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Whole exome sequencing and identification of disease phenotypes for the treatment of progressive inherited retinal disorders

Research Project

Project/Area Number 21K09756
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 56060:Ophthalmology-related
Research InstitutionJikei University School of Medicine

Principal Investigator

Hayashi Takaaki  東京慈恵会医科大学, 医学部, 教授 (10297418)

Project Period (FY) 2021-04-01 – 2024-03-31
Project Status Completed (Fiscal Year 2023)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2023: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2022: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2021: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Keywords遺伝性網膜疾患 / 黄斑ジストロフィ / 遺伝子治療 / ベータカロテン治療 / 次世代シークエンサ / 全エクソーム解析 / 視サイクル / 遺伝性網膜ジストロフィ / 網膜色素変性
Outline of Research at the Start

進行性の遺伝性網膜疾患に対する決定的な治療法は確率していない。近年、RPE65、CHM、RPGR遺伝子変異による疾患では、欧米につづき日本でも実施予定となっている。視サイクルを制御する遺伝子群(RPE65, LRAT, RDH5) の変異による疾患では9-cis-ベータカロテン治療が検討されている。原因遺伝子が特定されれば将来治療の対象となる可能性があることから、遺伝子変異を同定することは極めて重要である。本研究では、希少疾患である進行性遺伝性網膜疾患の治療実施に向け次世代シークエンサを用いた全エクソーム解析を施行し、治療に向けた基盤研究のみならず遺伝子型と疾患表現型を明らかにする。

Outline of Final Research Achievements

In inherited retinal dystrophy caused by variants in genes controlling the visual cycle (such as RPE65 and RDH5), treatment with 9-cis-beta-carotene has been reported. Therefore, we focused on RDH5-associated fundus albipunctatus (FAP), which is common in Japanese people and frequently associated with macular/cone dystrophy. We initiated a prospective study on the effect of 9-cis-beta-carotene treatment in patients with RDH5- associated FAP. We compared the amplitudes of various waveforms in electroretinograms at baseline (before treatment), three months, and one year after treatment. The results showed a statistically significant reduction in amplitude. Based on these findings, 9-cis-beta-carotene treatment for RDH5-associated FAP is not necessarily considered beneficial.

Academic Significance and Societal Importance of the Research Achievements

今回、RDH5関連白点状眼底症例の23眼に対する9-cis-ベータカロテンの1年間の治療によって、網膜電図の各種振幅が有意に低下することを明らかにした。過去の研究で、視サイクルを制御する遺伝子(RDH5など)変異による網膜ジストロフィでは、9-cis-ベータカロテン治療によって視機能が改善する症例も報告されている。RDH5関連白点状眼底において、1年の自然経過で、振幅が低下したとは考えにくく、9-cis-ベータカロテン治療は、網膜電図による評価という観点では、必ずしも有益とはならない可能性が示唆された。

Report

(4 results)
  • 2023 Annual Research Report   Final Research Report ( PDF )
  • 2022 Research-status Report
  • 2021 Research-status Report
  • Research Products

    (54 results)

All 2023 2022 2021 2020

All Journal Article (30 results) (of which Int'l Joint Research: 3 results,  Peer Reviewed: 28 results,  Open Access: 7 results) Presentation (21 results) (of which Int'l Joint Research: 5 results) Book (3 results)

  • [Journal Article] One-Year Outcomes of Oral Treatment With Alga Capsules Containing Low Levels of 9-cis-β-Carotene in RDH5-Related Fundus Albipunctatus2023

    • Author(s)
      Mizobuchi Kei、Hayashi Takaaki、Ueno Shinji、Kondo Mineo、Terasaki Hiroko、Aoki Takuya、Nakano Tadashi
    • Journal Title

      American Journal of Ophthalmology

      Volume: 254 Pages: 193-202

    • DOI

      10.1016/j.ajo.2023.06.013

    • Related Report
      2023 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] The Structural Abnormalities Are Deeply Involved in the Cause of RPGRIP1-Related Retinal Dystrophy in Japanese Patients.2023

    • Author(s)
      Torii K, Nishina S, Morikawa H, Mizobuchi K, Takayama M, Tachibana N, Kurata K, Hikoya A, Sato M, Nakano T, Fukami M, Azuma N, Hayashi T, Saitsu H, Hotta Y.
    • Journal Title

