Predicting mild familial exudative vitreoretinopathy with autosomal dominant inheritance using deep learning.
Waka Watanabe; Hideaki Mizoue; Itsuka Matsushita; Yoshiki Yasukochi; Koichiro Higasa; Hiroyuki Kondo
Scientific reports, Apr. 2026

Deletion involving exon 18 of RPGRIP1 is a major cause of achromatopsia.
Taiga Inooka; Kei Mizobuchi; Takaaki Hayashi; Akiko Suga; Kazushige Tsunoda; Kazuki Kuniyoshi; Hiroyuki Kondo; Junya Ota; Taro Kominami; Kazutoshi Yoshitake; Naoko Minematsu; Takeshi Iwata; Mineo Kondo; Koji M Nishiguchi; Shinji Ueno
Retina (Philadelphia, Pa.), Mar. 2026

EXCISION OF EXTENSIVE SUBRETINAL FIBROSIS ASSOCIATED WITH RHEGMATOGENOUS RETINAL DETACHMENTS IN PATIENTS WITH FAMILIAL EXUDATIVE VITREORETINOPATHY.
Hiroyuki Kondo; Itsuka Matsushita; Mizuki Tsurusaki
Retina (Philadelphia, Pa.), Feb. 2026

Comparing Rhegmatogenous and Tractional Retinal Detachment in Regressed Retinopathy of Prematurity: An International, Multicenter Study.
Han-Tung Hsu; Eugene Yu-Chuan Kang; Michael P Blair; Michael Shapiro; Rahul Komati; Baker G Hubbard; Kenneth W Price; Antonio Capone Jr; Kim A Drenser; Matthew G J Trese; Ryan Shields; Hiroyuki Kondo; Itsuka Matsushita; Yoshihiro Yonekawa; Samir N Patel; Shunji Kusaka; Fukutaro Mano; Karl R Olsen; Anna Ells; Atchara Amphornphruet; Mark K Walsh; Cagri G Besirli; Omar Moinuddin; Caroline R Baumal; Ana Bety Enriquez; Yih-Shiou Hwang; Chi-Chun Lai; Pin-Hsuan Huang; Wei-Chi Wu
American journal of ophthalmology, Feb. 2026

Autosomal dominant pigmented paravenous retinochoroidal atrophy associated with pathogenic variant in HK1 gene.
Kazuma Oku; Kei Mizobuchi; Kiyofumi Mochizuki; Kazushige Tsunoda; Itsuka Matsushita; Tatsuo Nagata; Kaoru Fujinami; Akiko Suga; Kazutoshi Yoshitake; Hirokazu Sakaguchi; Takaaki Hayashi; Takeshi Iwata; Hiroyuki Kondo
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, Jan. 2026

A novel deletion-insertion variant of RS1 in X-linked retinoschisis.
Natsuki Higa; Takaaki Hayashi; Kei Mizobuchi; Kazuki Kuniyoshi; Hiroyuki Kondo; Tadashi Nakano
Ophthalmic genetics, Dec. 2025

Retrospective multicentre study on functional vision score calculation using automated perimeter.
Mieko Tsuruoka; Yoshimune Hiratsuka; Kenji Inoue; Miki Murakami; Kazuma Oku; Hiroyuki Kondo; Mayumi Sainohira; Taiji Sakamoto; Akira Murakami
The British journal of ophthalmology, Sep. 2025

Fluorescein Angiography May Predict Surgical Outcomes of Tractional Retinal Detachment in Familial Exudative Vitreoretinopathy.
Tomoyuki Oga; Fukutaro Mano; Kazuki Kuniyoshi; Chiharu Iwahashi; Hiroyuki Kondo; Shunji Kusaka
Ophthalmology. Retina, Aug. 2025

Evaluation of the therapeutic effects of smoking cessation on chronic central serous chorioretinopathy.
Tatsuo Nagata; Nobuhisa Ochiai; Hiroyuki Kondo; Kazuma Oku; Mizuki Tsurusaki; Takuma Futami; Akihisa Watanabe; Itsuka Matsushita
Scientific reports, Jul. 2025

Two Cases of Rubinstein-Taybi Syndrome With Retinal Detachment.
Natsumi Kawaguchi; Fukutaro Mano; Hiroyuki Kondo; Kazuki Kuniyoshi; Shunij Kusaka
Cureus, Mar. 2025

Angiographic Characteristics in Mild Familial Exudative Vitreoretinopathy with Genetically Confirmed Autosomal Dominant Inheritance.
Misato Okamoto; Itsuka Matsushita; Tatsuo Nagata; Yoshihisa Fujino; Hiroyuki Kondo
Ophthalmology. Retina, Feb. 2025

Prevalence and incidence of Coats disease in a large claims database.
Nobuhisa Ochiai; Kenji Fujimoto; Kazuma Oku; Hiroyuki Kondo
PloS one, 2025

GENETIC ETIOLOGY AND CLINICAL FEATURES OF ACHROMATOPSIA IN JAPAN.
Taiga Inooka; Takaaki Hayashi; Kazushige Tsunoda; Kazuki Kuniyoshi; Hiroyuki Kondo; Kei Mizobuchi; Akiko Suga; Takeshi Iwata; Kazutoshi Yoshitake; Mineo Kondo; Kensuke Goto; Junya Ota; Taro Kominami; Koji M Nishiguchi; Shinji Ueno
Retina (Philadelphia, Pa.), Oct. 2024

Safety and efficacy of ripasudil eye drops in preterm infants with retinopathy of prematurity: phase 1/2, open label, single-arm trial.
Mitsuru Arima; Hirosuke Inoue; Akiko Misumi; Shoko Tsukamoto; Itsuka Matsushita; Shunsuke Araki; Manami Ohta; Kazumasa Takahashi; Miyuki Imazato; Tomoko Goto; Yoshinori Aoki; Koshiro Tagawa; Masayuki Hirose; Yuito Fujita; Noriko Yoshida; Shintaro Nakao; Hiroyuki Kondo; Koichi Kusuhara; Kazuhiro Kimura; Shunji Hasegawa; Yasuhiro Ikeda; Yuki Kodama; Hiroshi Moritake; Masayuki Ochiai; Shouichi Ohga; Junji Kishimoto; Koji Todaka; Ichiro Ieiri; Koh-Hei Sonoda
Japanese journal of ophthalmology, Sep. 2024

Association of variants in GJA8 with familial acorea-microphthalmia-cataract syndrome.
Shuqian Dong; Tongdan Zou; Fangyuan Zhen; Ting Wang; Yongwei Zhou; Jiahui Wu; Tatsuo Nagata; Itsuka Matsushita; Bo Gong; Hiroyuki Kondo; Qiuming Li; Houbin Zhang
European journal of human genetics : EJHG, Apr. 2024

A Pediatric Case of Disseminated Bartonella henselae Infection Accompanied by Multiple Intracranial Lesions.
Jun Hirakawa; Masaru Kawamura; Takayuki Hoshina; Madoka Taniguchi; Hiroyuki Kondo; Hiroshi Satake; Aya Nawata; Hidehiro Tsuneoka; Koichi Kusuhara
The Pediatric infectious disease journal, Feb. 2024

Measuring macular pigment optical density using reflective images of confocal scanning laser system.
Hirofumi Morita; Itsuka Matsushita; Yoshihisa Fujino; Akira Obana; Hiroyuki Kondo
Japanese journal of ophthalmology, Jan. 2024

Familial Exudative Vitreoretinopathy With and Without Pathogenic Variants of Norrin/β-Catenin Signaling Genes.
Hiroyuki Kondo; Tomoko Tsukahara-Kawamura; Itsuka Matsushita; Tatsuo Nagata; Takaaki Hayashi; Sachiko Nishina; Koichiro Higasa; Eiichi Uchio; Mineo Kondo; Taiji Sakamoto; Shunji Kusaka
Ophthalmology science, 2024

A novel RPE65 variant p.(Ala391Asp) in Leber congenital amaurosis: a case report and literature review in Japan.
Natsuki Higa; Takaaki Hayashi; Kei Mizobuchi; Maki Iwasa; Shingo Kubota; Kazuki Kuniyoshi; Shuhei Kameya; Hiroyuki Kondo; Mineo Kondo; Tadashi Nakano
Frontiers in medicine, 2024

OCULAR FEATURES ASSOCIATED WITH MUTATIONS IN ATOH7 GENE OVERLAP THOSE WITH FAMILIAL EXUDATIVE VITREORETINOPATHY.
Sho Naruse; Hiroyuki Kondo
Retinal cases & brief reports, Nov. 2023

