Kondo Hiroyuki 近藤寛之

… Alternative Names

KONDO Hiroyuki 近藤寛之

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Researcher Number	40268991
External Links
Affiliation (Current)	2025: 産業医科大学, 医学部, 教授
Affiliation (based on the past Project Information) *help	2017 – 2024: 産業医科大学, 医学部, 教授 2013 – 2015: 産業医科大学, 医学部, 教授 2009 – 2012: Fukuoka University, 医学部, 准教授 2007 – 2008: Fukuoka University, 医学部, 講師 2003 – 2005: 福岡大学, 医学部, 講師
Review Section/Research Field	Principal Investigator Ophthalmology / Basic Section 56060:Ophthalmology-related Except Principal Investigator Basic Section 56060:Ophthalmology-related / Ophthalmology
Keywords	Principal Investigator 家族性滲出性硝子体網膜症 / 遺伝子 / 網膜剥離 / WNTシグナル / Stickler症候群 / 遺伝子診断 / 転写活性 / 黄斑低形成 / OCT / COL2A1 … More / 網膜疾患 / TSPAN12 / 未熟児網膜症 / 機能解析 / 遺伝形式 / Norrin/wntシグナル / ルシフェラーゼアッセイ / 孤発例 / microRNA / エクソソーム / ルシフェラーゼ / ノックダウン / FRMD7 / GPR143 / SLC38A8 / トランス活性ドメイン / siRNA / 全エクソームシークエンス / PAX6 / 遺伝学 / 医療・福祉 / 視力 / 視野 / 光干渉断層計 / 眼底自発蛍光 / 網膜電図 / 光干渉断層 / COL2A1遺伝子 / 遺伝子解析 / 網膜剥離の予防 / 網膜変性 / 臨床診断 / familial optic atrophy / retinitis pigmentosa / familial exudative vitreoretinopathy / autosomal recessive / microsatellite marker / genetic diagnosis / human genome / retinal disease / 常染色体劣性遺伝 / 家族性視神経萎縮 / 網膜色素変性症 / 常染色体劣性 / マイクロサテライトマーカ / ヒトゲノム / 視神経 / TOPFALSH / SuperTOPFLASH / 血管形成 / 遺伝子変異 / レポーターアッセイ / CTNNB1 / 遺伝子異常 / GPR180 / 小瞳孔 / KIF11 / ATOH7 / ZNF408 / Norrie病 / 血管内皮成長因子 / 網膜 / 小児 / VEGF / 血管内皮増殖因子 / NDP遺伝子 / Coats病 / SuperTopflash / PAX3 / 新生血管 / ノリエ病 … More Except Principal Investigator 方法論 / 希少疾患 / 疫学 / データベース / 網膜疾患 / 遺伝子検索 / 遺伝性視神経ジストロフィ / 網膜電図 / 網膜色素変性 / 全ゲノム解析 / 光干渉断層計検査(OCT) / 網膜電図(ERG) / KCNV2 / ABCA4 / 先天網膜分離症 / 遺伝性網膜ジストロフィ / 遺伝子解析 / 未診断眼疾患 / 遺伝子診断 / 未診断眼疾患患者 / ターゲットシークエンス解析 / 次世代シークエンサー / 変異解析 / 希少眼疾患 / peroxiredoxin / 緑内障遺伝子 / 細胞マトリックス / c-myc / sirt1 / 劇症型未熟児網膜症 / 線維柱帯細胞 / Dynamic contour tonometer / ケルセチン / 抗VEGF抗体 / 視神経乳頭ピット / 細胞外マトリックス / ステロイド緑内障 / 酸化ストレス / 線維柱帯 / 緑内障 Less

大規模医療データベースを用いた希少性網膜疾患の疫学研究に関する方法論的検討
- Principal Investigator
  
  落合信寿
- Project Period (FY)
  2024 – 2027
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56060:Ophthalmology-related
- Research Institution
  University of Occupational and Environmental Health, Japan
Genetic and molecular study for isolated familial exudative vitreoretinopathyPrincipal Investigator
- Principal Investigator
  
  近藤寛之
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56060:Ophthalmology-related
- Research Institution
  University of Occupational and Environmental Health, Japan
遺伝性網膜・視神経ジストロフィの症例収拾および疾患別頻度の検討
- Principal Investigator
  
  國吉一樹
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56060:Ophthalmology-related
- Research Institution
  Kindai University
Clinical and molecular investigation on foveal hypoplasiaPrincipal Investigator
- Principal Investigator
  
  Hiroyuki Kondo
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56060:Ophthalmology-related
- Research Institution
  University of Occupational and Environmental Health, Japan
Clinical and genetic research for the treatment of retinal detachment in Stickler syndromePrincipal Investigator
- Principal Investigator
  
  Kondo Hiroyuki
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  University of Occupational and Environmental Health, Japan
Construction of a comprehensive regional medical system and development of diagnostic method for rare and undiagnosed eye disease patients in Japan
- Principal Investigator
  
  Hotta Yoshihiro
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Hamamatsu University School of Medicine
Genetic variations and functions in familial exudative vitreoretinopathyPrincipal Investigator
- Principal Investigator
  
  KONDO Hiroyuki
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  University of Occupational and Environmental Health, Japan
Pathogenesisof Coats disease: establishing a concept of pediatric retinal detachmentPrincipal Investigator
- Principal Investigator
  
  KONDO Hiroyuki
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  University of Occupational and Environmental Health, Japan
MOLECULAR BIOLOGICAL STUDIES IN DEVELOPMENT OF GLAUCOMA
- Principal Investigator
  
  TAWARA Akihiko
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  University of Occupational and Environmental Health, Japan
Genetic study for diseases of insufficient development of retinal vesselsPrincipal Investigator
- Principal Investigator
  
  KONDO Hiroyuki
- Project Period (FY)
  2007 – 2009
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Fukuoka University
Development of a comprehensive system of linkage analysis for identification of hereditary retinal disease genes using genomic informationPrincipal Investigator
- Principal Investigator
  
  KONDO Hiroyuki
- Project Period (FY)
  2003 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Ophthalmology
- Research Institution
  Fukuoka University

[Book] A quick quide to pediatric retina2021
- Author(s)
  Hiroyuki Kondo
- Total Pages
  5
- Publisher
  Springer Nature SIngapore
- Data Source
  KAKENHI-PROJECT-20K09818
[Book] A quick quide to pediatric retina2021
- Author(s)
  Kondo Hiroyuki
- Publisher
  Springer Nature SIngapore
- ISBN
  9789811565519
- Data Source
  KAKENHI-PROJECT-20K09818
[Book] 今日の治療指針　私はこう治療している20162016
- Author(s)
  近藤寛之
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-25462743
[Book] 一目でわかる眼疾患の見分け方　ぶどう膜疾患、網膜・硝子体疾患2016
- Author(s)
  近藤寛之
- Publisher
  メジカルビュー社
- Data Source
  KAKENHI-PROJECT-25462743
[Book] 小児眼科学2015
- Author(s)
  近藤寛之
- Publisher
  三輪書店
- Data Source
  KAKENHI-PROJECT-25462743
[Book] どうとる？どう読む？ERG2015
- Author(s)
  近藤寛之
- Total Pages
  4
- Publisher
  Medical View
- Data Source
  KAKENHI-PROJECT-25462743
[Book] 網膜剥離と極小切開硝子体手術〈眼科臨床エキスパート〉2015
- Author(s)
  近藤寛之
- Total Pages
  8
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-25462743
[Book] 専門医のための眼科臨床クオリファイ2013
- Author(s)
  近藤寛之
- Total Pages
  8
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-25462743
[Book] 臨床糖尿病マニュアル改訂第3版2012
- Author(s)
  近藤寛之
- Total Pages
  482
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-22591956
[Book] 専門医のための眼科臨床クオリファイ2012
- Author(s)
  近藤寛之
- Total Pages
  8
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-22591956
[Book] 臨床糖尿病マニュアル改訂第３版2012
- Author(s)
  近藤寛之
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-22591956
[Book] 眼科手術学：網膜・硝子体II2012
- Author(s)
  近藤寛之
- Publisher
  文光堂
- Data Source
  KAKENHI-PROJECT-22591956
[Book] Eye Surgery Now 6きれいな小児眼科手術これであなたも悩まない!2011
- Author(s)
  近藤寛之
- Total Pages
  6
- Publisher
  メジカルビュー社
- Data Source
  KAKENHI-PROJECT-22591956
[Book] 専門医のための眼科臨床クオリファイ8網膜血管障害2011
- Author(s)
  近藤寛之
- Total Pages
  256
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-22591956
[Book] Eye Surgery Now 6 きれいな小児眼科手術これであなたも悩まない!2011
- Author(s)
  近藤寛之
- Total Pages
  153
- Publisher
  メジカルビュー社
- Data Source
  KAKENHI-PROJECT-22591956
[Book] 専門医のための眼科臨床クオリファイ9こどもの眼と疾患2011
- Author(s)
  近藤寛之
- Total Pages
  286
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-22591956
[Book] 眼科手術学:網膜・硝子体II2010
- Author(s)
  近藤寛之
- Total Pages
  336
- Publisher
  文光堂
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] Genetic and clinical features of ABCA4-associated retinopathy in a Japanese nationwide cohort2024
- Author(s)
  Kei Mizobuchi1 Takaaki Hayashi, Koji Tanaka, Kazuki Kuniyosh4, Yusuke Murakami, Natsuko Nakamura, Kaoruko Torii, Atsushi Mizota, Daiki Sakai, Akiko Maeda, Taro Kominami, Shinji Ueno, Shunji Kusaka, Koji M Nishiguchi, Yasuhiro Ikeda, Mineo Kondo, Kazushige Tsunoda, Yoshihiro Hotta, Tadashi Nakano
- Journal Title
  
  Am J Ophthalmol.
  