      Int J Mol Sci

      Volume: 24 Issue: 18 Pages: 13678-13678

    • DOI

      10.3390/ijms241813678

    • Related Report
      2023 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Functional Characteristics of Diverse PAX6 Mutations Associated with Isolated Foveal Hypoplasia2023

    • Author(s)
      Matsushita Itsuka、Izumi Hiroto、Ueno Shinji、Hayashi Takaaki、Fujinami Kaoru、Tsunoda Kazushige、Iwata Takeshi、Kiuchi Yoshiaki、Kondo Hiroyuki
    • Journal Title

      Genes

      Volume: 14 Issue: 7 Pages: 1483-1483

    • DOI

      10.3390/genes14071483

    • Related Report
      2023 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] A novel stop-gain <i>NF1</i> variant in neurofibromatosis type 1 and bilateral optic atrophy without optic gliomas2023

    • Author(s)
      Fukunaga Naoko、Hayashi Takaaki、Yamada Yuki、Mizobuchi Kei、Ohta Arihito、Nakano Tadashi
    • Journal Title

      Ophthalmic Genetics

      Volume: 45 Issue: 2 Pages: 186-192

    • DOI

      10.1080/13816810.2023.2245464

    • Related Report
      2023 Annual Research Report
    • Peer Reviewed
  • [Journal Article] A mild form of POC1B-associated retinal dystrophy with relatively preserved cone system function2023

    • Author(s)
      Hayashi Takaaki、Mizobuchi Kei、Kameya Shuhei、Ueno Shinji、Matsuura Tomokazu、Nakano Tadashi
    • Journal Title

      Documenta Ophthalmologica

      Volume: 147 Issue: 1 Pages: 59-70

    • DOI

      10.1007/s10633-023-09936-9

    • Related Report
      2023 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Electroretinographic abnormalities in Alport syndrome with a novel COL4A5 truncated variant (p.Try20GlyfsTer19)2023

    • Author(s)
      Mizobuchi Kei、Hayashi Takaaki、Ohira Ryo、Nakano Tadashi
    • Journal Title

      Documenta Ophthalmologica

      Volume: 146 Issue: 3 Pages: 281-291

    • DOI

      10.1007/s10633-023-09935-w

    • Related Report
      2023 Annual Research Report
    • Peer Reviewed
  • [Journal Article] 日本人enhanced S-cone syndromeの臨床的および遺伝学的特徴2022

    • Author(s)
      林孝彰、溝渕圭、亀谷修平、國吉一樹、日下俊次、上野真治、西口康二、三宅養三、中野匡
    • Journal Title

      日本眼科学会雑誌

      Volume: 126 Pages: 7-18

    • Related Report
      2022 Research-status Report 2021 Research-status Report
    • Peer Reviewed
  • [Journal Article] OPA1遺伝子に新規de novo変異が見出された両眼視神経萎縮の男児例2022

    • Author(s)
      林孝彰、溝渕圭、亀谷修平、吉田正樹、中野匡
    • Journal Title

      日本眼科学会雑誌

      Volume: 126 Pages: 983-990

    • Related Report
      2022 Research-status Report
    • Peer Reviewed
  • [Journal Article] 黄色斑眼底に類似したパターンジストロフィの1例2022

    • Author(s)
      齊藤友香、林孝彰、溝渕圭、田中公二、郡司久人、中野匡
    • Journal Title

      日本眼科学会雑誌

      Volume: 126 Pages: 588-595

    • Related Report
      2022 Research-status Report
    • Peer Reviewed
  • [Journal Article] The second Japanese family with Malattia Leventinese/Doyne honeycomb retinal dystrophy2022

    • Author(s)
      Enomoto Nobuko、Hayashi Takaaki、Matsuura Tomokazu、Tanaka Koji、Takeuchi Remi、Tomita Goji、Mori Ryusaburo
    • Journal Title

      Documenta Ophthalmologica

      Volume: 144 Issue: 1 Pages: 67-75

    • DOI

      10.1007/s10633-021-09859-3

    • Related Report
      2022 Research-status Report
    • Peer Reviewed
  • [Journal Article] Clinical characterization of autosomal dominant retinitis pigmentosa with NRL mutation in a three-generation Japanese family2022

    • Author(s)
      Mizobuchi Kei、Hayashi Takaaki、Matsuura Tomokazu、Nakano Tadashi
    • Journal Title

