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ARVO Annual Meeting Abstract June 2021

Oculo-facio-cardio-dental (OFCD) syndrome: four cases in two Japanese families

Tomoyuki Yamazaki; Sho Naruse; Kentaro Kurata; Katsuhiro Hosono; Itsuka Matsushita; Atsushi Hiyoshi; Moriya Iwaizumi; Yoshiaki Kiuchi; Yoshihiro Hotta; Hiroyuki Kondo

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):1551. doi:

Articles June 2021

Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene

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Hiroyuki Kondo; Itsuka Matsushita; Tatsuo Nagata; Etsuko Fujihara; Katsuhiro Hosono; Eiichi Uchio; Yoshihiro Hotta; Shunji Kusaka
TAGS: familial exudative vitreoretinopathies, family, genes, mutation, eye, respiratory distress syndrome, newborn
Trans. Vis. Sci. Tech.. 2021; 10(7):18. doi: https://doi.org/10.1167/tvst.10.7.18

Includes: Supplemental Content

Articles May 2020

Polyethylene Glycol-Based Synthetic Hydrogel Sealant for Filtration Bleb Leaks: An In Vivo and Histologic Study

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Tatsuo Nagata; Yukinori Harada; Mikki Arai; Tatsuo Hirose; Hiroyuki Kondo
TAGS: blister, filtration, glycols, hydrogel, polyethylene, postoperative care, eye, surgical procedures, operative
Trans. Vis. Sci. Tech.. 2020; 9(6):24. doi: https://doi.org/10.1167/tvst.9.6.24

Retina March 2020

RDH5 -Related Fundus Albipunctatus in a Large Japanese Cohort

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Satoshi Katagiri; Takaaki Hayashi; Masaki Nakamura; Kei Mizobuchi; Tamaki Gekka; Shiori Komori; Shinji Ueno; Hiroko Terasaki; Hiroyuki Sakuramoto; Kazuki Kuniyoshi; Shunji Kusaka; Ryunosuke Nagashima; Mineo Kondo; Kaoru Fujinami; Kazushige Tsunoda; Tomokazu Matsuura; Hiroyuki Kondo; Kazutoshi Yoshitake; Takeshi Iwata; Tadashi Nakano
TAGS: cohort studies, japanese, pigmentary retinal dystrophy, electroretinography, eye, ophthalmoscopy, genetic pedigree, retinal cone
Invest. Ophthalmol. Vis. Sci.. 2020; 61(3):53. doi: https://doi.org/10.1167/iovs.61.3.53

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2019

Japan Eye Genetics Consortium: National Cohort Survey and Whole Exome Sequencing Results

Kaoru Fujinami; Kazutoshi Yoshitake; Takaaki Hayashi; Kazuki Kuniyoshi; Shinji Ueno; Mineo Kondo; Kei Shinoda; Shuhei Kameya; Nobuhisa Nao-i; Hiroyuki Kondo; Yozo Miyake; Takeshi Iwata; Kazushige Tsunoda

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):1758. doi:

ARVO Annual Meeting Abstract July 2018

Mutation Analysis of Japanese Patients with Leber Congenital Amaurosis by Next Generation Sequencing

Katsuhiro Hosono; Sachiko Nishina; Tadashi Yokoi; Satoshi Katagiri; Kentaro Kurata; Daisuke Miyamichi; Kei Mizobuchi; Tadashi Nakano; Shinsei Minoshima; Maki Fukami; Hiroyuki Kondo; Miho Sato; Takaaki Hayashi; Noriyuki Azuma; Yoshihiro Hotta

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5414. doi:

ARVO Annual Meeting Abstract June 2017

Defects in the cell signaling mediator β-catenin ( CTNNB1 ) cause the retinal vascular condition FEVR

Carmel Toomes; Evangelia S Panagiotou; James A. Poulter; Carla Sanjurjo Soriano; Hiroyuki Kondo; Atsushi Hiyoshi; Hon-Yin Brian Chung; Mark E Tafoya; Manir Ali; Chris F Inglehearn

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):2788. doi:

Genetics February 2017

A Japanese Family With Autosomal Dominant Oculocutaneous Albinism Type 4

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Ryoko Oki; Kisaburo Yamada; Satoko Nakano; Kenichi Kimoto; Ken Yamamoto; Hiroyuki Kondo; Toshiaki Kubota
TAGS: albinism, oculocutaneous, family, foveal hypoplasia, japanese, oculocutaneous albinism type 4, hypopigmentation disorder, genes, mutation, hair
Invest. Ophthalmol. Vis. Sci.. 2017; 58(2):1008-1016. doi: https://doi.org/10.1167/iovs.16-20612

Includes: Supplemental Content

ARVO Annual Meeting Abstract September 2016

Roles of genes in phenotypic diversity and intraocular asymmetry in patients with familial exudative vitreoretinopathy

Hiroyuki Kondo; Eiichi Uchio; Takaaki Hayashi; Sachiko Nishina; Noriyuki Azuma; Shunji Kusaka

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):2626. doi:

ARVO Annual Meeting Abstract June 2015

Mutations in ATOH7 gene in patients with congenital retinal detachment and familial exudative vitreoretinopathy

Hiroyuki Kondo; Itsuka Matsushita; Tomoko Tahira; Eiichi Uchio; Shunji Kusaka

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):3841. doi:

ARVO Annual Meeting Abstract June 2015

Persistence of metamorphopsia after vitrectomy for epiretinal membrane

Akihisa Watanabe; Hiroyuki Kondo

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):5058. doi:

ARVO Annual Meeting Abstract April 2014

Metamorphopsia after vitrectomy for macula-off rhegmatogenous retinal detachment.

