on muscle pathology2008

    • Author(s)
      Nishino I, 他
    • Organizer
      Congress of the World Muscle Society (WMS)
    • Place of Presentation
      イギリス
    • Year and Date
      2008-10-01
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] RYR1-related core and non-core myopathies2008

    • Author(s)
      Nishino I
    • Organizer
      Myology 2008
    • Place of Presentation
      フフンス
    • Year and Date
      2008-05-29
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Marinesco-Sjogren syndrome is the third most common congenital muscular dystrophy in Japan2008

    • Author(s)
      西野一三
    • Organizer
      International Workshop for Congenital Muscular Dystrophy
    • Place of Presentation
      Iowa City
    • Year and Date
      2008-07-18
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Ullrich congenital muscular dystrophy due to sarcolemma specific coallgen VI deficiency2008

    • Author(s)
      西野一三
    • Organizer
      International Workshop for Congenital Muscular Dystrophy
    • Place of Presentation
      Iowa City
    • Year and Date
      2008-07-17
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Activation of mesenchymal progenitor cells in skeletal muscles of Collagen VI deficient mice.

    • Author(s)
      Noguchi S, Ogawa M, Nishino I:
    • Organizer
      19th International Congress of the World Muscle Society
    • Place of Presentation
      Berlin, Germany (福岡国際会議場)
    • Year and Date
      2014-10-07 – 2014-10-11
    • Data Source
      KAKENHI-PROJECT-26293214
  • [Presentation] A nationwide survey of Danon disease in Japan.

    • Author(s)
      Sugie K, Komaki H, Eura N, Nonaka I, Ueno S, Nishino I.
    • Organizer
      The 13th International Congress on Neuromuscular Diseases (ICNMD XIII)
    • Place of Presentation
      フランス・ニース
    • Year and Date
      2014-07-05 – 2014-07-10
    • Data Source
      KAKENHI-PROJECT-25461323
  • 1.  NOGUCHI Satoru (00370982)
    # of Collaborated Projects: 8 results
    # of Collaborated Products: 37 results
  • 2.  HAYASHI Yukiko (50238135)
    # of Collaborated Projects: 7 results
    # of Collaborated Products: 42 results
  • 3.  OHNUKI Yuko (20384927)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 10 results
  • 4.  鈴木 重明 (50276242)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 12 results
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    # of Collaborated Projects: 3 results
    # of Collaborated Products: 21 results
  • 6.  GOTO Kanako (00392415)
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    # of Collaborated Products: 5 results
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    # of Collaborated Products: 7 results
  • 12.  OKADA Mari (80328046)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 13.  KUBOTA Takeo (70293511)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 14.  MURAKAMI Nobuyuki (00316598)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 15.  MINAMI Narihiro (20392417)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 16.  西川 敦子 (70737262)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 17.  山下 賢 (20457592)
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    # of Collaborated Products: 1 results
  • 18.  森 英一朗 (70803659)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 19.  北野 滋久 (60402682)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 20.  中根 俊成 (70398022)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 21.  HONDA Shinya
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 6 results
  • 22.  TOMINAGA Kayo
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 23.  MONMA Kazunari
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 6 results
  • 24.  KIYONO Chieko
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 25.  SATO Hidenori
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 26.  SATO Takatoshi
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 27.  ISHIYAMA Teruhiko
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 28.  AMANAKA Kohei
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 29.  ISHI Shunsuke
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 30.  TANAKA Kiyoji
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 31.  SATO Fumitoshi
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 32.  SUZUKI Naoki
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 33.  山村 隆
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 34.  塚口 裕康
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 35.  松浦 徹
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 36.  緒方 一博
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 37.  松本 直通
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 38.  青木 正志
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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