Functional Characteristics of Diverse PAX6 Mutations Associated with Isolated Foveal Hypoplasia.
Itsuka Matsushita; Hiroto Izumi; Shinji Ueno; Takaaki Hayashi; Kaoru Fujinami; Kazushige Tsunoda; Takeshi Iwata; Yoshiaki Kiuchi; Hiroyuki Kondo
Genes, Jul. 2023

Reply.
Chiharu Iwahashi; Itsuka Matsushita; Kazuki Kuniyoshi; Hiroyuki Kondo; Shunji Kusaka
Retina (Philadelphia, Pa.), Jul. 2023

Late Vitreoretinal Complications of Regressed Retinopathy of Prematurity: Retinal Break, Vitreous Hemorrhage, and Retinal Detachment.
Han-Tung Hsu; Eugene Yu-Chuan Kang; Michael P Blair; Michael Shapiro; Rahul Komati; Baker G Hubbard; Kenneth W Price; Antonio Capone Jr; Kim A Drenser; Michael T Trese; Ryan Shields; Hiroyuki Kondo; Itsuka Matsushita; Yoshihiro Yonekawa; Samir N Patel; Shunji Kusaka; Fukutaro Mano; Karl R Olsen; Anna Ells; Atchara Amphornphruet; Mark K Walsh; Cagri G Besirli; Omar Moinuddin; Caroline R Baumal; Ana Bety Enriquez; Yih-Shiou Hwang; Chi-Chun Lai; Wei-Chi Wu
Ophthalmology. Retina, Jan. 2023

EFFICACY OF INNER WALL RETINECTOMY FOR BULLOUS SCHISIS CAVITY HANGING OVER OR THREATENING THE MACULA IN PATIENTS WITH CONGENITAL X-LINKED RETINOSCHISIS.
Chiharu Iwahashi; Itsuka Matsushita; Kazuki Kuniyoshi; Hiroyuki Kondo; Shunji Kusaka
Retina (Philadelphia, Pa.), Jan. 2023

Optical coherence tomography findings of the peripheral retina in patients with congenital X-linked retinoschisis.
Ayaka Nakajima; Kazuki Kuniyoshi; Chiharu Iwahashi; Fukutaro Mano; Takaaki Hayashi; Hiroyuki Kondo; Kei Mizobuchi; Itsuka Matsushita; Akiko Suga; Kazutoshi Yoshitake; Tadashi Nakano; Takeshi Iwata; Chota Matsumoto; Shunji Kusaka
Frontiers in medicine, 2023

Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing.
Akiko Suga; Kazutoshi Yoshitake; Naoko Minematsu; Kazushige Tsunoda; Kaoru Fujinami; Yozo Miyake; Kazuki Kuniyoshi; Takaaki Hayashi; Kei Mizobuchi; Shinji Ueno; Hiroko Terasaki; Taro Kominami; Nobuhisa Nao-I; Go Mawatari; Atsushi Mizota; Kei Shinoda; Mineo Kondo; Kumiko Kato; Tetsuju Sekiryu; Makoto Nakamura; Sentaro Kusuhara; Hiroyuki Yamamoto; Shuji Yamamoto; Kiyofumi Mochizuki; Hiroyuki Kondo; Itsuka Matsushita; Shuhei Kameya; Takeo Fukuchi; Tetsuhisa Hatase; Masayuki Horiguchi; Yoshiaki Shimada; Atsuhiro Tanikawa; Shuichi Yamamoto; Gen Miura; Nana Ito; Akira Murakami; Takuro Fujimaki; Yoshihiro Hotta; Koji Tanaka; Takeshi Iwata
Human mutation, Dec. 2022

Severe foveal hypoplasia and macular degeneration in Stickler syndrome caused by missense mutation in COL2A1 gene.
Mamika Asano; Katsuhiko Yokoyama; Kazuma Oku; Itsuka Matsushita; Kenichi Kimoto; Toshiaki Kubota; Hiroyuki Kondo
Ophthalmic genetics, Aug. 2022

Identification of Interphotoreceptor retinoid-binding protein in the Schisis cavity fluid of a patient with congenital X-linked Retinoschisis.
Fukutaro Mano; Koji Sugioka; Kazuki Kuniyoshi; Hiroyuki Kondo; Shunji Kusaka
BMC ophthalmology, Jan. 2022

Homozygous single nucleotide duplication of SLC38A8 in autosomal recessive foveal hypoplasia: The first Japanese case report.
Takaaki Hayashi; Hiroyuki Kondo; Itsuka Matsushita; Kei Mizobuchi; Akinori Baba; Kie Iida; Hiroyuki Kubo; Tadashi Nakano
Documenta ophthalmologica. Advances in ophthalmology, Dec. 2021

Genetic and Phenotypic Landscape of PRPH2-Associated Retinal Dystrophy in Japan.
Akio Oishi; Kaoru Fujinami; Go Mawatari; Nobuhisa Naoi; Yasuhiro Ikeda; Shinji Ueno; Kazuki Kuniyoshi; Takaaki Hayashi; Hiroyuki Kondo; Atsushi Mizota; Kei Shinoda; Sentaro Kusuhara; Makoto Nakamura; Takeshi Iwata; Akitaka Tsujikawa; Kazushige Tsunoda
Genes, Nov. 2021

Epidemiologic study of rhegmatogenous retinal detachment in Japan from the Diagnosis Procedure Combination database over a 2-year period (2014-2015).
Kazuma Oku; Kei Tokutsu; Shinya Matsuda; Hiroyuki Kondo
Japanese journal of ophthalmology, Nov. 2021

Familial exudative vitreoretinopathy with TGFBR2 mutation without signs of Loeys-Dietz syndrome.
Toshiaki Asano; Kazuma Oku; Hiroyuki Kondo
Ophthalmic genetics, Oct. 2021

Vitrectomy and external drainage of subretinal fluid containing high concentration of vascular endothelial growth factor for advanced coats disease.
Fukutaro Mano; Itsuka Matsushita; Hiroyuki Kondo; Shoko Utamura; Chiori Kondo; Shunji Kusaka
Scientific reports, Sep. 2021

Revesz syndrome with bilateral retinal detachments successfully treated by pars plana vitrectomy.
Mamika Asano; Shoko Tsukamoto; Koh-Hei Sonoda; Hiroyuki Kondo
American journal of ophthalmology case reports, Sep. 2021

Study protocol for a multicentre, open-label, single-arm phase I/II trial to evaluate the safety and efficacy of ripasudil 0.4% eye drops for retinopathy of prematurity.
Mitsuru Arima; Hirosuke Inoue; Shintaro Nakao; Akiko Misumi; Maya Suzuki; Itsuka Matsushita; Shunsuke Araki; Chiemi Yamashiro; Kazumasa Takahashi; Masayuki Ochiai; Noriko Yoshida; Masayuki Hirose; Junji Kishimoto; Koji Todaka; Shunji Hasegawa; Kazuhiro Kimura; Koichi Kusuhara; Hiroyuki Kondo; Shouichi Ohga; Koh-Hei Sonoda
BMJ open, Jul. 2021

Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene.
Hiroyuki Kondo; Itsuka Matsushita; Tatsuo Nagata; Etsuko Fujihara; Katsuhiro Hosono; Eiichi Uchio; Yoshihiro Hotta; Shunji Kusaka
Translational vision science & technology, Jun. 2021

Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN.
Kei Mizobuchi; Takaaki Hayashi; Noriko Oishi; Daiki Kubota; Shuhei Kameya; Koichiro Higasa; Takuma Futami; Hiroyuki Kondo; Katsuhiro Hosono; Kentaro Kurata; Yoshihiro Hotta; Kazutoshi Yoshitake; Takeshi Iwata; Tomokazu Matsuura; Tadashi Nakano
Journal of clinical medicine, May 2021

ULTRA-WIDE FIELD FUNDUS AUTOFLUORESCENCE IMAGING OF EYES WITH STICKLER SYNDROME.
Kazushi Fujimoto; Tatsuo Nagata; Itsuka Matsushita; Kazuma Oku; Mamika Imagawa; Kazuki Kuniyoshi; Takaaki Hayashi; Kenichi Kimoto; Masahito Ohji; Shunji Kusaka; Hiroyuki Kondo
Retina (Philadelphia, Pa.), Mar. 2021

Correlation between improvement in visual acuity and QOL after Ranibizumab treatment for age-related macular degeneration patients: QUATRO study.
Yuji Oshima; Yumi Ishibashi; Naoyasu Umeda; Tatsuo Nagata; Shigeo Yoshida; Eiichi Uchio; Hiroyuki Kondo; Koh-Hei Sonoda; Tatsuro Ishibashi
BMC ophthalmology, Jan. 2021

Autosomal dominant foveal hypoplasia without visible macular abnormalities and PAX6 mutations.
Itsuka Matsushita; Hirofumi Morita; Hiroyuki Kondo
Japanese journal of ophthalmology, Nov. 2020