      Documenta Ophthalmologica

      Volume: 144 Issue: 3 Pages: 227-235

    • DOI

      10.1007/s10633-022-09874-y

    • Related Report
      2022 Research-status Report
    • Peer Reviewed
  • [Journal Article] Polypoidal choroidal vasculopathy in a patient with DMPK-associated myotonic dystrophy2022

    • Author(s)
      Iida Yuka、Hayashi Takaaki、Tokuhisa Teruaki、Mizobuchi Kei、Omoto Shusaku、Nakano Tadashi
    • Journal Title

      Documenta Ophthalmologica

      Volume: 144 Issue: 3 Pages: 217-226

    • DOI

      10.1007/s10633-022-09867-x

    • Related Report
      2022 Research-status Report
    • Peer Reviewed
  • [Journal Article] Case Report: Improved Choroidal Circulation in a Patient with Unilateral Acute Idiopathic Maculopathy2022

    • Author(s)
      Sotozono Akiko、Mizobuchi Kei、Hayashi Takaaki、Shikauchi Mamiko、Nakano Tadashi
    • Journal Title

      Optometry and Vision Science

      Volume: 99 Issue: 9 Pages: 730-734

    • DOI

      10.1097/opx.0000000000001931

    • Related Report
      2022 Research-status Report
    • Peer Reviewed
  • [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

    • Related Report
      2022 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Bardet?Biedl syndrome associated with novel compound heterozygous variants in BBS12 gene2022

    • Author(s)
      Morohashi Tamaki、Hayashi Takaaki、Mizobuchi Kei、Nakano Tadashi、Morioka Ichiro
    • Journal Title

      Documenta Ophthalmologica

      Volume: 146 Issue: 2 Pages: 165-171

    • DOI

      10.1007/s10633-022-09915-6

    • Related Report
      2022 Research-status Report
    • Peer Reviewed
  • [Journal Article] 日本人症例におけるRP1関連網膜ジストロフィの遺伝子型と表現型に関する最新の知見2022

    • Author(s)
      溝渕 圭 , 林 孝彰 , 中野 匡
    • Journal Title

      東京慈恵会医科大学雑誌

      Volume: 137 Pages: 15-26

    • Related Report
      2022 Research-status Report
    • Peer Reviewed
  • [Journal Article] 【指定難病と医療費助成】黄斑ジストロフィ2022

    • Author(s)
      林 孝彰
    • Journal Title

      あたらしい眼科

      Volume: 39 Pages: 1595-1604

    • Related Report
      2022 Research-status Report
    • Int'l Joint Research
  • [Journal Article] Clinical findings in eyes with BEST1-related retinopathy complicated by choroidal neovascularization2021

    • Author(s)
      Miyagi Mai、Takeuchi Jun、Koyanagi Yoshito、Mizobuchi Kei、Hayashi Takaaki、Ito Yasuki、Terasaki Hiroko、Nishiguchi Koji M.、Ueno Shinji
    • Journal Title

      Graefe's Archive for Clinical and Experimental Ophthalmology

      Volume: 260 Issue: 4 Pages: 1125-1137

    • DOI

      10.1007/s00417-021-05447-y

    • Related Report
      2022 Research-status Report
    • Peer Reviewed
  • [Journal Article] Novel biallelic TRPM1 variants in an elderly patient with complete congenital stationary night blindness2021

    • Author(s)
      Hayashi Takaaki、Mizobuchi Kei、Kikuchi Shinsuke、Nakano Tadashi
    • Journal Title

      Documenta Ophthalmologica

      Volume: 142 Issue: 2 Pages: 265-273

    • DOI

      10.1007/s10633-020-09798-5

    • Related Report
      2021 Research-status Report
    • Peer Reviewed
  • [Journal Article] The first Japanese family of <i>CDH3</i> ‐related hypotrichosis with juvenile macular dystrophy2021

    • Author(s)
      Hayashi Takaaki、Katagiri Satoshi、Kubota Daiki、Mizobuchi Kei、Ishiuji Yozo、Asahina Akihiko、Kameya Shuhei、Nakano Tadashi
    • Journal Title

      Molecular Genetics &amp; Genomic Medicine

      Volume: 9 Issue: 6

    • DOI

      10.1002/mgg3.1688

    • Related Report
      2021 Research-status Report
    • Peer Reviewed
  • [Journal Article] A new PDE6A missense variant p.Arg544Gln in rod?cone dystrophy2021