  Volume: 16:264 Pages: 36-43
- DOI
  10.1016/j.ajo.2024.03.007
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K09712, KAKENHI-PROJECT-22K09788, KAKENHI-PROJECT-22K09825
[Journal Article] Familial exudative vitreoretinopathy with and without pathogenic variants of Norrin/β-catenin signaling genes2024
- Author(s)
  Kondo Hiroyuki、Tsukahara-Kawamura Tomoko、Matsushita Itsuka、Nagata Tatsuo、Hayashi Takaaki、Nishina Sachiko、Higasa Koichiro、Uchio Eiichi、Kondo Mineo、Sakamoto Taiji、Kusaka Shunji
- Journal Title
  
  Ophthalmology Science
  
  Volume: in press Issue: 5 Pages: 100514-100514
- DOI
  10.1016/j.xops.2024.100514
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K09053
[Journal Article] EFFICACY OF INNER WALL RETINECTOMY FOR BULLOUS SCHISIS CAVITY HANGING OVER OR THREATENING THE MACULA IN PATIENTS WITH CONGENITAL X-LINKED RETINOSCHISIS2023
- Author(s)
  Iwahashi C, Matsushita I, Kuniyoshi K, Kondo H, Kusaka S
- Journal Title
  
  Rretina
  
  Volume: 43 Issue: 1 Pages: 64-71
- DOI
  10.1097/iae.0000000000003633
- Data Source
  KAKENHI-PROJECT-22K09825
[Journal Article] Optical coherence tomography findings of the peripheral retina in patients with congenital X-linked retinoschisis2023
- Author(s)
  Nakajima, A., Kuniyoshi, K., Iwahashi, C., Mano, F., Hayashi, T., Kondo, H., Mizobuchi, K., Matsushita, I., Suga, A., Yoshitake, K., Nakano, T., Iwata, T., Matsumoto, C. and Kusaka, S.
- Journal Title
  
  Frontiers in Medicine
  
  Volume: 10 Pages: 1280564-1280564
- DOI
  10.3389/fmed.2023.1280564
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K09825
[Journal Article] Severe foveal hypoplasia and macular degeneration in Stickler syndrome caused by missense mutation in <i>COL2A1</i> gene2022
- Author(s)
  Asano Mamika、Yokoyama Katsuhiko、Oku Kazuma、Matsushita Itsuka、Kimoto Kenichi、Kubota Toshiaki、Kondo Hiroyuki
- Journal Title
  
  Ophthalmic Genetics
  
  Volume: 43 Issue: 4 Pages: 508-512
- DOI
  10.1080/13816810.2022.2068044
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K09818
[Journal Article] Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole‐exome sequencing2022
- Author(s)
  Suga Akiko、Yoshitake Kazutoshi、Fukuchi Takeo、Hatase Tetsuhisa、Horiguchi Masayuki、Shimada Yoshiaki、Tanikawa Atsuhiro、Yamamoto Shuichi、Miura Gen、Ito Nana、Murakami Akira、Fujimaki Takuro、Hotta Yoshihiro、Tanaka Koji、Iwata Takeshi、他
- Journal Title
  
  Human Mutation
  
  Volume: 43 Issue: 12 Pages: 2251-2264
- DOI
  10.1002/humu.24492
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K09825, KAKENHI-PROJECT-21K09756, KAKENHI-PROJECT-22K09764, KAKENHI-PROJECT-22K09788, KAKENHI-PROJECT-22K09825, KAKENHI-PROJECT-18K09432, KAKENHI-PROJECT-20K09818
[Journal Article] Identification of Interphotoreceptor retinoid-binding protein in the Schisis cavity fluid of a patient with congenital X-linked Retinoschisis2022
- Author(s)
  Mano F, Sugioka K, Kuniyoshi K, Kondo H, Kusaka S
- Journal Title
  
  BMC Ophthalmol
  
  Volume: 22 Issue: 1 Pages: 14-14
- DOI
  10.1186/s12886-021-02234-5
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K09825
[Journal Article] 小児眼科疾患　はじめの一歩　特集こども眼科外来　はじめの一歩ー乳児から小児までー2021
- Author(s)
  近藤寛之
- Journal Title
  
  OCULISTA
  
  Volume: 98 Pages: 50-58
- Data Source
  KAKENHI-PROJECT-20K09818
[Journal Article] Homozygous single nucleotide duplication of SLC38A8 in autosomal recessive foveal hypoplasia: The first Japanese case report2021
- Author(s)
  Hayashi Takaaki、Kondo Hiroyuki、Matsushita Itsuka、Mizobuchi Kei、Baba Akinori、Iida Kie、Kubo Hiroyuki、Nakano Tadashi
- Journal Title
  
  Documenta Ophthalmologica
  
  Volume: 143 Issue: 3 Pages: 323-330
- DOI
  10.1007/s10633-021-09842-y
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K09818, KAKENHI-PROJECT-21K09756
[Journal Article] Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in <i>KIF11</i> Gene2021
- Author(s)
  Kondo Hiroyuki、Matsushita Itsuka、Nagata Tatsuo、Fujihara Etsuko、Hosono Katsuhiro、Uchio Eiichi、Hotta Yoshihiro、Kusaka Shunji
- Journal Title
  
  Translational Vision Science & Technology
  
  Volume: 10 Issue: 7 Pages: 18-18
- DOI
  10.1167/tvst.10.7.18
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K09818, KAKENHI-PROJECT-20K09825
[Journal Article] 小児期に遭遇する網膜ジストロフィ（特集・網膜色素変性のアップデート）2021
- Author(s)
  近藤寛之
- Journal Title
  
  臨床眼科
  
  Volume: 75 Pages: 1501-1510
- Data Source
  KAKENHI-PROJECT-20K09818
[Journal Article] 総説87 黄斑低形成（専門医制度・生涯教育講座）2021
- Author(s)
  近藤寛之
- Journal Title
  
  日眼会誌
  
  Volume: 125 Pages: 695-708
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K09818
[Journal Article] Ultra-wide field fundus autofluorescence imaging of eyes with Stickler syndrome2020
- Author(s)
  Fujimoto Kazushi、Nagata Tatsuo、Imagawa Mamika、Oku Kazuma、Matsushita Itsuka、Hayashi Takaaki、Kimoto Kennichi、Kuniyoshi Kazuki、Ohji Masahito、Kusaka Shunji、Kondo Hiroyuki
- Journal Title
  
  Retina
  
  Volume: in press
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11441
[Journal Article] ULTRA-WIDE FIELD FUNDUS AUTOFLUORESCENCE IMAGING OF EYES WITH STICKLER SYNDROME2020
- Author(s)
  Fujimoto Kazushi、Nagata Tatsuo、Matsushita Itsuka、Oku Kazuma、Imagawa Mamika、Kuniyoshi Kazuki、Hayashi Takaaki、Kimoto Kenichi、Ohji Masahito、Kusaka Shunji、Kondo Hiroyuki
- Journal Title
  
  Retina
  
  Volume: 41 Issue: 3 Pages: 638-645
- DOI
  10.1097/iae.0000000000002879
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K09818, KAKENHI-PROJECT-21K09756
[Journal Article] Autosomal dominant foveal hypoplasia without visible macular abnormalities and PAX6 mutations2020
- Author(s)
  Matsushita Itsuka、Morita Hirofumi、Kondo Hiroyuki
- Journal Title
  
  Japanese Journal of Ophthalmology
  
  Volume: 64 Issue: 6 Pages: 635-641
- DOI
  10.1007/s10384-020-00766-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K09818
[Journal Article] Novel mutations in the RS1 gene in Japanese patients with X-linked congenital retinoschisis2019
- Author(s)
  Kondo Hiroyuki、Oku Kazuma、Katagiri Satoshi、Hayashi Takaaki、Nakano Tadashi、et al.
- Journal Title
  
  Human Genome Variation
  
  Volume: 6 Issue: 1 Pages: 3-3
- DOI
  10.1038/s41439-018-0034-6
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11434, KAKENHI-PROJECT-17K19721, KAKENHI-PROJECT-18H02954, KAKENHI-PROJECT-17H06276, KAKENHI-PROJECT-16H06269, KAKENHI-PROJECT-16KK0193, KAKENHI-PROJECT-19K09989, KAKENHI-PROJECT-17K11441
[Journal Article] Early vitrectomy to reverse macular dragging in a one-month-old boy with familial exudative vitreoretinopathy.2019
- Author(s)
  Iwata A, Kusaka S, Ishimaru M, Kondo H, Kuniyoshi K.
- Journal Title
  
  Am J Ophthalmol Case Rep
  
  Volume: 15 Pages: 10041-10041
- DOI
  10.1016/j.ajoc.2019.100493
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11440, KAKENHI-PROJECT-17K11441
[Journal Article] Electroretinograms of eyes with Stickler syndrome2019
- Author(s)
  Kondo Hiroyuki、Fujimoto Kazushi、Imagawa Mamika、Oku Kazuma、Matsushita Itsuka、Hayashi Takaaki、Nagata Tatsuo
- Journal Title
  
  Doc Ophthalmol
  
  Volume: 2019/11/30Epub Issue: 3 Pages: 233-243
- DOI
  10.1007/s10633-019-09739-x
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11441, KAKENHI-PROJECT-20K09818
[Journal Article] Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy.2018
- Author(s)
  Katagiri S, Iwasa M, Hayashi T, Hosono K, Yamashita T, Kuniyoshi K, Ueno S, Kondo M, Ueyama H, Ogita H, Shichida Y, Inagaki H, Kurahashi H, Kondo H, Ohji M, Hotta Y, Nakano T.
- Journal Title
  
  Sci Rep
  
  Volume: 8 Issue: 1 Pages: 11507-11507
- DOI
  10.1038/s41598-018-29891-9
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08627, KAKENHI-PROJECT-17K11434, KAKENHI-PROJECT-17K11447, KAKENHI-PROJECT-17K19721, KAKENHI-PROJECT-16H02515, KAKENHI-PROJECT-18H02954, KAKENHI-PROJECT-17F17418, KAKENHI-PROJECT-16K07437, KAKENHI-PROJECT-16K11284
[Journal Article] Risk allele of the FZD4 gene for familial exudative vitreoretinopathy2018
- Author(s)
  Kondo H, Uchio E, Kusaka S, Higasa K
- Journal Title
  
  Ophthalmic Genet
  
  Volume: 39 Issue: 3 Pages: 405-406
- DOI
  10.1080/13816810.2017.1401090
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K10911, KAKENHI-PROJECT-17K11441, KAKENHI-PROJECT-17K07255
[Journal Article] 高解像度OCTでみえてくるもの：新しい黄斑低形成の概念2018
- Author(s)
  近藤寛之
- Journal Title
  
  日本の眼科
  
  Volume: 89 Pages: 326-327
- Data Source
  KAKENHI-PROJECT-17K11441
[Journal Article] Lack of FOXE3 coding mutation in a case of congenital aphakia2018
- Author(s)
  Sano Yusuke、Matsukane Yusuke、Watanabe Akihisa、Sonoda Ko-hei、Kondo Hiroyuki
- Journal Title
  
  Ophthalmic Genetics
  
  Volume: 39 Issue: 1 Pages: 95-98
- DOI
  10.1080/13816810.2017.1350722
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11441
[Journal Article] Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing2018
- Author(s)
  Hosono Katsuhiro、Nishina Sachiko、Yokoi Tadashi、Katagiri Satoshi、Saitsu Hirotomo、Kurata Kentaro、Miyamichi Daisuke、Hikoya Akiko、Mizobuchi Kei、Nakano Tadashi、Minoshima Shinsei、Fukami Maki、Kondo Hiroyuki、Sato Miho、Hayashi Takaaki、Azuma Noriyuki、Hotta Yoshihiro
- Journal Title
  