Electroretinograms of eyes with Stickler syndrome.
Hiroyuki Kondo; Kazushi Fujimoto; Mamika Imagawa; Kazuma Oku; Itsuka Matsushita; Takaaki Hayashi; Tatsuo Nagata
Documenta ophthalmologica. Advances in ophthalmology, Jun. 2020

Polyethylene Glycol-Based Synthetic Hydrogel Sealant for Filtration Bleb Leaks: An In Vivo and Histologic Study.
Tatsuo Nagata; Yukinori Harada; Mikki Arai; Tatsuo Hirose; Hiroyuki Kondo
Translational vision science & technology, May 2020

RDH5-Related Fundus Albipunctatus in a Large Japanese Cohort.
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
Investigative ophthalmology & visual science, Mar. 2020

Early vitrectomy to reverse macular dragging in a one-month-old boy with familial exudative vitreoretinopathy.
Akiko Iwata; Shunji Kusaka; Mayumi Ishimaru; Hiroyuki Kondo; Kazuki Kuniyoshi
American journal of ophthalmology case reports, Sep. 2019

Novel mutations in the RS1 gene in Japanese patients with X-linked congenital retinoschisis.
Hiroyuki Kondo; Kazuma Oku; Satoshi Katagiri; Takaaki Hayashi; Tadashi Nakano; Akiko Iwata; Kazuki Kuniyoshi; Shunji Kusaka; Atsushi Hiyoshi; Eiichi Uchio; Mineo Kondo; Noriko Oishi; Shuhei Kameya; Atsushi Mizota; Nobuhisa Naoi; Shinji Ueno; Hiroko Terasaki; Takeshi Morimoto; Masayoshi Iwaki; Kazutoshi Yoshitake; Daisuke Iejima; Kaoru Fujinami; Kazushige Tsunoda; Kei Shinoda; Takeshi Iwata
Human genome variation, 2019

Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy.
Satoshi Katagiri; Maki Iwasa; Takaaki Hayashi; Katsuhiro Hosono; Takahiro Yamashita; Kazuki Kuniyoshi; Shinji Ueno; Mineo Kondo; Hisao Ueyama; Hisakazu Ogita; Yoshinori Shichida; Hidehito Inagaki; Hiroki Kurahashi; Hiroyuki Kondo; Masahito Ohji; Yoshihiro Hotta; Tadashi Nakano
Scientific reports, Jul. 2018

Risk allele of the FZD4 gene for familial exudative vitreoretinopathy.
Hiroyuki Kondo; Eiichi Uchio; Shunji Kusaka; Koichiro Higasa
Ophthalmic genetics, Jun. 2018

Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing.
Katsuhiro Hosono; Sachiko Nishina; Tadashi Yokoi; Satoshi Katagiri; Hirotomo Saitsu; Kentaro Kurata; Daisuke Miyamichi; Akiko Hikoya; Kei Mizobuchi; Tadashi Nakano; Shinsei Minoshima; Maki Fukami; Hiroyuki Kondo; Miho Sato; Takaaki Hayashi; Noriyuki Azuma; Yoshihiro Hotta
Scientific reports, May 2018

Lack of FOXE3 coding mutation in a case of congenital aphakia.
Yusuke Sano; Yusuke Matsukane; Akihisa Watanabe; Ko-Hei Sonoda; Hiroyuki Kondo
Ophthalmic genetics, 2018

Foveal hypoplasia and optical coherence tomographic imaging.
Hiroyuki Kondo
Taiwan journal of ophthalmology, 2018

Foveal Hypoplasia in Patients with Stickler Syndrome.
Itsuka Matsushita; Tatsuo Nagata; Takaaki Hayashi; Kenichi Kimoto; Toshiaki Kubota; Masahito Ohji; Shunji Kusaka; Hiroyuki Kondo
Ophthalmology, Jun. 2017

Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
Evangelia S Panagiotou; Carla Sanjurjo Soriano; James A Poulter; Emma C Lord; Denisa Dzulova; Hiroyuki Kondo; Atsushi Hiyoshi; Brian Hon-Yin Chung; Yoyo Wing-Yiu Chu; Connie H Y Lai; Mark E Tafoya; Dyah Karjosukarso; Rob W J Collin; Joanne Topping; Louise M Downey; Manir Ali; Chris F Inglehearn; Carmel Toomes
American journal of human genetics, Jun. 2017

Correspondence.
Bozho Todorich; Aristomenis Thanos; Yoshihiro Yonekawa; Benjamin J Thomas; Lisa J Faia; Emmanuel Chang; Julia Shulman; Karl R Olsen; Michael P Blair; Michael P Shapiro; Philip Ferrone; Lejla Vajzovic; Cynthia A Toth; Thomas C Lee; Joshua Robinson; Baker Hubbard; Hiroyuki Kondo; Cagri G Besirli; Eric Nudleman; Sui Chien Wong; Shunji Kusaka; Mark Walsh; R V Paul Chan; Audina Berrocal; George Caputo; Timothy G Murray; Jonathan Sears; Roberto Schunemann; Clio A Harper 3rd; Andres Kychental; Paola Dorta; Linda A Cernichiaro-Espinosa; Wei-Chi Wu; J Peter Campbell; Maria A Martinez-Castellanos; Hugo Quiroz-Mercado; Hidyuki Hayashi; Polly Quiram; Atchara Amphornphruet; Mary E Hartnett; Irena Tsui; Anna Ells; Vishak John; Darius Moshfeghi; Antonio Capone Jr; Kimberly A Drenser; Michael T Trese
Retina (Philadelphia, Pa.), May 2017

A Japanese Family With Autosomal Dominant Oculocutaneous Albinism Type 4.
Ryoko Oki; Kisaburo Yamada; Satoko Nakano; Kenichi Kimoto; Ken Yamamoto; Hiroyuki Kondo; Toshiaki Kubota
Investigative ophthalmology & visual science, Feb. 2017

[Color Functionality Used in Visual Display for Occupational and Environmental Safety and Managing Color Vision Deficiency].
Nobuhisa Ochiai; Hiroyuki Kondo
Journal of UOEH, 2017

Mutations in ATOH7 gene in patients with nonsyndromic congenital retinal nonattachment and familial exudative vitreoretinopathy.
Hiroyuki Kondo; Itsuka Matsushita; Tomoko Tahira; Eiichi Uchio; Shunji Kusaka
Ophthalmic genetics, Dec. 2016

Properties of new diffusion filters for treatment of amblyopia with accurate occlusive effects.
Makoto Sasaki; Tsuneto Iwasaki; Hiroyuki Kondo; Akihiko Tawara
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, Jun. 2016

Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy.
James A Poulter; Manir Ali; David F Gilmour; Aine Rice; Hiroyuki Kondo; Kenshi Hayashi; David A Mackey; Lisa S Kearns; Jonathan B Ruddle; Jamie E Craig; Eric A Pierce; Louise M Downey; Moin D Mohamed; Alexander F Markham; Chris F Inglehearn; Carmel Toomes
American journal of human genetics, Mar. 2016

Novel mutations in the COL2A1 gene in Japanese patients with Stickler syndrome.
Hiroyuki Kondo; Itsuka Matsushita; Tatsuo Nagata; Takaaki Hayashi; Masashi Kakinoki; Eiichi Uchio; Mineo Kondo; Masahito Ohji; Shunji Kusaka
Human genome variation, 2016

[Effect of Intravitreal Bevacizumab Injection on Iris and Iridocorneal Angle Neovascularization in Neovascular Glaucoma].
Shingo Ishibashi; Hiroyuki Kondo
Journal of UOEH, Dec. 2015

[An Evaluation of Visual Function in Working Age Patients with Glaucoma].
Miki Murakami; Yasuko Obata; Hiroshi Yamato; Hiroyuki Kondo
Journal of UOEH, Sep. 2015

Submicroscopic deletions at 13q32.1 cause congenital microcoria.
Lucas Fares-Taie; Sylvie Gerber; Akihiko Tawara; Arturo Ramirez-Miranda; Jean-Yves Douet; Hannah Verdin; Antoine Guilloux; Juan C Zenteno; Hiroyuki Kondo; Hugo Moisset; Bruno Passet; Ken Yamamoto; Masaru Iwai; Toshihiro Tanaka; Yusuke Nakamura; Wataru Kimura; Christine Bole-Feysot; Marthe Vilotte; Sylvie Odent; Jean-Luc Vilotte; Arnold Munnich; Alain Regnier; Nicolas Chassaing; Elfride De Baere; Isabelle Raymond-Letron; Josseline Kaplan; Patrick Calvas; Olivier Roche; Jean-Michel Rozet
American journal of human genetics, Apr. 2015