    • Author(s)
      Hayashi Takaaki、Mizobuchi Kei、Kameya Shuhei、Yoshitake Kazutoshi、Iwata Takeshi、Nakano Tadashi
    • Journal Title

      Documenta Ophthalmologica

      Volume: online ahead Issue: 1 Pages: 107-114

    • DOI

      10.1007/s10633-021-09826-y

    • Related Report
      2021 Research-status Report
    • Peer Reviewed
  • [Journal Article] Complete congenital stationary night blindness associated with a novel <i>NYX</i> variant (p.Asn216Lys) in middle-aged and older adult patients2021

    • Author(s)
      Hayashi Takaaki、Murakami Yusuke、Mizobuchi Kei、Koyanagi Yoshito、Sonoda Koh-Hei、Nakano Tadashi
    • Journal Title

      Ophthalmic Genetics

      Volume: 42 Issue: 4 Pages: 412-419

    • DOI

      10.1080/13816810.2021.1904422

    • Related Report
      2021 Research-status Report
    • Peer Reviewed
  • [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

    • Related Report
      2021 Research-status Report
    • Peer Reviewed
  • [Journal Article] New variants and in silico analyses in GRK1 associated Oguchi disease2021

    • Author(s)
      Poulter James A.、Gravett Molly S. C.、Taylor Rachel L.、Fujinami Kaoru、(Hayashi Takaaki) et al、UK Inherited Retinal Disease Consortium, Genomics England Research Consortium
    • Journal Title

      Human Mutation

      Volume: 42 Issue: 2 Pages: 164-176

    • DOI

      10.1002/humu.24140

    • Related Report
      2021 Research-status Report
    • Peer Reviewed
  • [Journal Article] Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN2021

    • Author(s)
      Mizobuchi Kei、Hayashi Takaaki、Oishi Noriko、Kubota Daiki、Kameya Shuhei、Higasa Koichiro、Futami Takuma、Kondo Hiroyuki、Hosono Katsuhiro、Kurata Kentaro、Hotta Yoshihiro、Yoshitake Kazutoshi、Iwata Takeshi、Matsuura Tomokazu、Nakano Tadashi
    • Journal Title

      Journal of Clinical Medicine

      Volume: 10 Issue: 11 Pages: 2265-2265

    • DOI

      10.3390/jcm10112265

    • Related Report
      2021 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Genetic and Phenotypic Landscape of PRPH2-Associated Retinal Dystrophy in Japan2021

    • Author(s)
      Oishi Akio、Fujinami Kaoru、Mawatari Go、Naoi Nobuhisa、Ikeda Yasuhiro、Ueno Shinji、Kuniyoshi Kazuki、Hayashi Takaaki、Kondo Hiroyuki、Mizota Atsushi、Shinoda Kei、Kusuhara Sentaro、Nakamura Makoto、Iwata Takeshi、Tsujikawa Akitaka、Tsunoda Kazushige
    • Journal Title

      Genes

      Volume: 12 Issue: 11 Pages: 1817-1817

    • DOI

      10.3390/genes12111817

    • Related Report
      2021 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese Patients.2021

    • Author(s)
      Murakami Y, Koyanagi Y, Fukushima M, Yoshimura M, Fujiwara K, Akiyama M, Momozawa Y, Ueno S, Terasaki H, Oishi A, Miyata M, Ikeda H, Tsujikawa A, Mizobuchi K, Hayashi T, Fujinami K, Tsunoda K, Park JY, Han J, Kim M, Lee CS, Kim SJ, Park TK, Joo K, Woo SJ, Ikeda Y, Sonoda KH.
    • Journal Title

      Ophthalmol Retina

      Volume: - Issue: 12 Pages: 1269-1279

    • DOI

      10.1016/j.oret.2021.02.009

    • Related Report
      2021 Research-status Report
    • Peer Reviewed / Int'l Joint Research
  • [Journal Article] Broad locations of antigenic regions for anti-TRPM1 autoantibodies in paraneoplastic retinopathy with retinal ON bipolar cell dysfunction2021

    • Author(s)
      Gyoten D, Ueno S, Okado S, Chaya T, Yasuda S, Morimoto T, Kondo M, Kimura K, Hayashi T, Leroy BP, Woo SJ, Mukai R, Joo K, Furukawa T.
    • Journal Title