  Scientific Reports
  
  Volume: 8 Issue: 1 Pages: 8279-8279
- DOI
  10.1038/s41598-018-26524-z
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11434, KAKENHI-PROJECT-17K11441, KAKENHI-PROJECT-17K11447, KAKENHI-PROJECT-17K11479, KAKENHI-PROJECT-16K11284, KAKENHI-PROJECT-16K11309
[Journal Article] Foveal Hypoplasia in Patients with Stickler Syndrome2017
- Author(s)
  Matsushita I, Nagata T, Hayashi T, Kimoto K, Kubota T, Ohji M, Kusaka S, Kondo H.
- Journal Title
  
  Ophthalmology
  
  Volume: in press Issue: 6 Pages: 896-902
- DOI
  10.1016/j.ophtha.2017.01.046
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25462738, KAKENHI-PROJECT-26870788, KAKENHI-PROJECT-17K11434, KAKENHI-PROJECT-17K11441
[Journal Article] Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR2017
- Author(s)
  Panagiotou Evangelia S.、Sanjurjo Soriano Carla、Poulter James A.、Lord Emma C.、Dzulova Denisa、Kondo Hiroyuki、Hiyoshi Atsushi、Chung Brian Hon-Yin、Chu Yoyo Wing-Yiu、Lai Connie H.Y.、Tafoya Mark E.、Karjosukarso Dyah、Collin Rob W.J.、Topping Joanne、Downey Louise M.、Ali Manir、Inglehearn Chris F.、Toomes Carmel
- Journal Title
  
  Am J Hum Genet
  
  Volume: 100 Issue: 6 Pages: 960-968
- DOI
  10.1016/j.ajhg.2017.05.001
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11441
[Journal Article] Mutations in ATOH7 gene in patients with nonsyndromic congenital retinal nonattachment and familial exudative vitreoretinopathy2016
- Author(s)
  Kondo H., Matsushita I., Tahira T., Uchio E., Kusaka S.
- Journal Title
  
  Ophthalmic Genet
  
  Volume: 印刷中
- Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25462743
[Journal Article] Novel mutations in COL2A1 gene in Japanese patients with Stickler syndrome2016
- Author(s)
  Kondo H., Matsushita I., Nagata T., Hayashi T., Kakinoki M., Uchio E., Kondo M., Ohji M., Kusaka S.
- Journal Title
  
  Hum Genome Var
  
  Volume: 印刷中
- NAID
  120006546337
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25462743
[Journal Article] Complex genetics of familial exudative vitreoretinopathy and related pediatric retinal detachment2015
- Author(s)
  Kondo H.
- Journal Title
  
  Taiwan J Ophthalmol
  
  Volume: 5 Pages: 56-62
- Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25462743
[Journal Article] 遺伝性網膜疾患に対する外科治療（遺伝性網膜疾患に対するトータルケア）2015
- Author(s)
  近藤寛之
- Journal Title
  
  臨床眼科
  
  Volume: 69 Pages: 1624-1629
- Data Source
  KAKENHI-PROJECT-25462743
[Journal Article] 家族性滲出性硝子体網膜症（FEVR）　特集発生学からみた眼の先天奇形2015
- Author(s)
  近藤寛之
- Journal Title
  
  眼科
  
  Volume: 57 Pages: 133-141
- NAID
  40020365654
- Data Source
  KAKENHI-PROJECT-25462743
[Journal Article] これだけは押さえたい遺伝性網膜硝子体疾患「知っておきたい小児眼科の最新知識３」2015
- Author(s)
  近藤寛之
- Journal Title
  
  臨床眼科
  
  Volume: 69 Pages: 278-283
- Data Source
  KAKENHI-PROJECT-25462743
[Journal Article] 未熟児網膜症（ROP)、大規模臨床試験一挙紹介2015
- Author(s)
  近藤寛之
- Journal Title
  
  Retina Medicine
  
  Volume: 4
- Data Source
  KAKENHI-PROJECT-25462743
[Journal Article] Submicroscopic deletions at 13q32.1 cause congenital microcoria2015
- Author(s)
  Fares-Taie, L. Gerber, S. Tawara, A. Ramirez-Miranda, A. Douet, J. Y. Verdin, H. Guilloux, A. Zenteno, J. C. Kondo, H. Moisset, H. Passet, B. Yamamoto, K. Iwai, M. Tanaka, T. Nakamura, Y. Kimura, W. Bole-Feysot, C. Vilotte, M. Odent, S. Vilotte, J. L. Munnich, A. Regnier, A. Chassaing, N. et al.
- Journal Title
  
  Am J Hum Genet
  
  Volume: 96 Issue: 4 Pages: 631-9
- DOI
  10.1016/j.ajhg.2015.01.014
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-25462743, KAKENHI-PROJECT-15K05577, KAKENHI-PROJECT-221S0002
[Journal Article] 混合型第一次硝子体過形成遺残に対する水晶体温存硝子体茎切断術2014
- Author(s)
  渡辺晃久近藤寛之田原昭彦金海美和後藤美和子
- Journal Title
  
  眼科手術
  
  Volume: 27 Pages: 253-256
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25462743
[Journal Article] Identification of causative pathogens in eyes with bacterial conjunctivitis by bacterial cell count and microbiota analysis2013
- Author(s)
  Aoki R, Kondo H
- Journal Title
  
  Ophthalmology
  
  Volume: (120) Pages: 668-676
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] Identification of causative pathogens in eyes with bacterial conjunctivitis by bacterial cell count and microbiota analysis2013
- Author(s)
  Aoki R, Kondo H　（7名中5番目）
- Journal Title
  
  Ophthalmology
  
  Volume: 120 Issue: 4 Pages: 668-676
- DOI
  10.1016/j.ophtha.2012.10.001
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity2013
- Author(s)
  Kondo H
- Journal Title
  
  Mol Vis
  
  Volume: (19) Pages: 476-485
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature2013
- Author(s)
  Collin, R. W., Nikopoulos, K., Dona, M., et al. (他23名)
- Journal Title
  
  Proc. Natl. Acad. Sci. USA
  
  Volume: 110(24) Issue: 24 Pages: 9856-9861
- DOI
  10.1073/pnas.1220864110
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24657005, KAKENHI-PROJECT-25462743
[Journal Article] Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity2013
- Author(s)
  Kondo H　（6名中筆頭）
- Journal Title
  
  Molecular Vision
  
  Volume: 19 Pages: 476-485
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] Familial acorea, microphthalmia and cataract syndrome2013
- Author(s)
  Kondo, H., Tahira, T., Yamamoto, K., Tawara, A.
- Journal Title
  
  Br J Ophthalmol
  
  Volume: 97 Issue: 9 Pages: 1155-60
- DOI
  10.1136/bjophthalmol-2013-303165
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25462743
[Journal Article] 未熟児網膜症に対する抗VEGF療法の効果の検討2012
- Author(s)
  渡辺晃久、近藤寛之, 他
- Journal Title
  
  眼科手術
  
  Volume: 25 Pages: 115-119
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] 小眼球症に伴う眼窩発育異常の画像評価2012
- Author(s)
  仁科幸子、近藤寛之（6名中5番目）
- Journal Title
  
  眼臨紀
  
  Volume: 5 Pages: 387-391
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] ベバシズマブ硝子体内投与併用網膜光凝固術が奏効した重症未熟児網膜症の３例2012
- Author(s)
  藤田陽子、近藤寛之（8名中7番目）
- Journal Title
  
  眼臨紀
  
  Volume: 5 Pages: 377-381
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] ベバシズマブ硝子体内投与併用網膜光凝固術が奏効した重症未熟児網膜症の3例2012
- Author(s)
  藤田陽子、近藤寛之
- Journal Title
  
  眼臨紀
  
  Volume: (5) Pages: 377-381
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] 黄斑剥離を伴う裂孔原性網膜剥離に対する硝子体術後の変視量の検討2012
- Author(s)
  森田啓文、近藤寛之
- Journal Title
  
  眼科手術
  
  Volume: (26) Pages: 449-452
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] Novel compound heterozygous mutations in the MFRP gene in a Japanese patient with posterior microphthalmos2012
- Author(s)
  Matsushita I, Kondo H　（3名中2番目）
- Journal Title
  
  Japanese Journal of Ophthalmology
  
  Volume: 56 Issue: 4 Pages: 396-400
- DOI
  10.1007/s10384-012-0145-4
- NAID
  10030952220
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] 小眼球症に伴う眼窩発育異常の画像評価2012
- Author(s)
  仁科幸子、近藤寛之
- Journal Title
  
  眼臨紀
  
  Volume: (5) Pages: 387-391
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] 黄斑剥離を伴う裂孔原性網膜剥離に対する硝子体術後の変視量の検討2012
- Author(s)
  森田啓文、近藤寛之（3名中2番目）
- Journal Title
  
  眼科手術
  
  Volume: 25 Pages: 449-452
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] National survey of microphthalmia in Japan2012
- Author(s)
  Nishina S, Kurosaka D, Nishida Y. Kondo H, et al. et al
- Journal Title
  
  Jpn J Ophthalmol
  
  Volume: (56) Pages: 198-202
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] Survey of microphthalmia in Japan.2012
- Author(s)
  Nishina S, Kurosaka D, Nishida Y, Kondo H, Kobayashi Y, Azuma N.
- Journal Title
  
  Jpn J Ophthalmol
  
  Volume: 56 Issue: 3 Pages: 198-202
- DOI
  10.1007/s10384-012-0126-7
- NAID
  10030626740
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22390327, KAKENHI-PROJECT-22591956, KAKENHI-PROJECT-22591975, KAKENHI-PROJECT-24659770
[Journal Article] Novel compound heterozygous mutations in MFRP gene in Japanese patient with posterior microphthalmos2012
- Author(s)
  Matsushita I, Kondo H, et al
- Journal Title
  
  Jpn J Ophthalmol
  
  Volume: (56) Pages: 396-400
- NAID
  10030952220
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] National survey of microphthalmia in Japan2012
- Author(s)
  Nishina S, Kurosaka D, Nishida Y.Kondo H, et al
- Journal Title
  
  Jpn J Ophthalmol
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] Transcriptional regulation of activating transcription factor 4 (ATF4) under oxidative stress in retinal pigment epithelial ARPE-19 cells2011
- Author(s)
  Miyamoto N, Izumi H, Miyamoto R, Bin H, Kondo H, et al
- Journal Title
  
  Invest Ophthalmol Vis Sci
  
  Volume: (52) Pages: 1226-34
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] Mutations in TSPAN12 gene in Japanese patients with familial exudative vitreoretinopathy2011
- Author(s)
  Kondo H, Kusaka S, Yoshinaga A, et al.
- Journal Title
  
  Am J Ophthalmol
  
  Volume: Epub ahead of print
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] 家族性滲出性硝子体網膜症(特集・遺伝性網膜・黄斑ジストロフィアップデート)2011
- Author(s)
  近藤寛之
- Journal Title
  