Complex genetics of familial exudative vitreoretinopathy and related pediatric retinal detachments.
Hiroyuki Kondo
Taiwan journal of ophthalmology, 2015

[Questionnaire survey of ocular injuries due to fireworks in Japan].
Akihiko Tawara; Akihisa Watanabe; Ayuko Endo; Hiroyuki Kondo
Nippon Ganka Gakkai zasshi, Dec. 2014

The effects of a convex rear-view mirror on ocular accommodative responses.
Tatsuo Nagata; Tsuneto Iwasaki; Hiroyuki Kondo; Akihiko Tawara
Applied ergonomics, Nov. 2013

Familial acorea, microphthalmia and cataract syndrome.
Hiroyuki Kondo; Tomoko Tahira; Ken Yamamoto; Akihiko Tawara
The British journal of ophthalmology, Sep. 2013

Reconstruction of a nonfunctional trabeculectomy bleb using an amniotic membrane-wrapped silicone sponge to treat refractory glaucoma.
Akihiko Tawara; Naoya Miyamoto; Shingo Ishibashi; Tatsuo Nagata; Yukinori Harada; Norihiko Tou; Hiroyuki Kondo
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, Aug. 2013

Long-term changes in corneal endothelial cell density after repeat penetrating keratoplasty in eyes with endothelial decompensation.
Ken Hayashi; Hiroyuki Kondo; Aya Maeno; Minehiro Takimoto
Cornea, Jul. 2013

ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature.
Rob W J Collin; Konstantinos Nikopoulos; Margo Dona; Christian Gilissen; Alexander Hoischen; F Nienke Boonstra; James A Poulter; Hiroyuki Kondo; Wolfgang Berger; Carmel Toomes; Tomoko Tahira; Lucas R Mohn; Ellen A Blokland; Lisette Hetterschijt; Manir Ali; Johanne M Groothuismink; Lonneke Duijkers; Chris F Inglehearn; Lea Sollfrank; Tim M Strom; Eiichi Uchio; C Erik van Nouhuys; Hannie Kremer; Joris A Veltman; Erwin van Wijk; Frans P M Cremers
Proceedings of the National Academy of Sciences of the United States of America, Jun. 2013

Corneal endothelial damage after cataract surgery in eyes with pseudoexfoliation syndrome.
Ken Hayashi; Shin-Ichi Manabe; Koichi Yoshimura; Hiroyuki Kondo
Journal of cataract and refractive surgery, Jun. 2013

A classic temporal optic disc pit showing progression in the corresponding optic nerve fiber and visual field defects.
Akihiko Tawara; Rie Miyamoto; Norihiko Tou; Shingo Ishibashi; Hiroyuki Kondo
Japanese journal of ophthalmology, May 2013

Identification of causative pathogens in eyes with bacterial conjunctivitis by bacterial cell count and microbiota analysis.
Rumi Aoki; Kazumasa Fukuda; Midori Ogawa; Takako Ikeno; Hiroyuki Kondo; Akihiko Tawara; Hatsumi Taniguchi
Ophthalmology, Apr. 2013

Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity.
Hiroyuki Kondo; Shunji Kusaka; Aki Yoshinaga; Eiichi Uchio; Akihiko Tawara; Tomoko Tahira
Molecular vision, 2013

Novel compound heterozygous mutations in the MFRP gene in a Japanese patient with posterior microphthalmos.
Itsuka Matsushita; Hiroyuki Kondo; Akihiko Tawara
Japanese journal of ophthalmology, Jul. 2012

Higher-order aberrations and visual function in pseudophakic eyes with a toric intraocular lens.
Ken Hayashi; Hiroyuki Kondo; Motoaki Yoshida; Shin-ichi Manabe; Akira Hirata
Journal of cataract and refractive surgery, Jul. 2012

Survey of microphthalmia in Japan.
Sachiko Nishina; Daijiro Kurosaka; Yasuhiro Nishida; Hiroyuki Kondo; Yuri Kobayashi; Noriyuki Azuma
Japanese journal of ophthalmology, May 2012

Mutations in the TSPAN12 gene in Japanese patients with familial exudative vitreoretinopathy.
Hiroyuki Kondo; Shunji Kusaka; Aki Yoshinaga; Eiichi Uchio; Akihiko Tawara; Kenshi Hayashi; Tomoko Tahira
American journal of ophthalmology, Jun. 2011

Transcriptional regulation of activating transcription factor 4 under oxidative stress in retinal pigment epithelial ARPE-19/HPV-16 cells.
Naoya Miyamoto; Hiroto Izumi; Rie Miyamoto; Han Bin; Hiroyuki Kondo; Akihiko Tawara; Yasuyuki Sasaguri; Kimitoshi Kohno
Investigative ophthalmology & visual science, Mar. 2011

Quercetin induces the expression of peroxiredoxins 3 and 5 via the Nrf2/NRF1 transcription pathway.
Naoya Miyamoto; Hiroto Izumi; Rie Miyamoto; Hiroyuki Kondo; Akihiko Tawara; Yasuyuki Sasaguri; Kimitoshi Kohno
Investigative ophthalmology & visual science, Feb. 2011

A case of Fukuyama congenital muscular dystrophy associated with negative electroretinograms.
Hiroyuki Kondo; Kayoko Saito; Mari Urano; Yukiko Sagara; Eiichi Uchio; Mineo Kondo
Japanese journal of ophthalmology, Nov. 2010

Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.
James A Poulter; Manir Ali; David F Gilmour; Aine Rice; Hiroyuki Kondo; Kenshi Hayashi; David A Mackey; Lisa S Kearns; Jonathan B Ruddle; Jamie E Craig; Eric A Pierce; Louise M Downey; Moin D Mohamed; Alexander F Markham; Chris F Inglehearn; Carmel Toomes
American journal of human genetics, Feb. 2010

Late recurrence of retinal detachment following successful vitreous surgery for stages 4B and 5 retinopathy of prematurity.
Hiroyuki Kondo; Naoko Arita; Masahiko Osato; Hideyuki Hayashi; Kenji Oshima; Eiichi Uchio
American journal of ophthalmology, Apr. 2009

Lens-sparing vitrectomy effective for reattachment of newly developed falciform retinal detachment in a patient with Norrie disease.
Chiharu Shima; Shunji Kusaka; Hiroyuki Kondo; Haruyuki Hasebe; Takashi Fujikado; Yasuo Tano
Archives of ophthalmology (Chicago, Ill. : 1960), Apr. 2009

Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy.
Minghui Qin; Hiroyuki Kondo; Tomoko Tahira; Kenshi Hayashi
Human genetics, Jan. 2008

Severe form of familial exudative vitreoretinopathy caused by homozygous R417Q mutation in frizzled-4 gene.
Hiroyuki Kondo; Minghui Qin; Tomoko Tahira; Eiichi Uchio; Kenshi Hayashi
Ophthalmic genetics, Dec. 2007

Novel mutations in Norrie disease gene in Japanese patients with Norrie disease and familial exudative vitreoretinopathy.
Hiroyuki Kondo; Minghui Qin; Shunji Kusaka; Tomoko Tahira; Haruyuki Hasebe; Hideyuki Hayashi; Eiichi Uchio; Kenshi Hayashi
Investigative ophthalmology & visual science, Mar. 2007

A case of incontinentia pigmenti in Japan and its genetic examination.
Jane Huang; Hiroyuki Kondo; Eiichi Uchio
Japanese journal of ophthalmology, 2007

Novel OPA1 mutations identified in Japanese pedigrees with optic atrophy.
Minghui Qin; Hiroyuki Kondo; Hideaki Uno; Eriko Fujiwara; Eiichi Uchio; Tomoko Tahira; Kenshi Hayashi
Molecular vision, May 2006

Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes.
Minghui Qin; Hideyuki Hayashi; Kenji Oshima; Tomoko Tahira; Kenshi Hayashi; Hiroyuki Kondo
Human mutation, Aug. 2005

A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa, using microsatellite markers.
Hiroyuki Kondo; Minghui Qin; Atsushi Mizota; Mineo Kondo; Hideyuki Hayashi; Ken Hayashi; Kenji Oshima; Tomoko Tahira; Kenshi Hayashi
Investigative ophthalmology & visual science, Dec. 2004

Diagnosis of autosomal dominant retinitis pigmentosa by linkage-based exclusion screening with multiple locus-specific microsatellite markers.
Hiroyuki Kondo; Tomoko Tahira; Atsushi Mizota; Emiko Adachi-Usami; Kenji Oshima; Kenshi Hayashi
Investigative ophthalmology & visual science, Mar. 2003