      Exp Eye Res

      Volume: 212 Pages: 108770-108770

    • DOI

      10.1016/j.exer.2021.108770

    • Related Report
      2021 Research-status Report
    • Peer Reviewed / Int'l Joint Research
  • [Journal Article] 優性遺伝性視神経萎縮 「覚えておきたい神経眼科疾患」2021

    • Author(s)
      林 孝彰
    • Journal Title

      眼科

      Volume: 63 Pages: 1287-1295

    • Related Report
      2021 Research-status Report
  • [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

    • Related Report
      2021 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] Stargardt病(STGD1)に対する全エクソーム解析のABCA4遺伝子変異検出率の検討2023

    • Author(s)
      林孝彰、溝渕圭、亀谷修平、國吉一樹、堀田喜裕、岩田岳、中野匡
    • Organizer
      第127回日本眼科学会総会
    • Related Report
      2023 Annual Research Report
  • [Presentation] RDH5関連白点状眼底患者における1年間のドナリエラ治療効果の検討2023

    • Author(s)
      溝渕圭、林孝彰、上野真治、近藤峰生、寺崎浩子、中野匡.
    • Organizer
      第127回日本眼科学会総会
    • Related Report
      2023 Annual Research Report
  • [Presentation] An elderly case of butterfly-shaped pattern dystrophy2023

    • Author(s)
      Shikura R, Hayashi T, Mizobuchi K, Nakano T
    • Organizer
      60th Symposium of the International Society for Clinical Electrophysiology of Vision (Kyoto, Japan)
    • Related Report
      2022 Research-status Report
    • Int'l Joint Research
  • [Presentation] Electroretinographic abnormalities in X-linked Alport syndrome with a novel COL4A5 variant2023

    • Author(s)
      Mizobuchi K, Hayashi T, Ohira R, Nakano T
    • Organizer
      60th Symposium of the International Society for Clinical Electrophysiology of Vision (Kyoto, Japan)
    • Related Report
      2022 Research-status Report
    • Int'l Joint Research
  • [Presentation] Longitudinal clinical course of two siblings with KCNV2-associated retinopathy2023

    • Author(s)
      Sato T, Kuniyoshi K, Hayashi T, Nishiwaki H, Hatsukawa Y, Mizobuchi K, Tomemori R, Endo T, Nakano T, Kusaka S
    • Organizer
      60th Symposium of the International Society for Clinical Electrophysiology of Vision (Kyoto, Japan)
    • Related Report
      2022 Research-status Report
    • Int'l Joint Research
  • [Presentation] Electroretinograms of eyes with Stickler syndrome2023

    • Author(s)
      Nishimura S, Kondo H, Fujimoto K, Imanaga M, Oku K, Matsushita I, Nagata T, Hayashi T, Nagata T
    • Organizer
      60th Symposium of the International Society for Clinical Electrophysiology of Vision (Kyoto, Japan)
    • Related Report
      2022 Research-status Report
    • Int'l Joint Research
  • [Presentation] Percentage of testing performed and sensitivity of electrophysiological tests in the diagnosis of MEWDS: A multicenter study in Japan2023

    • Author(s)
      Kondo M, Saito W, Matsui Y, Tanaka T, Ishida S, Kuniyoshi K, Ueno S, Hayashi T, Nakano T, Hayakawa T, Tsunoda K, Keino H, Okada AA, Nakamura K, Akiyama H
    • Organizer
      60th Symposium of the International Society for Clinical Electrophysiology of Vision (Kyoto, Japan)
    • Related Report
      2022 Research-status Report
    • Int'l Joint Research
  • [Presentation] 日本人家族性ドルーゼンの4家系におけるEFEMP1変異のハプロタイプ解析2022

    • Author(s)
      林孝彰、溝渕圭、榎本暢子、細野克博、堀田喜裕、松浦知和、中野匡
    • Organizer
      第126回日本眼科学会総会
    • Related Report
      2022 Research-status Report
  • [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回日本眼科学会総会
    • Related Report
      2022 Research-status Report
  • [Presentation] NRL遺伝子変異による常染色体優性網膜色素変性の最初の日本人家系2022

    • Author(s)
      溝渕圭、林孝彰、中野匡
    • Organizer
      第126回日本眼科学会総会
    • Related Report
      2022 Research-status Report
  • [Presentation] CTNNB1遺伝子変異を有する症候性家族性滲出性硝子体網膜症の臨床像2022