  あたらしい眼科
  
  Volume: (28) Pages: 963-968
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] Mutations in TSPAN12 gene in Japanese patients with familial exudative vitreoretinopathy2011
- Author(s)
  Kondo H, Kusaka S, Yoshinaga A, et al
- Journal Title
  
  Am J Ophthalmol
  
  Volume: 151 Issue: 6 Pages: 1095-1100
- DOI
  10.1016/j.ajo.2010.11.026
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] Quercetin induces the expression of peroxiredoxins 3 and 5 via the Nrf2/NRF1 transcription pathway2011
- Author(s)
  Miyamoto N, Izumi H, Miyamoto R, Kondo H, et al
- Journal Title
  
  Invest Ophthalmol Vis Sci
  
  Volume: (52) Pages: 1055-1063
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] 重症未熟児網膜症に対しベバシズマブ硝子体内投与を行った症例の検討2011
- Author(s)
  有田直子、林英之、内尾英一、近藤寛之
- Journal Title
  
  臨床眼科
  
  Volume: (65) Pages: 1225-1229
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] 未熟児網膜症に対する抗VEGF療法の効果の検討v2011
- Author(s)
  渡辺晃久、近藤寛之他
- Journal Title
  
  眼科手術
  
  Volume: (25) Pages: 115-119
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] Quercetin induces the expression of peroxiredoxins 3 and 5 via the Nrf2/NRF1 transcription pathway2011
- Author(s)
  Miyamoto N, Izumi H, Miyamoto R, Kondo H, et al.
- Journal Title
  
  Invest Ophthalmol Vis Sci
  
  Volume: 52 Pages: 1055-1063
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] Mutations in TSPAN12 gene in Japanese patients with familial exudative vitreoretinopathy2011
- Author(s)
  Kondo H, Kusaka S, Yoshinaga A, Uchio E, Tahira T
- Journal Title
  
  Am J Ophthalmol
  
  Volume: (151) Pages: 1095-1100
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] 成人と小児における増殖硝子体網膜症の手術成績2010
- Author(s)
  小山田剛、近藤寛之、林英之、内尾英一
- Journal Title
  
  臨眼
  
  Volume: (64) Pages: 543-546
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] A case of Fukuyama congenital muscular dystrophy associated with negative electroretinograms2010
- Author(s)
  Kondo H, Saito K, Urano M, et al
- Journal Title
  
  Jpn J Ophthalmol
  
  Volume: (54) Pages: 662-624
- NAID
  10027666559
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] 増殖性硝子体網膜症に対して硝子体手術を行った小児の眼限局型Stickler症候群の1例2010
- Author(s)
  日吉篤史、近藤寛之、原潤、吉田茂生、内尾英一
- Journal Title
  
  眼科手術 23
  
  Pages: 163-166
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopaty.2010
- Author(s)
  Poulter JA, Ali M, Gilmour DF, Rice A, Kondo H, et al.
- Journal Title
  
  Am J Hum Genet 86
  
  Pages: 248-252
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 眼科(4)色覚異常、(9)網膜色素変性、(12)網膜剥離. 臨床病理レビュー2010
- Author(s)
  近藤寛之
- Journal Title
  
  特集病気をもちながらどこまで働けるか―疾病と就労の臨床診断―
  
  Volume: (146) 214
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] Mutations in TSPAN12 cause autosomal-dominant familial exsudative vitreoretinopaty2010
- Author(s)
  Poulter JA, Ali M, Gilmour DF, Rice A, Kondo H, et al.
- Journal Title
  
  Am J Hum Genet 86
  
  Pages: 248-252
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 眼科(4)色覚異常、(9)網膜色素変性、(12)網膜剥離2010
- Author(s)
  近藤寛之
- Journal Title
  
  臨床病理レビュー、特集病気をもちながらどこまで働けるか-疾病と就労の臨床診断-
  
  Volume: 146
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] A case of Fukuyama congenital muscular dystrophy associated with negative electroretinograms2010
- Author(s)
  Kondo H, Saito K, Urano M, et al.
- Journal Title
  
  Jpn J Ophthalmol
  
  Volume: 54 Pages: 622-624
- NAID
  10027666559
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] 成人と小児における増殖硝子体網膜症の手術成績2010
- Author(s)
  小山田剛、近藤寛之、林英之、内尾英一
- Journal Title
  
  臨床眼科
  
  Volume: 64 Pages: 543-546
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591956
[Journal Article] 特集未熟児網膜症診療の最前線硝子体手術の功罪2009
- Author(s)
  近藤寛之
- Journal Title
  
  臨床眼科 63
  
  Pages: 152-158
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 壮年期発症の眼底所見が軽微な錐体杆体ジストロフィの1例2009
- Author(s)
  原潤、近藤寛之、林英之、内尾英一、藤原恵理子、林研
- Journal Title
  
  臨眼 63
  
  Pages: 1155-1158
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Aggressive posterior retinopathy of prematurityの臨床経過と治療成績2009
- Author(s)
  有田直子、近藤寛之、林英之、内尾英一
- Journal Title
  
  臨眼 63
  
  Pages: 1081-1085
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 家族性滲出性硝子体網膜症2009
- Author(s)
  近藤寛之
- Journal Title
  
  眼臨紀 2
  
  Pages: 351-356
- NAID
  10024807294
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 未熟児網膜症に対する私の考え方-基礎研究から-2009
- Author(s)
  近藤寛之
- Journal Title
  
  眼科臨床紀要 2
  
  Pages: 11-15
- NAID
  10024806657
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Lens-sparing vitrectomy effective for reattachment of newly developed falciform retinal detachment in a patient with Norrie disease.2009
- Author(s)
  Shima C, Kusaka S, Kondo H, Hasebe H, Fujikado T, Tano Y
- Journal Title
  
  Arch Ophthalmol 127
  
  Pages: 579-580
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 家族性滲出性硝子体網膜症(小児眼科学会講習会「小児網膜疾患の病態・治療」)2009
- Author(s)
  近藤寛之
- Journal Title
  
  眼科臨床紀要 2
  
  Pages: 351-356
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 光凝固の適応と病期分類(特集未熟児網膜症診療-最近の考え方)2009
- Author(s)
  近藤寛之
- Journal Title
  
  あたらしい眼科 26
  
  Pages: 449-453
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Late recurrence of retinal detachment following successful vitreous surgery for stages 4B and 5 retinopathy of prematurity2009
- Author(s)
  Kondo H, Arita N, Osato M, Hayashi H, et al.
- Journal Title
  
  Am J Ophthalmol 147
  
  Pages: 661-666
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Novel mutation in PAX3 gene in Waardenburg syndrome accompanied by unilateral macular degeneration2009
- Author(s)
  Kozawa M, Kondo H, Tahira T, et al.
- Journal Title
  
  Eye 23
  
  Pages: 1619-1621
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Stickler症候群が疑われた小児の裂孔原性網膜剥離の1例2009
- Author(s)
  北崎理沙、右田博敬、有田直子、近藤寛之、内尾英一
- Journal Title
  
  眼臨紀 2
  
  Pages: 835-837
- NAID
  10025557217
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Late recurrence of retinal detachment following successful vitreous surgery for stages 4B and 5 retinopathy of prematurity.2009
- Author(s)
  Kondo H, Arita N, Ohsato M, Hayashi H, Uchio E, Oshima K
- Journal Title
  
  Am J Ophthalmol 147
  
  Pages: 661-666
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Lens-sparing vitrectomy effective for reattachment of newly developed falciform retinal detachment in a patient with Norrie disease2009
- Author(s)
  Shima C, Kusaka S, Kondo H, et al.
- Journal Title
  
  Arch Ophthalmol 127
  
  Pages: 579-580
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Novel mutation in PAX3 gene in Waardenburg syndrome accompanied by unilateral macular degeneration.2009
- Author(s)
  Kozawa M, Kondo H, Tahira T, Hayashi K, Uchio E
- Journal Title
  
  Eye 23
  
  Pages: 1619-1621
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 網膜硝子体診療update IV. 注目の疾患その他・黄斑ジストロフィ2009
- Author(s)
  近藤寛之
- Journal Title
  
  臨床眼科 62
  
  Pages: 374-382
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 家族性惨出性硝子体網膜症の原因遺伝子の骨密度への影響2008
- Author(s)
  中森玄司, 近藤寛之, 内尾英一
- Journal Title
  
  眼科臨床紀要 1
  
  Pages: 1094-1097
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy2008
- Author(s)
  Qin M, Kondo H, Tahira T, Hayashi K
- Journal Title
  
  Hum Genet 122
  
  Pages: 615-623
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy.2008
- Author(s)
  Qin M, Kondo H, Tahira T, Hayashi K
- Journal Title
  
  Hum Genet 122
  
  Pages: 615-623
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 遺伝子診断を行ったノリエ病2家系の臨床像2008
- Author(s)
  宮河あやこ, 近藤寛之, 林英之, 他
- Journal Title
  
  眼科臨床紀要 1
  
  Pages: 453-456
- NAID
  10024295594
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 特集網膜病変の最近の考え方と新しい知見家族性滲出性硝子体網膜症2008
- Author(s)
  近藤寛之
- Journal Title
  
  臨床眼科 62
  
  Pages: 138-144
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 生後4週目に光凝固を行った色素失調症の1例2007
- Author(s)
  淵上あき, 近藤寛之, 林英之, 内尾英一
- Journal Title
  
  眼科臨床医報 101
  
  Pages: 529-531
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 超低出生体重児の予後.超低出生体重児における未熟児網膜症の視覚予後2007
- Author(s)
  近藤寛之
- Journal Title
  
  周産期医学 37
  
  Pages: 501-506
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 小児眼科に役立つ遺伝子診断・遺伝的異質性の考え方2007
- Author(s)
  近藤寛之
- Journal Title
  
  眼科臨床医報 101
  
  Pages: 505-507
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Severe Form of Familial Exudative Vitreoretinopathy Caused by Homozygous R417Q Mutation in Frizzled-4 Gene.2007
- Author(s)
  Kondo H, Qin M, Tahira T, Uchio E, Hayashi K
- Journal Title
  
  Ophthalmic Genet 28
  
  Pages: 220-223
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] 眼科専門医に必要な全身疾患と眼のすべて.色素失調症2007
- Author(s)
  近藤寛之
- Journal Title
  
  臨床眼科 61
  
  Pages: 286-289
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Severe Form of Famital Exudative Vitreoretinopathy Caused by Homozygous R417Q Mutation in Frizzled-4 Gene2007
- Author(s)
  Kondo H, Qin M, Tahira T, Uchio E, Hayashi K
- Journal Title
  
  Ophthalmic Genet 28
  
  Pages: 220-223
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19592047
[Journal Article] Prenatal development of the eye2006
- Author(s)
  H.Kondo
- Journal Title
  