Non-paralleled increase of hepatocyte growth factor and vascular endothelial growth factor in the eyes with angiogenic and nonangiogenic fibroproliferation.
Naoyasu Umeda; Hiroaki Ozaki; Hideyuki Hayashi; Hiroyuki Kondo; Hiroko Uchida; Kenji Oshima
Ophthalmic research, 2002

【知っておきたい稀な網膜・硝子体ジストロフィ】家族性滲出性硝子体網膜症と関連疾患
近藤 寛之
OCULISTA, Jun. 2019, Reviewed, Null
Lead

【眼科医のための救急マニュアル】 薬物による眼科救急
石橋 真吾, 近藤 寛之
OCULISTA, Nov. 2016, Reviewed, Null
Last

【網膜剥離の診療プラクティス】 小児網膜剥離　ROP鎮静後、FEVR、朝顔症候群など
近藤 寛之
OCULISTA, Jun. 2016, Reviewed, Null
Lead

【徹底的に基本を学ぶ!子どもの眼の手術入門-術前計画・麻酔・手技・術後ケア-】小児硝子体手術の術前計画・麻酔・手技・術後ケア
近藤 寛之
OCULISTA, Oct. 2024, Null, Null
Lead

【ステップアップ!黄斑疾患診療-コツとピットフォールを中心に-】若年性網膜分離症
近藤 寛之
OCULISTA, Aug. 2022, Null, Null
Lead

PAX6遺伝子のストップゲイン変異による無虹彩症の1例
福永 直子, 林 孝彰, 飯田 由佳, 徳久 照朗, 比嘉 奈津貴, 松下 五佳, 近藤 寛之, 中野 匡
あたらしい眼科, Jul. 2024, Null, Null

【小児の網膜疾患】家族性滲出性硝子体網膜症
近藤 寛之
あたらしい眼科, Jul. 2024, Null, Null
Lead

小児の網膜電図記録用に新しく試作した極小LED内蔵コンタクトレンズ電極の使用経験
永濱 皆美, 奥 一真, 近藤 寛之
あたらしい眼科, Jul. 2021, Reviewed, No invitation
Last, Corresponding

小児の真性小眼球症の黄斑隆起所見
浅野 真美加, 近藤 寛之
あたらしい眼科, Nov. 2021, Reviewed, No invitation
Last, Corresponding

網膜変性診療の未来予想図
近藤寛之,　近藤峰生
あたらしい眼科, Apr. 2018, Reviewed, Null
Lead

【あなたはゲノムをみて診療をしますか?】 小児眼科
近藤 寛之
あたらしい眼科, Jul. 2017, Reviewed, Null
Lead

プロスタグランジン関連点眼薬から1%ドルゾラミド/0.5%チモロール配合点眼薬への切り替え効果
石橋 真吾, 永田 竜朗, 近藤 寛之, 落合 信寿
あたらしい眼科, Apr. 2017, Reviewed, Null

【小児眼科Q&A】 先天性疾患・小児疾患　網膜異常をきたすおもな先天疾患とその対処を教えてください
近藤 寛之
あたらしい眼科, Nov. 2016, Reviewed, Null
Lead

【子どものあたま、かお、くびの病気〜コンサルのタイミング】眼・眼囲　斜視・弱視
近藤 寛之
小児科診療, Aug. 2019, Reviewed, Null
Lead

遺伝性網膜ジストロフィにおける遺伝学的検査のガイドラインについて
近藤 寛之
日本の眼科, Jun. 2024, Null, Null
Lead

眼科医の手引　高解像度OCTでみえてくるもの　新しい黄斑低形成の概念
近藤 寛之
日本の眼科, Mar. 2018, Reviewed, Null
Lead

自動車運転が課題となった脳梗塞後の半盲の一例
村上 美紀, 奥 一真, 蜂須賀 研二, 近藤 寛之
日本ロービジョン学会誌, Mar. 2019, Reviewed, Null
Last

治療法の再整理とアップデートのために　専門家による私の治療　未熟児網膜症
近藤 寛之
日本医事新報, Aug. 2023, Not reviewed, Invited
Lead

網膜分離症を契機に発見された網膜色素変性の1例
谷口 円香, 浅野 真美加, 松下 五佳, 近藤 寛之
日本眼科学会雑誌, Oct. 2024, Null, Null
Corresponding

遺伝性網膜ジストロフィにおける遺伝学的検査のガイドライン
池田 康博, 堀田 喜裕, 近藤 寛之, 西口 康二, 前田 亜希子, 藤波 芳, 大石 明生, 三宅 正裕, 秋山 雅人, 厚生労働科学研究費補助金難治性疾患政策研究事業網膜脈絡膜・視神経萎縮症に関する調査研究班遺伝性網膜ジストロフィにおける遺伝学的検査のガイドライン作成ワーキンググループ
日本眼科学会雑誌, Jun. 2023, Reviewed, Null

未熟児網膜症に対する抗VEGF療法の手引き(第2版)
寺崎 浩子, 東 範行, 北岡 隆, 日下 俊次, 近藤 寛之, 仁科 幸子, 盛 隆興, 山田 昌和, 吉冨 健志, 未熟児網膜症眼科管理対策委員会, 日本眼科学会, 日本網膜硝子体学会, 日本小児眼科学会, 日本眼科医会
日本眼科学会雑誌, May 2023, Reviewed, Null

ゲノム医療をめざして　眼遺伝学の研究と臨床
堀田 喜裕, 佐藤 美保, 彦谷 明子, 永瀬 康規, 須藤 希実子, 細野 克博, 倉田 健太郎, 古森 美和, 立花 信貴, 鳥居 薫子, 中西 啓, 蓑島 伸生, 王 春霞, 大坪 正史, 大石 健太郎, 才津 浩智, 東 範行, 仁科 幸子, 横井 匡, 林 孝彰, 片桐 聡, 溝渕 圭, 中野 匡, 高橋 政代, 近藤 寛之
日本眼科学会雑誌, Mar. 2023, Reviewed, Null
Last, Corresponding

PAX6標的遺伝子の検索と孤立性黄斑低形成症例における関与
松下 五佳, 和泉 弘人, 近藤 寛之
日本眼科学会雑誌, Mar. 2022, Null, Null
Last

意外と見逃している?網脈絡膜ジストロフィ
近藤 寛之
日本眼科学会雑誌, Jun. 2022, Null, Null
Lead

小児網膜疾患の診断と治療
近藤 寛之
日本視機能看護学会誌, Oct. 2024, Null, Null
Lead

産業・環境安全のための視覚表示に用いる色彩の機能性と色覚異常への対応
落合 信寿, 近藤 寛之
産業医科大学雑誌, Mar. 2017, Reviewed, Null

就労年齢における緑内障患者の視機能評価
村上 美紀, 小畑 泰子, 大和 浩, 近藤 寛之
産業医科大学雑誌, Sep. 2015, Reviewed, Null
Last

A case of retinitis pigmentosa with cytomegalovirus chronic retinal necrosis during treatment of systemic lupus erythematosus
野田 啓司, 浅野 真美加, 近藤 寛之
眼科, Mar. 2025, Reviewed, No invitation
Corresponding

全エクソームシークエンシングで原因が確定できなかった眼底が正常な錐体杆体ジストロフィの1例
二見 拓磨, 永田 竜朗, 近藤 寛之
眼科, Sep. 2024, Null, Null
Corresponding

【変わりつつある網膜剥離の常識】小児の網膜剥離の動向
近藤 寛之
眼科, Sep. 2023, Not reviewed, Invited
Lead

【眼疾患のガイドラインと診療指針解説とアップデート】家族性滲出性硝子体網膜症(の診療の手引き)
近藤 寛之
眼科, Dec. 2022, Null, Null
Lead

網膜下に増殖性病変を生じたVogt-小柳-原田病の1例
浅野 利彰, 渡部 晃久, 近藤 寛之
眼科, Aug. 2021, Reviewed, No invitation
Last, Corresponding

【分子標的薬と眼】抗VEGF剤の眼科応用の現状　未熟児網膜症
近藤 寛之
眼科, Apr. 2019, Reviewed, Null
Lead

抗VEGF剤の眼科応用の現状：未熟児網膜症
近藤　寛之
眼科, Apr. 2019, Reviewed, Null
Lead

未熟児網膜症の最新の治療「光凝固と抗VEGF剤について」
近藤　寛之
眼科, Jul. 2018, Reviewed, No invitation
Lead

【眼科手術の適応-最新情報】 網膜硝子体　未熟児網膜症のレーザー光凝固と手術
近藤 寛之
眼科, Sep. 2017, Reviewed, Null
Lead

小児眼科疾患　家族性滲出性硝子体網膜症　Familial exudative vitreoretinopathy
近藤 寛之
眼科, Jan. 2017, Reviewed, Null
Lead

