Autosomal dominant foveal hypoplasia without visible macular abnormalities and PAX6 mutations
Matsushita, Itsuka, Morita, Hirofumi, Kondo, Hiroyuki
Published in Japanese journal of ophthalmology (01.11.2020)
Published in Japanese journal of ophthalmology (01.11.2020)
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Journal Article
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
Published in Scientific reports (29.09.2021)
Published in Scientific reports (29.09.2021)
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Journal Article
Foveal Hypoplasia in Patients with Stickler Syndrome
Matsushita, Itsuka, MD, Nagata, Tatsuo, MD, PhD, Hayashi, Takaaki, MD, PhD, Kimoto, Kenichi, MD, PhD, Kubota, Toshiaki, MD, PhD, Ohji, Masahito, MD, PhD, Kusaka, Shunji, MD, PhD, Kondo, Hiroyuki, MD, PhD
Published in Ophthalmology (Rochester, Minn.) (01.06.2017)
Published in Ophthalmology (Rochester, Minn.) (01.06.2017)
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Journal Article
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
Published in Documenta ophthalmologica (01.12.2021)
Published in Documenta ophthalmologica (01.12.2021)
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Journal Article
Electroretinograms of eyes with Stickler syndrome
Kondo, Hiroyuki, Fujimoto, Kazushi, Imagawa, Mamika, Oku, Kazuma, Matsushita, Itsuka, Hayashi, Takaaki, Nagata, Tatsuo
Published in Documenta ophthalmologica (01.06.2020)
Published in Documenta ophthalmologica (01.06.2020)
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Journal Article
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
Published in Japanese journal of ophthalmology (01.09.2024)
Published in Japanese journal of ophthalmology (01.09.2024)
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Journal Article
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
Published in Frontiers in medicine (16.11.2023)
Published in Frontiers in medicine (16.11.2023)
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Journal Article
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
Published in BMJ open (27.07.2021)
Published in BMJ open (27.07.2021)
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Journal Article
Severe foveal hypoplasia and macular degeneration in Stickler syndrome caused by missense mutation in COL2A1 gene
Asano, Mamika, Yokoyama, Katsuhiko, Oku, Kazuma, Matsushita, Itsuka, Kimoto, Kenichi, Kubota, Toshiaki, Kondo, Hiroyuki
Published in Ophthalmic genetics (04.07.2022)
Published in Ophthalmic genetics (04.07.2022)
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Journal Article
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
Published in Retina (Philadelphia, Pa.) (01.01.2023)
Published in Retina (Philadelphia, Pa.) (01.01.2023)
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Journal Article
Angiographic Characteristics in Mild Familial Exudative Vitreoretinopathy with Genetically Confirmed Autosomal Dominant Inheritance
Okamoto, Misato, Matsushita, Itsuka, Nagata, Tatsuo, Fujino, Yoshihisa, Kondo, Hiroyuki
Published in Ophthalmology retina (27.08.2024)
Published in Ophthalmology retina (27.08.2024)
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Journal Article
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
Published in European journal of human genetics : EJHG (01.04.2024)
Published in European journal of human genetics : EJHG (01.04.2024)
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Journal Article
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Iwahashi, Chiharu, Matsushita, Itsuka, Kuniyoshi, Kazuki, Kondo, Hiroyuki, Kusaka, Shunji
Published in Retina (Philadelphia, Pa.) (01.07.2023)
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Published in Retina (Philadelphia, Pa.) (01.07.2023)
Journal Article
Severe foveal hypoplasia and macular degeneration in Stickler syndrome caused by missense mutation in COL2A1 gene
Asano, Mamika, Yokoyama, Katsuhiko, Oku, Kazuma, Matsushita, Itsuka, Kimoto, Kenichi, Kubota, Toshiaki, Kondo, Hiroyuki
Published in Ophthalmic genetics (01.08.2022)
Published in Ophthalmic genetics (01.08.2022)
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Journal Article
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
Published in Genes (21.07.2023)
Published in Genes (21.07.2023)
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Journal Article
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
Published in Retina (Philadelphia, Pa.) (01.03.2021)
Published in Retina (Philadelphia, Pa.) (01.03.2021)
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Journal Article
Functional Characteristics of Diverse IPAX6/I Mutations Associated with Isolated Foveal Hypoplasia
Matsushita, Itsuka, Izumi, Hiroto, Ueno, Shinji, Hayashi, Takaaki, Fujinami, Kaoru, Tsunoda, Kazushige, Iwata, Takeshi, Kiuchi, Yoshiaki, Kondo, Hiroyuki
Published in Genes (01.07.2023)
Published in Genes (01.07.2023)
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Journal Article
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
Published in Human mutation (01.12.2022)
Published in Human mutation (01.12.2022)
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