  Perinatal Medicine 36-4
  
  Pages: 409-417
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] 小瞳孔を合併した家族性小眼球の1家系2006
- Author(s)
  中森玄司, 近藤寛之, 小西健一
- Journal Title
  
  日本眼科紀要 57
  
  Pages: 102-107
- NAID
  10018327579
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Novel OPA1 mutations identified in Japanese pedigrees with optic atrophy2006
- Author(s)
  M.Qin, H.Kondo, H.Uno, E.Fujiwara, E.Uchio T.Tahira, K.Hayashi
- Journal Title
  
  Mol Vis 12
  
  Pages: 485-491
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Novel OPA1 Mutations Identified in Japanese Pedigrees with Optic Atrophy2006
- Author(s)
  Qin M, Kondo H, Uno H, Hayashi K, Fujiwara E, Uchio E, Tahira T, Hayashi K
- Journal Title
  
  Mol Vis 12
  
  Pages: 485-491
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] LRP5遺伝子変異による常染色体劣性家族性滲出性硝子体網膜症2006
- Author(s)
  井上浩利, 近藤寛之, 宇野英明, 秦明輝, 林健志
- Journal Title
  
  日本学科紀要 57
  
  Pages: 139-142
- NAID
  10018327732
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] 新生児の眼科疾患「視覚器の発生」2006
- Author(s)
  近藤寛之
- Journal Title
  
  周産期医学 36
  
  Pages: 409-417
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Autosomal-recessive familial exudative vitreoretinopahty associated with LRP5 gene mutations2006
- Author(s)
  T.Inoue, H.Kondo, H.Uno, M.Qin, K.Hayashi
- Journal Title
  
  Folia Ophthalmol Jpn 57-2
  
  Pages: 139-142
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Familial microphthalmia with microcoria2006
- Author(s)
  G.Nakamori, H.Kondo, K.I.Konishi
- Journal Title
  
  Folia Ophthalmol Jpn 57-2
  
  Pages: 102-107
- NAID
  10018327579
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Genotype-phenotype correlation in familial exudative vitreoretinopathy or Norrie disease with mutations in the Norrie disease gen2006
- Author(s)
  H.Kondo, M.Qin, H.Hayashi, E.Uchio, T.Tahira, K.Hayashi
- Journal Title
  
  Invest Ophthalmol Vis Sci 47-E-4606
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes2005
- Author(s)
  Kondo H, Qin M, Hayashi H, Hayashi K, Oshima K, Tahira T, Hayashi K
- Journal Title
  
  Hum Mutal 26
  
  Pages: 104-112
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Vitreoretinal findings in families with autosomal dominant familial exudative vitreoretinopathy with or without frizzled-4 gene mutations2005
- Author(s)
  Y.Inahara, H.Kondo, K.Oshima
- Journal Title
  
  Jpn Rev Clin Ophthalmol 99-1
  
  Pages: 1-3
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] FZD4 and/or LRP5 Gene Mutations in 14 Japanese Families With Familial Exudative Vitreoretinopathy2005
- Author(s)
  H.Kondo, M.Qin, H.Hayashi, K.Oshima, T.Tahira, K.Hayashi
- Journal Title
  
  Invest Ophthalmol Vis Sci 46-E-1797
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] FZD4 and/or LRP5 Gene Mutations in 14 Jaoanese Families With Familial Exudative Vitreoretinopathy2005
- Author(s)
  Kondo H, Qin M, Hayashi H, Oshima K, Tahira T, Hayashi K
- Journal Title
  
  Invest Ophthalmol Vis Sci 46
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] A Case of Incontinentia Pigmenti in Japan : Clinical Manifestations and Genetic Examination2005
- Author(s)
  J.Y.Huang, H.Kondo, H.Hayashi, K.Oshima
- Journal Title
  
  Invest Ophthalmol Vis Sci 46-E-1799
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] 家族性滲出性硝子体網膜症の家族例の臨床所見-FZD4変異の有無による検討-2005
- Author(s)
  稲原芳生, 近藤寛之, 大島健司
- Journal Title
  
  眼科臨床医報 99
  
  Pages: 1-3
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] A Case of Incontinentia Pigmenti in Japan : Clinical Manifestations and Genetic Examination2005
- Author(s)
  Huang JY, Kondo H, Hayashi H, Oshima K
- Journal Title
  
  Invest Ophthalmol Vis Sci 46
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes2005
- Author(s)
  M.Qin, H.Hayashi, K.Oshima, T.Tahira, K.Hayashi, H.Kondo
- Journal Title
  
  Hum Mutat 26-2
  
  Pages: 104-112
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Complexity of the phenotype-genotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes2005
- Author(s)
  Qin M, Hayashi H, Oshima K, Tahira T, Hayashi K, Kondo
- Journal Title
  
  Hum Mutat 26・2
  
  Pages: 104-112
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Search for mulations in patients with autosomal recessive retinitis pigmentosa using homozygosity-based screening with multiple locus?specific microsatellite markers2004
- Author(s)
  Kondo H, Qin M, Mizota A, Kondo M, Hayashi H, Hayashi K, Oshima K, Tahira T, Hayashi K
- Journal Title
  
  Invest Ophthalmol Vis Sci 45
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] 第一次硝子体過形成遺残と診断されていた家族性滲出性硝子体網膜症の一家系2004
- Author(s)
  宇野英明, 近藤寛之, 桧垣卓夫, 大島健司
- Journal Title
  
  眼科臨床医報 98
  
  Pages: 7-9
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] A family that was first diagnosed with persistent hyperplastic primary vitreous and later rediagnosed as familial exudative vitreoretinopathy2004
- Author(s)
  H.Uno, H.Kondo, H.T., K.Oshima
- Journal Title
  
  Jpn Rev Clin Ophthalmol 98-9
  
  Pages: 7-9
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa, using microsatellite markers2004
- Author(s)
  Kondo H, Qin M, Mizota A, Kondo M, Hayashi H, Hayashi K, et al.
- Journal Title
  
  Invest Ophthalmol Vis Sci 45
  
  Pages: 4433-4439
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Search for mutations in patients with autosomal recessive retinitis pigmentosa using homozygosity-based screening with multiple locus-specific micro satellite markers2004
- Author(s)
  H.Kondo, M.Qin, A.Mizota, M.Kondo, H.Hayashi, K.Oshima, T.Tahira, K.Hayashi
- Journal Title
  
  Invest Ophthalmol Vis Sci 45-E-5091
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa using mirosatellite markers2004
- Author(s)
  H.Kondo, M.Qin, A.Mizota, M.Kondo, H.Hayashi, K.Hayashi, K.Oshima, T.Tahira, K.Hayashi
- Journal Title
  
  Invest Ophthalmol Vis Sci 45-12
  
  Pages: 4433-4439
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentose using microsatellite markers2004
- Author(s)
  Kondo H, Qin M, Mizota A, Kondo M, Hayashi H, Hayashi K, Oshima K, Tahira T, Hayashi K
- Journal Title
  
  Invest Ophthalmol Vis Sci 45
  
  Pages: 4433-4439
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Homozygosity-based screening with multiple locus-specific microsatellite markers toward the diagnosis of autosomal recessive retinitis pigmentosa2003
- Author(s)
  H.Kondo, T.Tahira, A.Mizota, M.Kondo, H.Hayashi, K.Hayashi
- Journal Title
  
  Am J Hum Genet 73(suppl)-s578
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Frizzled 4 gene(FZD4)mutations in patients with familial exudative vitreoretinopathy with variable expressivity2003
- Author(s)
  H.Kondo, H.Hayashi, K.Oshima, T.Tahira, K.Hayashi
- Journal Title
  
  Br J Ophthalmol 87-10
  
  Pages: 1291-1295
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Homozygosity-based screening with multiple locus-specific microsatellite markerstoward the diagnosis of autosomal recessive retinitis pigmentose2003
- Author(s)
  Kondo H, Qin M, Mizota A, Kondo M, Hayashi H, Hayashi K, Oshima K, Tahira T, Hayashi K
- Journal Title
  
  Am J Hum Genet 73
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Frizzled 4 gene (FZD4) mutations in patients with familial exudative vitreoretinopathy with variable expressivity2003
- Author(s)
  Kondo H, Hayashi H, Oshima K, Tahira T, Hayashi K
- Journal Title
  
  Br J Ophthalmol 87
  
  Pages: 1291-1295
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Novel OPAl mutations identified in Japanese pedigrees with optic atrophy
- Author(s)
  Qin M, Kondo H, Uno H, Fujiwara E, Uchio E, Tahira T, Hayashi K
- Journal Title
  
  Mol Vis (in press)
- Data Source
  KAKENHI-PROJECT-15591883
[Journal Article] Complexity of the phenotype-genotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes
- Author(s)
  Qin M, Hayashi H, Oshima K, Tahira T, Hayashi K, Kondo H
- Journal Title
  