【視神経乳頭　異常所見のすべて】 視神経の先天異常
近藤 寛之
眼科グラフィック, Apr. 2018, Reviewed, Null
Lead

難渋症例にチャレンジ!眼科診断トレーニング　家族性滲出性硝子体網膜症
近藤 寛之
眼科グラフィック, Jun. 2023, Not reviewed, Invited
Lead

難渋症例にチャレンジ!眼科診断トレーニング　コーツ病(Coats disease)
近藤 寛之
眼科グラフィック, Jun. 2022, Null, Null
Lead

【小児の網膜硝子体手術】小児の硝子体剥離
近藤 寛之
眼科手術, Apr. 2024, Null, Null
Lead

手術相談室　症例呈示　Marfan症候群小児の脱臼水晶体切除の適応,術式ならびに術後屈折矯正の選択は?
林 英之, 根岸 一乃, 永田 万由美, 松下 五佳, 近藤 寛之, 太田 俊彦
眼科手術, Oct. 2023, Not reviewed, Invited

小児穿孔性眼外傷の診断と手術治療
成瀬 翔, 近藤 寛之
眼科手術, Oct. 2023, Not reviewed, Invited
Last, Corresponding

小児の家族性滲出性硝子体網膜症に続発した急性緑内障発作の一例
高尾 瑞季, 浅野 利彰, 成瀬 翔, 近藤 寛之
眼科臨床紀要, Apr. 2024, Null, Null
Corresponding

FVS(Functional Vision Score)中心暗点ルール適応前後のFVSスコアとAMAクラス
村上 美紀, 石橋 真吾, 近藤 寛之
眼科臨床紀要, Mar. 2019, Reviewed, Null
Last

高校での学習支援が得られた杆体錐体ジストロフィの1例　視機能と情報提供
村上 美紀, 近藤 寛之
眼科臨床紀要, Jan. 2019, Reviewed, Null

X染色体若年網膜分離症患者におけるFunctional Vision Scoreの評価
村上 美紀, 近藤 寛之
眼科臨床紀要, May 2018, Reviewed, Null
Last

アトピー性皮膚炎患者に対する硝子体手術施行例の外眼部所見
成瀬 翔, 近藤 寛之, 奥 一真, 森田 啓文
眼科臨床紀要, May 2018, Reviewed, Null

自動車運転が課題となった脳梗塞後の半盲の一例
村上 美紀, 奥 一真, 蜂須賀 研二, 近藤 寛之
眼科臨床紀要, Dec. 2018, Reviewed, Null
Last

視覚障害者における交通事故の特徴分析
落合 信寿, 村上 美紀, 高橋 広, 近藤 寛之
眼科臨床紀要, Sep. 2017, Reviewed, Null
Corresponding

産業医科大学における小児のロービジョンケア　ロービジョン外来開設10ヵ月の報告
村上 美紀, 井上 久美, 山本 久美子, 永濱 皆美, 近藤 寛之
眼科臨床紀要, May 2017, Reviewed, Null
Corresponding

水晶体亜脱臼を伴う低眼圧症に対し、眼内レンズ毛様溝縫着術が奏効した3例
奥 一真, 真野 奈津子, 喜田 照代, 池田 恒彦, 近藤 寛之
眼科臨床紀要, Mar. 2017, Reviewed, Null
Last

汎網膜光凝固後で交感性眼炎の診断が困難であった1例
渕野 仁志, 永田 竜朗, 高田 実乃梨, 浅野 利彰, 近藤 寛之
臨床眼科, Jul. 2024, Null, Null
Corresponding

嚢胞様腔内フィブリノゲン塊摘出術が奏効した黄斑部毛細血管拡張症1型
高田 実乃梨, 永田 竜朗, 古泉 英貴, 近藤 寛之
臨床眼科, Aug. 2023, Reviewed, No invitation
Last, Corresponding

【日本の眼の難病-何がどこまでわかってきたのか?】家族性滲出性硝子体網膜症
近藤 寛之
臨床眼科, Jan. 2023, Not reviewed, Invited
Lead

視覚障害者の就労支援ツールの開発(第2報)　改良支援ツールと輪状暗点
高橋 広, 氏間 和仁, 岩井 克之, 村上 美紀, 山田 敏夫, 吉田 治, 山田 信也, 落合 信寿, 近藤 寛之
臨床眼科, Oct. 2021, Reviewed, Null
Last

意図的巨大裂孔作成が奏効した巨大網膜嚢胞を伴うアトピー性網膜剥離
西村 太吾, 奥 一真, 近藤 寛之
臨床眼科, May 2019, Reviewed, Null
Last

臨床報告 マイラゲルの術中強膜穿孔に強膜短縮術が有効であった1症例
松金 祐介, 伊東 健, 近藤 寛之
臨床眼科, Aug. 2016, Reviewed, Null

Pituitary Macroadenoma and Visual Impairment: Postoperative Outcome Prediction with Contrast-Enhanced FIESTA.
Hisanaga S, Kakeda S, Yamamoto J, Watanabe K, Moriya J, Nagata T, Fujino Y, Kondo H, Nishizawa S, Korogi Y
AJNR. American journal of neuroradiology, Sep. 2017, Reviewed, Null

Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
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
American journal of human genetics, Jun. 2017, Reviewed, Null

Mutations in the TSPAN12 gene in Japanese patients with familial exudative vitreoretinopathy.
Kondo Hiroyuki, Kusaka Shunji, Yoshinaga Aki, Uchio Eiichi, Tawara Akihiko, Hayashi Kenshi, Tahira Tomoko
American journal of ophthalmology, Jun. 2011, Reviewed, Null
Lead

Revesz syndrome with bilateral retinal detachments successfully treated by pars plana vitrectomy.
Asano Mamika, Tsukamoto Shoko, Sonoda Koh-Hei, Kondo Hiroyuki
American journal of ophthalmology case reports, Sep. 2021, Reviewed, Null
Last, Corresponding

Early vitrectomy to reverse macular dragging in a one-month-old boy with familial exudative vitreoretinopathy.
Iwata Akiko, Kusaka Shunji, Ishimaru Mayumi, Kondo Hiroyuki, Kuniyoshi Kazuki
American journal of ophthalmology case reports, Sep. 2019, Reviewed, Null

Identification of Interphotoreceptor retinoid-binding protein in the Schisis cavity fluid of a patient with congenital X-linked Retinoschisis.
Mano Fukutaro, Sugioka Koji, Kuniyoshi Kazuki, Kondo Hiroyuki, Kusaka Shunji
BMC ophthalmology, Jan. 2022, Null, Null

Correlation between improvement in visual acuity and QOL after Ranibizumab treatment for age-related macular degeneration patients: QUATRO study.
Oshima Yuji, Ishibashi Yumi, Umeda Naoyasu, Nagata Tatsuo, Yoshida Shigeo, Uchio Eiichi, Kondo Hiroyuki, Sonoda Koh-Hei, Ishibashi Tatsuro
BMC ophthalmology, Jan. 2021, Reviewed, No invitation

Study protocol for a multicentre, open-label, single-arm phase I/II trial to evaluate the safety and efficacy of ripasudil 0.4% eye drops for retinopathy of prematurity.
Arima Mitsuru, Inoue Hirosuke, Nakao Shintaro, Misumi Akiko, Suzuki Maya, Matsushita Itsuka, Araki Shunsuke, Yamashiro Chiemi, Takahashi Kazumasa, Ochiai Masayuki, Yoshida Noriko, Hirose Masayuki, Kishimoto Junji, Todaka Koji, Hasegawa Shunji, Kimura Kazuhiro, Kusuhara Koichi, Kondo Hiroyuki, Ohga Shouichi, Sonoda Koh-Hei
BMJ open, Jul. 2021, Reviewed, No invitation

Homozygous single nucleotide duplication of SLC38A8 in autosomal recessive foveal hypoplasia: The first Japanese case report.
Hayashi Takaaki, Kondo Hiroyuki, Matsushita Itsuka, Mizobuchi Kei, Baba Akinori, Iida Kie, Kubo Hiroyuki, Nakano Tadashi
Documenta ophthalmologica. Advances in ophthalmology, Dec. 2021, Reviewed, No invitation

Electroretinograms of eyes with Stickler syndrome.
Kondo Hiroyuki, Fujimoto Kazushi, Imagawa Mamika, Oku Kazuma, Matsushita Itsuka, Hayashi Takaaki, Nagata Tatsuo
Documenta ophthalmologica. Advances in ophthalmology, Jun. 2020, Reviewed, Null
Lead

Association of variants in GJA8 with familial acorea-microphthalmia-cataract syndrome.
Dong Shuqian, Zou Tongdan, Zhen Fangyuan, Wang Ting, Zhou Yongwei, Wu Jiahui, Nagata Tatsuo, Matsushita Itsuka, Gong Bo, Kondo Hiroyuki, Li Qiuming, Zhang Houbin
European journal of human genetics : EJHG, Apr. 2024, Reviewed, No invitation

