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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

ROP長期経過観察のポイント（特集 未熟児網膜症アップデート）
松下五佳
日本の眼科, Oct. 2022, Not reviewed, Null
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

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
Lead

【未熟児網膜症アップデート】未熟児網膜症のリハビリテーション・ロービジョンケア
松下 五佳
眼科, Jan. 2023, Null, Null
Lead

小児のロービジョンケア
村上　美紀、松下　五佳
眼科グラフィック, Dec. 2019, Reviewed, Null

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

【眼科の処置・小手術・最新の治療-基本手技から緊急時の対応まで】小児眼科・斜視　未熟児網膜症に対する治療
松下 五佳
臨床眼科, Oct. 2023, Not reviewed, No invitation
Lead

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

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
Lead

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

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

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

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

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

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

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

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

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

Norrie病
松下五佳, Single work
医学書院, Sep. 2022

眼科領域-小児の眼外傷
松下　五佳, Joint work
東京医学社, Nov. 2019

黄斑低形成
松下五佳, Single work
文光堂, 2023

各論1.網膜 1)先天・発育異常 (8)黄斑低形成_x000D_ 各論4.視神経 1)先天異常 (1)乳頭欠損，無形性
松下　五佳, Joint work
総合医学社, Oct. 2019
9784883786862

松下五佳, Single work
南江堂, 2024

松下五佳, Single work
中山書店, 2024

黄斑低形成
松下五佳, Single work
中山書店, 2023

未熟児網膜症に対する治療
松下五佳, Single work
医学書院, 2023