  Hum Mutat (in press)
- Data Source
  KAKENHI-PROJECT-15591883
[Presentation] 4連発現プラスミドを用いた家族性滲出性硝子体網膜症原因遺伝子の機能解析2024
- Author(s)
  奥一真、和泉弘人、近藤寛之
- Organizer
  第128回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-23K09053
[Presentation] 本邦における杆体一色覚の遺伝的病因と臨床的特徴2023
- Author(s)
  井岡大河，林孝彰，慈溝渕圭，角田和繁，國吉一樹，近藤寛之，太田淳也，小南太郎，西口康二，上野真治
- Organizer
  第70回日本臨床視覚電気生理学会
- Data Source
  KAKENHI-PROJECT-22K09825
[Presentation] PAX6遺伝子異常を伴わない孤立性黄斑低形成の検討2023
- Author(s)
  松下五佳、林孝彰、近藤寛之
- Organizer
  第127回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-20K09818
[Presentation] Stickler症候群の１家系2023
- Author(s)
  堂本綾、國吉一樹、近藤寛之、松下五佳、飯森宏仁、江浦真理子、日下俊次
- Organizer
  第77回日本臨床眼科学会
- Data Source
  KAKENHI-PROJECT-22K09825
[Presentation] 日本人におけるABCA4関連網膜ジストロフィの臨床像および遺伝的特徴に関する全国コホート研究2023
- Author(s)
  溝渕圭，林孝彰，田中公二，國吉一樹，村上祐介，中村奈津子，角田和繁，溝田淳，前田亜希子，鳥居薫子，小南太郎，上野真治，西口康二，池田康博，近藤峰生，堀田喜裕，中野匡
- Organizer
  第62回日本網膜硝子体学会総会
- Data Source
  KAKENHI-PROJECT-22K09825
[Presentation] 乳幼児家族性滲出性硝子体網膜症の両親の超広角蛍光眼底造影スコアと遺伝子解析2022
- Author(s)
  岡本美里、永田竜朗、松下五佳、近藤寛之
- Organizer
  第76回日本網膜硝子体学会総会
- Data Source
  KAKENHI-PROJECT-20K09818
[Presentation] PAX6標的遺伝子の検索と孤立性黄斑低形成例における関与2022
- Author(s)
  松下五佳、和泉弘人、近藤寛之
- Organizer
  第126回日本眼科学会
- Data Source
  KAKENHI-PROJECT-20K09818
[Presentation] 我が国の家族性滲出性硝子体網膜症250家系の遺伝子解析2022
- Author(s)
  近藤寛之、松下五佳、川村朋子、内尾英一、日下俊次、林孝彰、白澤誠、仁科幸子、金子優、川崎良、坂本泰二
- Organizer
  第126回日本眼科学会
- Data Source
  KAKENHI-PROJECT-20K09818
[Presentation] COL2A1ミスセンス変異に黄斑変性を合併したSticklerr症候群の2家系2021
- Author(s)
  浅野真美加、奥一真、横山勝彦、木許賢一、久保田敏昭、近藤寛之
- Organizer
  日本人類遺伝学会第6大会第28回日本遺伝子診療学会大会
- Data Source
  KAKENHI-PROJECT-20K09818
[Presentation] マルチカラー走査レーザー眼底カメラを用いた反射法による黄斑色素密度の測定2021
- Author(s)
  森田啓文、松下五佳、笹野紘之、尾花明、近藤寛之
- Organizer
  第75回日本臨床眼科学会
- Data Source
  KAKENHI-PROJECT-20K09818
[Presentation] 眼底疾患、白色瞳孔・瞳孔領白濁の発見と対処（教育セミナー4）2021
- Author(s)
  近藤寛之
- Organizer
  第125回日本眼科学会総会
- Invited
- Data Source
  KAKENHI-PROJECT-20K09818
[Presentation] PAX6遺伝子異常による転写機能の解析2021
- Author(s)
  松下五佳森田啓文和泉弘人近藤寛之
- Organizer
  第125回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-20K09818
[Presentation] PAX6遺伝子異常を伴う優性遺伝性孤立性黄斑低形成における臨床的特徴と遺伝子型との関連2020
- Author(s)
  松下五佳森田啓文黒田由賀利上野真治藤波芳角田和繁岩田岳寺崎浩子木内良明近藤寛之
- Organizer
  第124回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-20K09818
[Presentation] 小児眼底疾患の病態生理（特別講演）2020
- Author(s)
  近藤寛之
- Organizer
  第45回日本小児眼科学会総会
- Invited
- Data Source
  KAKENHI-PROJECT-20K09818
[Presentation] COL2A1遺伝子変異陽性のStickler症候群の網膜電位図所見2019
- Author(s)
  冨士本一志、永田竜朗、松下五佳、林孝彰、久保田敏昭、大路正人、日下俊次、近藤寛之
- Organizer
  第123回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] インストラクションコース「網膜硝子体ジストロフィの診療の実際」2019
- Author(s)
  近藤寛之、近藤峰生、林孝彰、髙橋政代、堀田喜裕
- Organizer
  第73回日本臨床眼科学会
- Invited
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] Diagnosis and management of Stickler syndrome2019
- Author(s)
  Kondo Hiroyuki
- Organizer
  Vitreoretinal Society India 2019
- Invited
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] Stickler syndrome: multimodal imaging and functional assessments2019
- Author(s)
  Kondo Hiroyuki
- Organizer
  The 60th annual meeting of the Ophthalmological Society of Taiwan, Retina symposium (I), Master course in pediatric retina
- Invited
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] Management of Stickler syndrome: Diagnosis, surgery and prophylaxis (Instruction course 34, Advances in the management of complex pediatric retinal diseases)2019
- Author(s)
  Kondo Hiroyuki
- Organizer
  19th Euretina congress Paris
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] Stickler症候群における傍血管網膜変性部の視機能2018
- Author(s)
  冨士本一志永田竜朗松下五佳林孝彰日下俊次近藤寛之
- Organizer
  第122回日本眼科学会
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] Molecular Analysis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing2018
- Author(s)
  Hosono K, Nishina S, Yokoi T, Katagiri S, Saitsu H, Kurata K, Miyamichi D, Hikoya　A, Mizobuchi K, Nakano T, Minoshima S, Fukami M, Kondo H, Sato M, Hayashi T, Azuma N, Hotta Y
- Organizer
  日本人類遺伝学会第63回大会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] 網膜から探る全身疾患のメカニズム．全身疾患と網膜変性2018
- Author(s)
  近藤寛之
- Organizer
  第122回日本眼科学会
- Invited
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] 7歳時に診断されたStickler症候群の女児2018
- Author(s)
  林孝彰久保朗子溝渕圭片桐聡大熊康弘近藤寛之中野匡
- Organizer
  第43回日本小児眼科学会講習会
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] Mutation Analysis of Japanese Patients with Leber Congenital Amaurosis by Next Generation Sequencing2018
- Author(s)
  Hosono K, Nishina S, Yokoi T, Katagiri S, Kurata K, Miyamichi D, Mizobuchi K, Nakano T, Minoshima S, Fukami M, Kondo H, Sato M, Hayashi T, Azuma N, Hotta Y
- Organizer
  ARVO2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] Foveal hypoplasia in patients with Stickler syndrome2018
- Author(s)
  Kondo Hiroyuki
- Organizer
  Association of Pediatric Retinal Surgeons Meeting
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] 日本人Leber先天盲の次世代シークエンサーによる遺伝子変異解析2018
- Author(s)
  細野克博、仁科幸子、林孝彰、倉田健太郎、横井匡、片桐聡、宮道大督、溝渕圭、佐藤美保、蓑島伸生、深見真紀、中野匡、近藤寛之、東範行、堀田喜裕
- Organizer
  第122回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] 小児網膜変性疾患の病態と診断　網膜硝子体変性2018
- Author(s)
  近藤寛之
- Organizer
  第72回日本臨床眼科学会
- Invited
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] Foveal hypoplasia in patients with Stickler syndrome2018
- Author(s)
  Kondo Hiroyuki
- Organizer
  3rd International Pediatric Vitreoretinal Summit Forum
- Invited
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] 遺伝性網脈絡膜変性疾患　-遺伝子検査、網膜検査への対応　インストラクションコース2018
- Author(s)
  堀田喜裕、近藤寛之、近藤峰生、高橋政代、林孝彰
- Organizer
  第72回日本臨床眼科学会
- Data Source
  KAKENHI-PROJECT-17K11447
[Presentation] Foveal hypoplasia in patients with Stickler syndrome2017
- Author(s)
  Kondo, H
- Organizer
  2017 Taiwan Macula Society Annal Meeting
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] Stickler症候群に見られる網膜傍血管変性の眼底自発蛍光所見2017
- Author(s)
  冨士本一志, 永田竜朗, 松下五佳, 林孝彰, 久保田敏昭, 大路正人, 日下俊次, 近藤寛之
- Organizer
  第121回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] 黄斑反射消失を契機に診断されたStickler症候群I型の１例2017
- Author(s)
  林孝彰, 片桐聡, 溝渕圭, 松下五佳, 近藤寛之
- Organizer
  第42回日本小児眼科学会総会
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] Ultrawide field fundus autofluorescence of paravenous retinal degeneration in Stickler Syndrome2017
- Author(s)
  Kondo, H
- Organizer
  2017 Taiwan Macula Society Annal Meeting
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] Stickler症候群のマルチモダルイメージング2017
- Author(s)
  近藤寛之
- Organizer
  第19回Japan Macula Club
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] Stickler症候群のと特発性黄斑前膜の網膜硝子体境界面のOCT En face所見の比較2017
- Author(s)
  松下五佳, 近藤寛之
- Organizer
  第121回日本眼科学会総会
- Data Source
  KAKENHI-PROJECT-17K11441
[Presentation] 網膜分離症の遺伝型と臨床型　シンポジウム20.遺伝性網脈絡膜疾患の遺伝型と臨床型2016
- Author(s)
  近藤寛之
- Organizer
  第120回日本眼科学会総会
- Place of Presentation
  東北大学百周年記念会館（宮城県・仙台市）
- Year and Date
  2016-04-07
- Invited
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] 未熟児網膜症　シンポジウム13.小児眼科診療の今日の基準と将来の展望2016
- Author(s)
  近藤寛之
- Organizer
  第120回日本眼科学会総会
- Place of Presentation
  仙台国際センター（宮城県・仙台市）
- Year and Date
  2016-04-07
- Invited
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] Phenotypic diversity of FEVR with mutations in KIF11 gene2016
- Author(s)
  Kondo H.
- Organizer
  Association of Pediatric Retinal Surgeons Meeting
- Place of Presentation
  Cabo San Lucas, Mexico
- Year and Date
  2016-03-30
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] Mutations in ATOH7 gene in patients with congenital retinal detachment and familial exudative vitreoretinopathy2015
- Author(s)
  Kondo H., Matsushita I., Tahira T., Uchio E., Kusaka S.
- Organizer
  Annual meeting of the Association for Research in Vision and Ophthalmology
- Place of Presentation
  Colorad Convention Center, Denver, Colorad
- Year and Date
  2015-05-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] Novel mutations in KIF11 gene in Japanese patients with FEVR and MLCRD2015
- Author(s)
  Kondo H.
- Organizer
  Meeting of the international society of genetic eye disease & retinoblastoma ISGEDR
- Place of Presentation
  Faculty of Medicine's auditoriums, Dalhousie University, Halifax, Nova Scotia, Canada
- Year and Date
  2015-08-05
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] 遺伝性網膜硝子体疾患のトータルケア2015
- Author(s)
  近藤寛之
- Organizer
  第６８回日本臨床眼科学会
- Place of Presentation
  名古屋国際会議場（愛知県・名古屋市）
- Year and Date
  2015-10-22
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] Mutations in ATOH7 gene in patients with congenital retinal detachment and familial exudative vitreoretinopathy2015
- Author(s)
  H.Kondo, I. Matsushita, T. Tahira, E. Uchio, S. Kusaka
- Organizer
  Annual meeting of the Association for Research in Vision and Ophthalmology
- Place of Presentation
  Denver (U.S.A)
- Year and Date
  2015-05-05
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] 家族性滲出性硝子体網膜症2014
- Author(s)
  近藤寛之
- Organizer
  第８４回九州眼科学会
- Place of Presentation
  久留米大学筑水会館（福岡県久留米市）
- Year and Date
  2014-06-28
- Invited
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] 小児眼科疾患のフォローのコツ2014
- Author(s)
  近藤寛之
- Organizer
  第114回九州医師会総会医学会眼科分科会
- Place of Presentation
  全労済ソレイユ(大分県大分市）
- Year and Date
  2014-11-23
- Invited
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] 遺伝子診断のための検査法の実際（シンポジウム１遺伝性網膜疾患、最新のgenotyping）2014
- Author(s)
  近藤寛之
- Organizer
  第62回日本臨床視覚電気生理学会
- Place of Presentation
  両国KCFビル（東京都文京区）
- Year and Date
  2014-10-03
- Invited
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] Occurrence of retinal detachment in Japanese patients with Stickler syndrome2013
- Author(s)
  Kondo, H, Hayashi, T, Kondo, M, Ohji, M, Kusaka, S
- Organizer
  Annual meeting of the American Academy of Ophthalmology
- Place of Presentation
  New Orleans, Luisiana, USA
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] 教育講演　網膜疾患の苦手克服　遺伝性網膜疾患の説明2013
- Author(s)
  近藤寛之
- Organizer
  The 8th Asica Pacific vitreo-retina society / 第52回日本網膜硝子体学会
- Place of Presentation
  名古屋国際会議場
- Invited
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] Recent advances in genetics of pediatric retinal detachment2013
- Author(s)
  Kondo, H
- Organizer
  2nd Annual Meeting of Taiwan Retina Society
- Place of Presentation
  Taipei, Taiwan
- Invited
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] 先天小瞳孔の遺伝子解析2013
- Author(s)
  近藤寛之, 田平知子, 宮本直哉, 永田竜朗, 吉田茂生, 山本健, 田原昭彦
- Organizer
  第117回日本眼科学会総会
- Place of Presentation
  東京・東京国際フォーラム
- Data Source
  KAKENHI-PROJECT-25462743
[Presentation] 剥離の診断と治療、その進歩2013
- Author(s)
  近藤寛之
- Organizer
  網膜第151回宮崎県眼科医会講習会(招待講演)
- Place of Presentation
  宮崎市(ホテルスカイタワー)
- Year and Date
  2013-02-02
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] Autosomal recessive familial exudative vitreoretinopathy2012
- Author(s)
  Kondo H
- Organizer
  2nd Pediatric Retinal Vascular Disease Forum
- Place of Presentation
  Grand Hyatt on Union Square, San Francisco
- Year and Date
  2012-02-10
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 教育セミナー20未熟児網膜症の診断と治療硝子体手術2012
- Author(s)
  近藤寛之
- Organizer
  第35回日本眼科手術学会総会
- Place of Presentation
  名古屋国際会議場(名古屋)(招待講演)
- Year and Date
  2012-01-25
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] Genetic variations in advanced retinopathy of prematurity2012
- Author(s)
  Kondo H
- Organizer
  World ROP congress III
- Place of Presentation
  Intercontinental Shanghai Puxi, Shanghai, China
- Year and Date
  2012-10-16
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] VEGF levels in refractory Coats disease with or without intravitreal bevacizumab2012
- Author(s)
  Kondo H
- Organizer
  2nd Pediatric Retinal Vascular Disease Forum
- Place of Presentation
  Grand Hyatt on Union Square, San Francisco
- Year and Date
  2012-02-11
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] New mutation in GJA8 gene is associated with unique phenotype of familial microphthalmia with anomalies of iris and lens2012
- Author(s)
  Kondo H(5名中筆頭)
- Organizer
  Annual meeting of the Association for Research in Vision and Ophthalmology
- Place of Presentation
  Fort Lauderdale, Florida, USA
- Year and Date
  2012-05-07
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] Genetic variations of FDZ4 and LRP5 genes in eyes with advanced retinopathy of prematurity2012