Functional Characteristics of Diverse PAX6 Mutations Associated with Isolated Foveal Hypoplasia.
Matsushita Itsuka, Izumi Hiroto, Ueno Shinji, Hayashi Takaaki, Fujinami Kaoru, Tsunoda Kazushige, Iwata Takeshi, Kiuchi Yoshiaki, Kondo Hiroyuki
Genes, Jul. 2023, Reviewed, No invitation
Last, Corresponding

Genetic and Phenotypic Landscape of PRPH2-Associated Retinal Dystrophy in Japan.
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
Genes, Nov. 2021, Reviewed, No invitation

Properties of new diffusion filters for treatment of amblyopia with accurate occlusive effects.
Sasaki Makoto, Iwasaki Tsuneto, Kondo Hiroyuki, Tawara Akihiko
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, Jun. 2016, Reviewed, No invitation

Novel mutations in the RS1 gene in Japanese patients with X-linked congenital retinoschisis.
Kondo Hiroyuki, Oku Kazuma, Katagiri Satoshi, Hayashi Takaaki, Nakano Tadashi, Iwata Akiko, Kuniyoshi Kazuki, Kusaka Shunji, Hiyoshi Atsushi, Uchio Eiichi, Kondo Mineo, Oishi Noriko, Kameya Shuhei, Mizota Atsushi, Naoi Nobuhisa, Ueno Shinji, Terasaki Hiroko, Morimoto Takeshi, Iwaki Masayoshi, Yoshitake Kazutoshi, Iejima Daisuke, Fujinami Kaoru, Tsunoda Kazushige, Shinoda Kei, Iwata Takeshi
Human genome variation, Jan. 2019, Reviewed, Null
Lead

Novel mutations in the COL2A1 gene in Japanese patients with Stickler syndrome.
Kondo Hiroyuki, Matsushita Itsuka, Nagata Tatsuo, Hayashi Takaaki, Kakinoki Masashi, Uchio Eiichi, Kondo Mineo, Ohji Masahito, Kusaka Shunji
Human genome variation, Jul. 2016, Reviewed, Null
Lead, Corresponding

Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing.
Suga Akiko, Yoshitake Kazutoshi, Minematsu Naoko, Tsunoda Kazushige, Fujinami Kaoru, Miyake Yozo, Kuniyoshi Kazuki, Hayashi Takaaki, Mizobuchi Kei, Ueno Shinji, Terasaki Hiroko, Kominami Taro, Nao-I Nobuhisa, Mawatari Go, Mizota Atsushi, Shinoda Kei, Kondo Mineo, Kato Kumiko, Sekiryu Tetsuju, Nakamura Makoto, Kusuhara Sentaro, Yamamoto Hiroyuki, Yamamoto Shuji, Mochizuki Kiyofumi, Kondo Hiroyuki, Matsushita Itsuka, Kameya Shuhei, 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
Human mutation, Dec. 2022, Null, Null

A Japanese Family With Autosomal Dominant Oculocutaneous Albinism Type 4.
Oki Ryoko, Yamada Kisaburo, Nakano Satoko, Kimoto Kenichi, Yamamoto Ken, Kondo Hiroyuki, Kubota Toshiaki
Investigative ophthalmology & visual science, Feb. 2017, Reviewed, Null

Safety and efficacy of ripasudil eye drops in preterm infants with retinopathy of prematurity: phase 1/2, open label, single-arm trial.
Arima Mitsuru, Inoue Hirosuke, Misumi Akiko, Tsukamoto Shoko, Matsushita Itsuka, Araki Shunsuke, Ohta Manami, Takahashi Kazumasa, Imazato Miyuki, Goto Tomoko, Aoki Yoshinori, Tagawa Koshiro, Hirose Masayuki, Fujita Yuito, Yoshida Noriko, Nakao Shintaro, Kondo Hiroyuki, Kusuhara Koichi, Kimura Kazuhiro, Hasegawa Shunji, Ikeda Yasuhiro, Kodama Yuki, Moritake Hiroshi, Ochiai Masayuki, Ohga Shouichi, Kishimoto Junji, Todaka Koji, Ieiri Ichiro, Sonoda Koh-Hei
Japanese journal of ophthalmology, Sep. 2024, Reviewed, No invitation

Measuring macular pigment optical density using reflective images of confocal scanning laser system.
Morita Hirofumi, Matsushita Itsuka, Fujino Yoshihisa, Obana Akira, Kondo Hiroyuki
Japanese journal of ophthalmology, Jan. 2024, Reviewed, Null
Last, Corresponding

Epidemiologic study of rhegmatogenous retinal detachment in Japan from the Diagnosis Procedure Combination database over a 2-year period (2014-2015).
Oku Kazuma, Tokutsu Kei, Matsuda Shinya, Kondo Hiroyuki
Japanese journal of ophthalmology, Nov. 2021, Reviewed, No invitation
Last, Corresponding

Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN.
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 of clinical medicine, May 2021, Reviewed, No invitation

Risk allele of the FZD4 gene for familial exudative vitreoretinopathy
Kondo Hiroyuki, Uchio Eiichi, Kusaka Shunji, Higasa Koichiro
Ophthalmic genetics, Apr. 2018, Reviewed, Null
Lead

Severe foveal hypoplasia and macular degeneration in Stickler syndrome caused by missense mutation in COL2A1 gene
Mamika Asano_x000D_ Katsuhiko Yokoyama_x000D_ Kazuma Oku_x000D_ Itsuka Matsushita_x000D_ Kenichi Kimoto_x000D_ Toshiaki Kubota_x000D_ Hiroyuki Kondo
Ophthalmic genetics, Apr. 2022, Reviewed, No invitation
Last, Corresponding

Familial exudative vitreoretinopathy with TGFBR2 mutation without signs of Loeys-Dietz syndrome.
Asano Toshiaki, Oku Kazuma, Kondo Hiroyuki
Ophthalmic genetics, Oct. 2021, Reviewed, No invitation
Last, Corresponding

Lack of FOXE3 coding mutation in a case of congenital aphakia.
Sano Yusuke, Matsukane Yusuke, Watanabe Akihisa, Sonoda Ko-Hei, Kondo Hiroyuki
Ophthalmic genetics, Dec. 2017, Reviewed, Null
Corresponding

Mutations in ATOH7 gene in patients with nonsyndromic congenital retinal nonattachment and familial exudative vitreoretinopathy.
Kondo Hiroyuki, Matsushita Itsuka, Tahira Tomoko, Uchio Eiichi, Kusaka Shunji
Ophthalmic genetics, Dec. 2016, Reviewed, No invitation
Lead, Corresponding

Corrigendum.
Kondo H
Ophthalmology, May 2018, Reviewed, Null
Lead

Foveal Hypoplasia in Patients with Stickler Syndrome.
Matsushita Itsuka, Nagata Tatsuo, Hayashi Takaaki, Kimoto Kenichi, Kubota Toshiaki, Ohji Masahito, Kusaka Shunji, Kondo Hiroyuki
Ophthalmology, Jun. 2017, Reviewed, Null
Corresponding

Familial Exudative Vitreoretinopathy With and Without Pathogenic Variants of Norrin/β-Catenin Signaling Genes.
Kondo Hiroyuki, Tsukahara-Kawamura Tomoko, Matsushita Itsuka, Nagata Tatsuo, Hayashi Takaaki, Nishina Sachiko, Higasa Koichiro, Uchio Eiichi, Kondo Mineo, Sakamoto Taiji, Kusaka Shunji
Ophthalmology science, 2024, Reviewed, Null
Lead

Angiographic Characteristics in Mild Familial Exudative Vitreoretinopathy with Genetically Confirmed Autosomal Dominant Inheritance.
Okamoto Misato, Matsushita Itsuka, Nagata Tatsuo, Fujino Yoshihisa, Kondo Hiroyuki
Ophthalmology. Retina, Feb. 2025, Reviewed, No invitation
Corresponding

Late Vitreoretinal Complications of Regressed Retinopathy of Prematurity: Retinal Break, Vitreous Hemorrhage, and Retinal Detachment.
Hsu Han-Tung, Yu-Chuan Kang Eugene, Blair Michael P, Shapiro Michael, Komati Rahul, Hubbard Baker G, Price Kenneth W, Capone Antonio, Drenser Kim A, Trese Michael T, Shields Ryan, Kondo Hiroyuki, Matsushita Itsuka, Yonekawa Yoshihiro, Patel Samir N, Kusaka Shunji, Mano Fukutaro, Olsen Karl R, Ells Anna, Amphornphruet Atchara, Walsh Mark K, Besirli Cagri G, Moinuddin Omar, Baumal Caroline R, Enriquez Ana Bety, Hwang Yih-Shiou, Lai Chi-Chun, Wu Wei-Chi
Ophthalmology. Retina, Mar. 2022, Null, Null