    • Author(s)
      成瀬翔、岡本美里、林孝彰、細野克博、堀田喜裕、岡島道子、渡邊淳、東範行、日下俊次、近藤寛之
    • Organizer
      第126回日本眼科学会総会
    • Related Report
      2022 Research-status Report
  • [Presentation] Complex genetics of FEVR2022

    • Author(s)
      Kondo H, Matsushita I, Kawamura T, Kusaka S, Hayashi T, Shirasawa M, Nishina S, Kaneko Y, Kawasaki R, Sakamoto T, Uchio E
    • Organizer
      FUJIRETINA
    • Related Report
      2022 Research-status Report
  • [Presentation] .BBS12遺伝子変異によるBardet-Biedl症候群の1例2022

    • Author(s)
      諸橋環、清水翔一、中﨑公隆、林孝彰、森岡一朗
    • Organizer
      第57回日本小児腎臓病学会
    • Related Report
      2022 Research-status Report
  • [Presentation] 全エクソーム解析で診断された常染色体潜性ベストロフィノパチーの女児2022

    • Author(s)
      佐々木貴優、溝渕圭、村山耕一郎、篠田啓、林孝彰
    • Organizer
      第76回日本臨床眼科学会
    • Related Report
      2022 Research-status Report
  • [Presentation] S錐体のコントラスト感度低下を認めた顕性遺伝性視神経萎縮の1例2022

    • Author(s)
      福田有紀、大平亮、五十嵐若菜、奥出祥代、溝渕圭、林孝彰、中野匡
    • Organizer
      第63回日本視能矯正学会
    • Related Report
      2022 Research-status Report
  • [Presentation] 蝶形パターンジストロフィの高齢男性の1例2022

    • Author(s)
      四蔵梨奈、林孝彰、溝渕圭、田口諒、蕪城俊克、中野匡
    • Organizer
      第61回日本網膜硝子体学会総会
    • Related Report
      2022 Research-status Report
  • [Presentation] 日本人enhanced S-cone syndromeの臨床的および遺伝学的特徴2021

    • Author(s)
      林 孝彰
    • Organizer
      第125回日本眼科学会総会
    • Related Report
      2021 Research-status Report
  • [Presentation] SLC38A8遺伝子に1塩基挿入変異を認めた常染色体劣性黄斑低形成の1例2021

    • Author(s)
      林 孝彰
    • Organizer
      第46回日本小児眼科学会総会
    • Related Report
      2021 Research-status Report
  • [Presentation] 黄色斑眼底に類似したパターンジストロフィの1例2021

    • Author(s)
      齋藤友香、溝渕圭、林孝彰、郡司久人、中野匡
    • Organizer
      第75回日本臨床眼科学会
    • Related Report
      2021 Research-status Report
  • [Presentation] 日本における黄斑ジストロフィの患者発症数と総患者数の推定2021

    • Author(s)
      近藤峰生、上野真治、角田和繁、林孝彰、白澤誠、坂本泰二
    • Organizer
      第75回日本臨床眼科学会
    • Related Report
      2021 Research-status Report
  • [Presentation] インストラクションコース 網膜硝子体ジストロフィ診療カンファレンス2021

    • Author(s)
      近藤寛之、近藤峰生、林孝彰、高橋政代、堀田喜裕
    • Organizer
      第75回日本臨床眼科学会
    • Related Report
      2021 Research-status Report
  • [Book] 眼科検査ガイド 第3版2022

    • Author(s)
      林孝彰.遺伝子検査. 飯田知弘,近藤峰生,中村誠,山田昌和編
    • Total Pages
      6
    • Publisher
      文光堂
    • Related Report
      2022 Research-status Report
  • [Book] 黄斑疾患診療A to Z 第2版2022

    • Author(s)
      林孝彰.白点状眼底. 岸章治,吉村長久編
    • Total Pages
      6
    • Publisher
      医学書院
    • Related Report
      2022 Research-status Report
  • [Book] ファーストステップ!子どもの視機能をみる-スクリーニングと外来診療-2022

    • Author(s)
      林孝彰.仁科幸子,林思音編
    • Total Pages
      4
    • Publisher
      全日本病院出版会
    • Related Report
      2022 Research-status Report

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Published: 2021-04-28   Modified: 2025-01-30  

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