- Author(s)
  Kondo H (6名中筆頭)
- Organizer
  第51回日本網膜硝子体学会
- Place of Presentation
  甲府市(富士屋ホテル)
- Year and Date
  2012-11-30
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] A case of atypical retinopathy of prematurity2012
- Author(s)
  Kondo H (単著)
- Organizer
  Association of Pediatric Retinal Surgeons Meeting
- Place of Presentation
  Hotel Park City, Park city, Uta, USA
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] A case of atypical retinopathy of prematurity2012
- Author(s)
  Kondo H
- Organizer
  5th Association of Pediatric Retinal Surgeons Meeting
- Place of Presentation
  Hotel Park City, Park city, Uta, USA
- Year and Date
  2012-09-21
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] Autosomal recessive familial exudative vitreoretinopathy2011
- Author(s)
  Kondo H
- Organizer
  2nd Pediatric Retinal Vascular Disease Forum
- Place of Presentation
  Grand Hyatt on Union Square, San Francisco, USA
- Year and Date
  2011-02-10
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] VEGF levels in refractory Coats disease with or without intravitreal bevacizumab2011
- Author(s)
  Kondo H
- Organizer
  2nd Pediatric Retinal Vascular Disease Forum
- Place of Presentation
  Grand Hyatt on Union Square, San Francisco, USA
- Year and Date
  2011-02-11
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] Search for SOX17 gene mutations in patients with familial exudative vitreoretinopathy2011
- Author(s)
  Kondo H, Tawara A, et al
- Organizer
  Annual meeting of the Association for Research in Vision and Ophthalmology
- Place of Presentation
  Fort Lauderdale, Florida, USA
- Year and Date
  2011-05-11
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] X連鎖性網膜分離症にみられたRSI遺伝子異常と臨床像2011
- Author(s)
  近藤寛之, 他
- Organizer
  第115回日本眼科学会総会
- Place of Presentation
  東京国際フォーラム(東京)
- Year and Date
  2011-05-13
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 眼科診療に必要な遺伝性網膜硝子体疾患-診療スタンダード2011-(インストラクションコース7)2011
- Author(s)
  近藤寛之, 他
- Organizer
  第65回日本臨床眼科学会
- Place of Presentation
  東京国際フォーラム(東京)
- Year and Date
  2011-10-07
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] bevacizumabを用いた未熟児網膜症の治療(インストラクションコース26)2011
- Author(s)
  近藤寛之, 他
- Organizer
  第65回日本臨床眼科学会
- Place of Presentation
  東京国際フォーラム(東京)
- Year and Date
  2011-10-08
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] Search for SOX17 Gene Mutations In Patients With Familial Exudative Vitreoretinopathy2011
- Author(s)
  Kondo H, Tawara A, et al
- Organizer
  Annual meeting of the Association for Research in Vision and Ophthalmology
- Place of Presentation
  Fort Lauderdale, Florida
- Year and Date
  2011-05-01
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 小児の網膜剥離は遺伝性か?2010
- Author(s)
  近藤寛之
- Organizer
  第111回佐賀大学眼科臨床懇話会
- Place of Presentation
  佐賀市(ホテルマリターレ創世佐賀)
- Year and Date
  2010-10-16
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] わが国のStickler症候群にみられたCOL2A1遺伝子異常とその臨床像2010
- Author(s)
  近藤寛之, 他
- Organizer
  第114回日本眼科学会総会
- Place of Presentation
  名古屋(国際会議場)
- Year and Date
  2010-04-16
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 重症Coats病にみられた眼内VEGF濃度勾配とbevacizumab硝子体投与の効果2010
- Author(s)
  近藤寛之 (4名中筆頭)
- Organizer
  第66回日本臨床眼科学会
- Place of Presentation
  京都国際会議場、京都市
- Year and Date
  2010-10-25
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 遺伝性網膜疾患のトピックス～遺伝性網膜硝子体症～2010
- Author(s)
  近藤寛之
- Organizer
  第85回網膜病変談話会
- Place of Presentation
  東京都(興和大ホール)
- Year and Date
  2010-11-04
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] TSPAN12遺伝子異常による家族性滲出性硝子体網膜症2010
- Author(s)
  近藤寛之、他
- Organizer
  第64回日本臨床眼科学会
- Place of Presentation
  神戸市(ポートピアホテル)
- Year and Date
  2010-11-12
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] bevacizumabを用いた未熟児網膜症の治療(インストラクションコース26)2010
- Author(s)
  近藤寛之他
- Organizer
  第65回日本臨床眼科学会
- Place of Presentation
  東京都(東京国際フォーラム)
- Year and Date
  2010-10-08
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] わが国のStickler症候群にみられたCOL2A1遺伝子異常とその臨床像2010
- Author(s)
  近藤寛之、他
- Organizer
  第114回日本眼科学会総会
- Place of Presentation
  名古屋市(国際会議場)
- Year and Date
  2010-04-16
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 網膜剥離の診かた、治療の考え方2010
- Author(s)
  近藤寛之
- Organizer
  第48回六大学合同眼科研究会
- Place of Presentation
  隔岡(九州大学百年講堂)
- Year and Date
  2010-09-04
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 小児の網膜剥離は遺伝性か?2010
- Author(s)
  近藤寛之
- Organizer
  第111回佐賀大学眼科臨床懇話会
- Place of Presentation
  佐賀(ホテルマリターレ創世佐賀)
- Year and Date
  2010-10-16
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 網膜剥離の診かた、治療の考え方2010
- Author(s)
  近藤寛之
- Organizer
  第48回六大学合同眼科研究会
- Place of Presentation
  福岡市(九州大学百年講堂)
- Year and Date
  2010-09-04
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 遺伝性網膜疾患のトピックス～遺伝性網膜硝子体症～2010
- Author(s)
  近藤寛之
- Organizer
  第85回網膜病変談話会
- Place of Presentation
  東京(興和大ホール)
- Year and Date
  2010-11-04
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] TSPAN12遺伝子異常による家族性滲出性硝子体網膜症2010
- Author(s)
  近藤寛之, 他
- Organizer
  第64回日本臨床眼科学会
- Place of Presentation
  神戸(ポートピアホテル)
- Year and Date
  2010-11-12
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] わが国の常染色体優性家族性滲出性硝子体網膜症の遺伝子診断に基づいた浸透率.2009
- Author(s)
  近藤寛之、林健志, 他
- Organizer
  第63回日本臨床眼科学会
- Place of Presentation
  福岡
- Year and Date
  2009-10-10
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] Genetic heterogeneity in familial exudative vitreoretinopathy with reduced bone mineral density2009
- Author(s)
  Kondo H, Nakamori G, Qin M, Tahira T, Uchio E, Hayashi K
- Organizer
  ARVO Annual Meeting
- Place of Presentation
  Fort Lauderdale
- Year and Date
  2009-01-31
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] 連鎖解析的手法により新規COL2A1遺伝子異常を同定したstickler症候群の1家系2009
- Author(s)
  近藤寛之, 他
- Organizer
  第113回日本眼科学会総会
- Place of Presentation
  東京(東京国際フォーラム)
- Year and Date
  2009-04-16
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] 黄斑部疾患の硝子体手術:適応の選択2009
- Author(s)
  近藤寛之
- Organizer
  第30回産業医大研究会
- Place of Presentation
  北九州(産業医科大学)
- Year and Date
  2009-11-07
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] わが国の常染色体優性家族性滲出性硝子体網膜症の遺伝子診断に基づいた浸透率2009
- Author(s)
  近藤寛之, 他
- Organizer
  第63回日本臨床眼科学会
- Place of Presentation
  福岡(マリンメッセ福岡)
- Year and Date
  2009-10-10
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] 小児眼底疾患の診断と治療「硝子体変性症」.2009
- Author(s)
  近藤寛之
- Organizer
  第113回日本眼科学会総会
- Place of Presentation
  東京
- Year and Date
  2009-04-17
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] 福山型筋ジストロフィの重症例にみられた陰性ERG所見2009
- Author(s)
  近藤寛之, 他
- Organizer
  第57回日本臨床視覚電気生理学会
- Place of Presentation
  千葉(浦安市民プラザwave101)
- Year and Date
  2009-10-30
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] 小児・若年性網膜疾患の診断の新たな展開2009
- Author(s)
  近藤寛之
- Organizer
  第79回九州眼科学会
- Place of Presentation
  福岡(アクロス福岡)
- Year and Date
  2009-05-30
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] 小児眼底疾患の診断と治療「硝子体変性症」2009
- Author(s)
  近藤寛之
- Organizer
  第113回日本眼科学会総会
- Place of Presentation
  東京(東京国際フォーラム)
- Year and Date
  2009-04-17
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] シンポジウム10. 重症未熟児網膜症に対する初期手術選択と適応. 「硝子体手術の功罪」2008
- Author(s)
  近藤寛之
- Organizer
  第112回日本眼科学会総会
- Place of Presentation
  横浜
- Year and Date
  2008-04-18
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] Late recurrence of retinal detachment following successful vitreous surgery for stages 4B and 5 retinopathy of prematurity2008
- Author(s)
  Kondo H
- Organizer
  Association of Pediatric Retinal Surgeons Meeting
- Place of Presentation
  Duck Key, Florida
- Year and Date
  2008-04-29
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] Aggressive posterior ROPの臨床経過と治療成績2008
- Author(s)
  有田直子, 近藤寛之, 林英之, 内尾英一
- Organizer
  第62回臨床眼科学会
- Place of Presentation
  東京
- Year and Date
  2008-10-25
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] IKBKG遺伝子解析を行った色素失調症の4家系の臨床像2008
- Author(s)
  近藤寛之, ファンジェーン, 内尾英一
- Organizer
  第62回臨床眼科学会
- Place of Presentation
  東京
- Year and Date
  2008-10-25
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] Genetic heterogeneityin familial exudative vitreoretinopathywith reduced bone mineral density2008
- Author(s)
  Kondo H, Nakamori G, Qin M, Tahira T, Uchio E, Hayashi K
- Organizer
  ARVO Annual Meeting
- Place of Presentation
  Fort Lauderdale
- Year and Date
  2008-04-29
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] 小児網膜疾患の病態・治療. 1. に家族性滲出性硝子体網膜症の病態・遺伝2008
- Author(s)
  近藤寛之
- Organizer
  日本小児眼科学会講習会
- Place of Presentation
  東京
- Year and Date
  2008-07-05
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] 常染色体優性遺伝性の前眼部形成異常を伴う小眼球症に対する遺伝子解析2007
- Author(s)
  近藤寛之, 秦明輝, 田平知子, 中森玄司, 内尾英一, 林健志
- Organizer
  第61回日本臨床眼科学会
- Place of Presentation
  京都
- Year and Date
  2007-10-12
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] 家族性滲出性硝子体網膜症の遺伝子変異とWNTシグナル古典的経路の転写活性の変化2007
- Author(s)
  近藤寛之, 秦明輝, 田平知子, 内尾英一, 林健志
- Organizer
  第111回日本眼科学会総会
- Place of Presentation
  大阪
- Year and Date
  2007-04-19
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] シンポジウム:未熟児網膜症に対する私の考え方1.基礎研究から2007
- Author(s)
  近藤寛之
- Organizer
  第32回日本小児眼科学会総会
- Place of Presentation
  名古屋
- Year and Date
  2007-06-15
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] Clinical and Genetic Characteristics of a Japanese Family with Bilateral Microphathalmia, Cataract and the Absence of Pupil Formation2007
- Author(s)
  Kondo H, Qin M, Tahira T、 Uchio E, Hayashi K
- Organizer
  ARVO Annual Meeting
- Place of Presentation
  Fort Lauderdale
- Year and Date
  2007-05-07
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] 基調講演v.遺伝的背景から見た網膜疾患.2007
- Author(s)
  近藤寛之
- Organizer
  第7 7回九州眼科学会
- Place of Presentation
  宮崎
- Year and Date
  2007-05-11
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] 家族性滲出性硝子体網膜症の遺伝子変異とwntシグナル古典的経路の転写活性の変化.2007
- Author(s)
  近藤寛之, 秦明輝, 田平知子, 内尾英一, 林健志
- Organizer
  第111回日本眼科学会総会
- Place of Presentation
  大阪
- Year and Date
  2007-04-19
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] 基調講演V.遺伝的背景から見た網膜疾患2007
- Author(s)
  近藤寛之
- Organizer
  第77回九州眼科学会
- Place of Presentation
  宮崎
- Year and Date
  2007-05-11
- Data Source
  KAKENHI-PROJECT-19592047
[Presentation] 小瞳孔・白内障を伴う家族性小眼球症の原因遺伝子のエクソーム解析による同定
- Author(s)
  近藤寛之（6名中筆頭）
- Organizer
  第116回日本眼科学会総会
- Place of Presentation
  東京国際フォーラム、東京都、日本
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 未熟児網膜症最新の治療戦略
- Author(s)
  近藤寛之　(単著)
- Organizer
  第60回九州新生児研究会
- Place of Presentation
  ホテルクラウンパレス北九州、北九州市、日本
- Invited
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] Genetic variations in advanced retinopathy of prematurity
- Author(s)
  Kondo H　(単著)
- Organizer
  Association of Pediatric Retinal Surgeons Meeting
- Place of Presentation
  Hotel Park City, Park city
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] Stickler症候群など全身疾患に伴う裂孔原性網膜剥離（シンポジウム９　小児の網膜硝子体疾患）
- Author(s)
  近藤寛之　(単著)
- Organizer
  第36回日本眼科手術学会総会
- Place of Presentation
  福岡国際会議場、福岡市、日本
- Invited
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 先天小瞳孔の遺伝子解析
- Author(s)
  近藤寛之（7名中筆頭）
- Organizer
  第117回日本眼科学会総会
- Place of Presentation
  東京国際フォーラム、東京都、日本
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 真性小眼球におけるMFRP遺伝子の関与
- Author(s)
  松下五佳・近藤寛之（7名中2番目）
- Organizer
  第116回日本眼科学会総会
- Place of Presentation
  東京国際フォーラム、東京都、日本
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] Genetic variations in advanced retinopathy of prematurity
- Author(s)
  Kondo H　(単著)
- Organizer
  World ROP congress III
- Place of Presentation
  Intercontinental Shanghai Puxi, Shanghai, China
- Invited
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 重症Coats病にみられた眼内VEGF濃度勾配とbevacizumab硝子体投与の効果
- Author(s)
  近藤寛之（4名中筆頭）
- Organizer
  第６５回日本臨床眼科学会
- Place of Presentation
  京都国際会議場、京都市、日本
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] Genetic variations of FDZ4 and LRP5 genes in eyes with advanced retinopathy of prematurity
- Author(s)
  Kondo H （6名中筆頭）
- Organizer
  第51回日本網膜硝子体学会
- Place of Presentation
  富士屋ホテル, 甲府市, 日本
- Data Source
  KAKENHI-PROJECT-22591956
[Presentation] 網膜剥離の診断と治療、その進歩
- Author(s)
  近藤寛之　(単著)
- Organizer
  第151回宮崎県眼科医会講習会
- Place of Presentation
  ホテルスカイタワー、宮崎市、日本
- Invited
- Data Source
  KAKENHI-PROJECT-22591956