A PEDIATRIC CASE OF DISSEMINATED BARTONELLA HENSELAE INFECTION ACCOMPANIED BY MULTIPLE INTRACRANIAL LESIONS.
Hirakawa Jun, Kawamura Masaru, Hoshina Takayuki, Taniguchi Madoka, Kondo Hiroyuki, Satake Hiroshi, Nawata Aya, Tsuneoka Hidehiro, Kusuhara Koichi
The Pediatric infectious disease journal, Oct. 2023, Reviewed, Null

Correspondence
Todorich B，Thanos A，Yonekawa Y，Thomas B.j，Faia L.J，Chang E，Shulman J，Olsen K.R，Blair M.P，Shapiro M.P，Ferrone P，Vajzovic L，Toth C.A，Lee T.C，Robinson J，Hubbard B，Kondo H:
Retina, 2017, Reviewed, Null
Corresponding

ULTRA-WIDE FIELD FUNDUS AUTOFLUORESCENCE IMAGING OF EYES WITH STICKLER SYNDROME.
Fujimoto Kazushi, Nagata Tatsuo, Matsushita Itsuka, Oku Kazuma, Imagawa Mamika, Kuniyoshi Kazuki, Hayashi Takaaki, Kimoto Kenichi, Ohji Masahito, Kusaka Shunji, Kondo Hiroyuki
Retina (Philadelphia, Pa.), Mar. 2021, Reviewed, No invitation
Corresponding

Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing.
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
Scientific reports, May 2018, Reviewed, Null

Vitrectomy and external drainage of subretinal fluid containing high concentration of vascular endothelial growth factor for advanced coats disease.
Mano Fukutaro, Matsushita Itsuka, Kondo Hiroyuki, Utamura Shoko, Kondo Chiori, Kusaka Shunji
Scientific reports, Sep. 2021, Reviewed, No invitation

Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene.
Kondo Hiroyuki, Matsushita Itsuka, Nagata Tatsuo, Fujihara Etsuko, Hosono Katsuhiro, Uchio Eiichi, Hotta Yoshihiro, Kusaka Shunji
Translational vision science & technology, Jun. 2021, Reviewed, No invitation
Lead, Corresponding

Ergonomic aspects in the design of instrumentation for ophthalmic microsurgery
Marino Menozzi, Nadia Neumayer, Ying-Yin Huang, Akihisa Watanabe, Hideki Oyama, Goroh Fujimaki, _x000D_ Hiroyuki Kondo, Shin-ichi Izumi, Kageyu Noro
Zeitschrift für Arbeitswissenschaft, Mar. 2019, Reviewed, Null

Optical coherence tomography findings of the peripheral retina in patients with congenital X-linked retinoschisis.
Nakajima Ayaka, Kuniyoshi Kazuki, Iwahashi Chiharu, Mano Fukutaro, Hayashi Takaaki, Kondo Hiroyuki, Mizobuchi Kei, Matsushita Itsuka, Suga Akiko, Yoshitake Kazutoshi, Nakano Tadashi, Iwata Takeshi, Matsumoto Chota, Kusaka Shunji
Frontiers in medicine, 2023, Reviewed, Null

Color Functionality Used in Visual Display for Occupational and Environmental Safety and Managing Color Vision Deficiency.
Ochiai Nobuhisa, Kondo Hiroyuki
Journal of UOEH, Mar. 2017, Reviewed, Null

Efficacy and safety of rotigotine in elderly patients with Parkinson's disease in comparison with the non-elderly: a post hoc analysis of randomized, double-blind, placebo-controlled trials.
Nomoto Masahiro, Iwaki Hirotaka, Kondo Hiroyuki, Sakurai Masaya
Journal of neurology, Feb. 2018, Null, Null

EFFICACY OF INNER WALL RETINECTOMY FOR BULLOUS SCHISIS CAVITY HANGING OVER OR THREATENING THE MACULA IN PATIENTS WITH CONGENITAL X-LINKED RETINOSCHISIS.
Iwahashi Chiharu, Matsushita Itsuka, Kuniyoshi Kazuki, Kondo Hiroyuki, Kusaka Shunji
Retina (Philadelphia, Pa.), Jan. 2023, Reviewed, Null

OCULAR FEATURES ASSOCIATED WITH MUTATIONS IN ATOH7 GENE OVERLAP THOSE WITH FAMILIAL EXUDATIVE VITREORETINOPATHY.
Naruse Sho, Kondo Hiroyuki
Retinal cases & brief reports, Nov. 2023, Reviewed, Null
Last, Corresponding

小児の解剖学的な発達
近藤寛之, Single work
全日本病院出版, 2022

白色瞳孔　瘢痕期未熟児網膜症，その他の白色瞳孔
近藤寛之, Contributor
メジカルビュー社, Mar. 2016
9784758316231

網膜硝子体変性症　Stickler症候群，Wagner病，Goldmann-Favre病
近藤寛之, Contributor
メジカルビュー社, Mar. 2016
9784758316231

特集インタビュー　早期の予防治療、手術で未熟児網膜症に挑む
近藤　寛之, Single work
九州医事新報社, Apr. 2019

小児眼底疾患 Ⅰ.未熟児網膜症、Ⅱ.家族性滲出性硝子体網膜症、Ⅲ.黄斑ジストロフィー
近藤　寛之, Contributor
医学書院, Jan. 2019
9784260036504

VDT 作業による障害
近藤寛之, Contributor
医学書院, Jan. 2016
9784260023931

家族性滲出性硝子体網膜症
近藤寛之, Contributor
医学書院, Oct. 2016
9784260024792

Wagner症候群
近藤寛之, Contributor
医学書院, Oct. 2016
978-4-260-02479-2

Goldmann-Favre症候群
近藤寛之, Contributor
医学書院, Oct. 2016
9784260024792

Stickler症候群
近藤寛之, Contributor
医学書院, Oct. 2016
978-4-260-02479-2

Norrie病
近藤寛之, Contributor
医学書院, Oct. 2016
9784260024792

Ehlers-Danlos症候群
近藤寛之, Contributor
医学書院, Oct. 2016
978260024792

Bloch-Sulzberger症候群
近藤寛之, Contributor
医学書院, Oct. 2016
9784260024792

Bloch-sulzberger症候群
近藤寛之, Single work
医学書院, 2022

Stickler症候群
近藤寛之, Single work
医学書院, 2022

Goldmann-Favre症候群
近藤寛之, Single work
医学書院, 2022

小児の水晶体観察
近藤寛之, Single work
文光堂, 2022

未熟児網膜症
近藤寛之, Single work
文光堂, 2022

先天網膜分離症
近藤寛之, Contributor
文光堂, Apr. 2022

Wagner症候群
近藤寛之, Single work
医学書院, 2022

未熟児網膜症
近藤寛之, Single work
中山書店, 2024

16章　未熟児網膜症の基礎研究：遺伝子解析
近藤寛之, Contributor
三輪書店, Oct. 2018

17章　診断医迷う類似疾患：家族性滲出性硝子体網膜症
近藤寛之, Contributor
三輪書店, Oct. 2018
978-4-89590-643-2

遺伝性疾患-家族性滲出性硝子体網膜症
近藤寛之, Contributor
文光堂, Apr. 2017
9784830655494

遺伝性疾患-Stickler症候群
近藤寛之, Contributor
文光堂, Apr. 2017
9784830655494

その他の遺伝性硝子体疾患
近藤　寛之, Joint work
南江堂, Mar. 2019
9784524245475

家族性滲出性硝子体網膜症
近藤寛之, Single work
南江堂, 2022

網膜硝子体変性-Stickler症候群、Wagner症候群
近藤寛之, Contributor
医学書院, Nov. 2016
9784260028011

網膜硝子体変性-家族性滲出性硝子体網膜症
近藤寛之, Contributor
医学書院, Nov. 2016
9784260028011

Stickler症候群,Wagner病
近藤寛之, Single work
文光堂, 2024

家族性滲出性硝子体網膜症（FEVR)
近藤寛之, Single work
中山書店, 2024

乳児・小児の眼底疾患、未熟児網膜症
近藤寛之, Contributor
メジカルビュー社, Jan. 2017
9784758316279

小児の網膜レーザー治療、硝子体手術
近藤寛之, Contributor
メジカルビュー社, Mar. 2017
9784758316286

Genetic testing in pediatric retina
Hiroyuki Kondo, Joint work
Springer Nature Singapore, 2021
978-981-15-6551-9