Hirofumi Morita; Hiroyuki Kondo

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):1084. doi:

ARVO Annual Meeting Abstract April 2014

Safety of Anti-VEGF Drugs on Cultured Corneal Endothelial Cells

Tatsuo Nagata; Naoya Miyamoto; Hiroyuki Kondo

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):597. doi:

ARVO Annual Meeting Abstract June 2013

Repairing filtration bleb leakage with FocalSeal ® in rabbit model

Tatsuo Nagata; Yukinori Harada; Hiroyuki Kondo; Mikki Arai; Akihiko Tawara

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):4772. doi:

ARVO Annual Meeting Abstract March 2012

Tafluprost Protects Human Trabecular Meshwork Cells From Oxidative Stress Through The Activation Of C-myc/sirt1 Transcription Pathway

Naoya Miyamoto; Rie Miyamoto; Shingo Ishibashi; Hiroyuki Kondo; Akihiko Tawara

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):3226. doi:

ARVO Annual Meeting Abstract March 2012

Timolol Activates MMP9 Via Membrane-anchored Protease Regulator Reck In Human Trabecular Meshwork Cells

Rie Miyamoto; Naoya Miyamoto; Shingo Ishibashi; Hiroyuki Kondo; Akihiko Tawara

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):3231. doi:

ARVO Annual Meeting Abstract March 2012

New Mutation in GJA8 gene is Associated with Unique Phenotype of Familial Microphthalmia with Anomalies of Iris and Lens

Hiroyuki Kondo; Genji Nakamori; Eiichi Uchio; Tomoko Tahira; Ken Yamamoto; Akihiko Tawara

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):1541. doi:

ARVO Annual Meeting Abstract March 2012

Novel mutations in MFRP Gene in Japanese Patients with Microphthalmos

Itsuka Matsushita; Hiroyuki Kondo; Shingo Ishibashi; Tsutomu Ogata; Sachiko Nishina; Noriyuki Azuma; Akihiko Tawara

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):1544. doi:

ARVO Annual Meeting Abstract March 2012

Combined Exome Sequencing And Linkage Analysis Reveals A Dominant-negative ZNF408 Mutation Causing Familial Exudative Vitreoretinopathy

Rob W. Collin; Konstantinos Nikopoulos; Christian Gilissen; F Nienke Boonstra; Hiroyuki Kondo; Carmel Toomes; Wolfgang Berger; C Erik van Nouhuys; Alexander Hoischen; Frans P. Cremers

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):2257. doi:

ARVO Annual Meeting Abstract April 2011

Search For SOX17 Gene Mutations In Patients With Familial Exudative Vitreoretinopathy

Hiroyuki Kondo; Akihiko Tawara; Eiichi Uchio; Kenshi Hayashi; Tomoko Tahira

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):61. doi:

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Oculo-facio-cardio-dental (OFCD) syndrome: four cases in two Japanese families

Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene

Polyethylene Glycol-Based Synthetic Hydrogel Sealant for Filtration Bleb Leaks: An In Vivo and Histologic Study

RDH5 -Related Fundus Albipunctatus in a Large Japanese Cohort

Japan Eye Genetics Consortium: National Cohort Survey and Whole Exome Sequencing Results

Mutation Analysis of Japanese Patients with Leber Congenital Amaurosis by Next Generation Sequencing

Defects in the cell signaling mediator β-catenin ( CTNNB1 ) cause the retinal vascular condition FEVR

A Japanese Family With Autosomal Dominant Oculocutaneous Albinism Type 4

Roles of genes in phenotypic diversity and intraocular asymmetry in patients with familial exudative vitreoretinopathy

Mutations in ATOH7 gene in patients with congenital retinal detachment and familial exudative vitreoretinopathy

Persistence of metamorphopsia after vitrectomy for epiretinal membrane

Metamorphopsia after vitrectomy for macula-off rhegmatogenous retinal detachment.

Safety of Anti-VEGF Drugs on Cultured Corneal Endothelial Cells

Repairing filtration bleb leakage with FocalSeal ® in rabbit model

Tafluprost Protects Human Trabecular Meshwork Cells From Oxidative Stress Through The Activation Of C-myc/sirt1 Transcription Pathway

Timolol Activates MMP9 Via Membrane-anchored Protease Regulator Reck In Human Trabecular Meshwork Cells

New Mutation in GJA8 gene is Associated with Unique Phenotype of Familial Microphthalmia with Anomalies of Iris and Lens

Novel mutations in MFRP Gene in Japanese Patients with Microphthalmos

Combined Exome Sequencing And Linkage Analysis Reveals A Dominant-negative ZNF408 Mutation Causing Familial Exudative Vitreoretinopathy

Search For SOX17 Gene Mutations In Patients With Familial Exudative Vitreoretinopathy

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