1. HAYASHI Kenshi (00019671)

# of Collaborated Projects: 3 results

# of Collaborated Products: 45 results
2. UTIO Eiichi (70232840)

# of Collaborated Projects: 2 results

# of Collaborated Products: 9 results
3. TAHIRA Tomoko (50155230)

# of Collaborated Projects: 2 results

# of Collaborated Products: 6 results
4. 林孝彰 (10297418)

# of Collaborated Projects: 2 results

# of Collaborated Products: 13 results
5. 和泉弘人 (50289576)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
6. TAWARA Akihiko (90117169)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. KUBOTA Toshiaki (30205140)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. YOSHIDA Shigeo (50363370)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. NAGATA Tatsuo (80389460)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. ISHIBASHI Shingo (60525442)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. Hotta Yoshihiro (90173608)

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
12. 日下俊次 (60260387)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
13. 大路正人 (90252650)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
14. 東範行 (10159395)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
15. 細野克博 (60402260)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
16. 國吉一樹 (30234470)

# of Collaborated Projects: 1 results

# of Collaborated Products: 7 results
17. 松下賢治 (40437405)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
18. 上野真治 (80528670)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
19. 落合信寿 (90386649)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
20. 扇田久和

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
21. 角田和繁

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Kondo Hiroyuki 近藤 寛之

KONDO Hiroyuki 近藤 寛之

Research Projects

Research Products

Co-Researchers

大規模医療データベースを用いた希少性網膜疾患の疫学研究に関する方法論的検討

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Genetic and molecular study for isolated familial exudative vitreoretinopathyPrincipal Investigator

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遺伝性網膜・視神経ジストロフィの症例収拾および疾患別頻度の検討

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Clinical and molecular investigation on foveal hypoplasiaPrincipal Investigator

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Clinical and genetic research for the treatment of retinal detachment in Stickler syndromePrincipal Investigator

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Construction of a comprehensive regional medical system and development of diagnostic method for rare and undiagnosed eye disease patients in Japan

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Genetic variations and functions in familial exudative vitreoretinopathyPrincipal Investigator

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Pathogenesisof Coats disease: establishing a concept of pediatric retinal detachmentPrincipal Investigator

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MOLECULAR BIOLOGICAL STUDIES IN DEVELOPMENT OF GLAUCOMA

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Genetic study for diseases of insufficient development of retinal vesselsPrincipal Investigator

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Development of a comprehensive system of linkage analysis for identification of hereditary retinal disease genes using genomic informationPrincipal Investigator

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[Book] A quick quide to pediatric retina2021

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[Book] A quick quide to pediatric retina2021

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ISBN

Kondo Hiroyuki 近藤寛之

KONDO Hiroyuki 近藤寛之

[Book] 今日の治療指針　私はこう治療している20162016

[Book] 一目でわかる眼疾患の見分け方　ぶどう膜疾患、網膜・硝子体疾患2016

[Book] Eye Surgery Now 6 きれいな小児眼科手術これであなたも悩まない!2011