Optical coherence tomography and video recording of a case of bilateral contractile peripapillary staphyloma

por Yoshida, Tomoyo, Katagiri, Satoshi, Yokoi, Tadashi, Nishina, Sachiko, Azuma, Noriyuki
Publicado 2018

Atypical intravitreal growth of retinoblastoma with a multi-branching configuration

por Nishina, Sachiko, Katagiri, Satoshi, Nakazawa, Atsuko, Kiyotani, Chikako, Yokoi, Tadashi, Azuma, Noriyuki
Publicado 2017

Generation of retinal ganglion cells with functional axons from human induced pluripotent stem cells

por Tanaka, Taku, Yokoi, Tadashi, Tamalu, Fuminobu, Watanabe, Shu-Ichi, Nishina, Sachiko, Azuma, Noriyuki
Publicado 2015

Genotype–phenotype correlation of PAX6 gene mutations in aniridia

por Yokoi, Tadashi, Nishina, Sachiko, Fukami, Maki, Ogata, Tsutomu, Hosono, Katsuhiro, Hotta, Yoshihiro, Azuma, Noriyuki
Publicado 2016

Electroretinographic effects of retinal dragging and retinal folds in eyes with familial exudative vitreoretinopathy

por Yaguchi, Yukari, Katagiri, Satoshi, Fukushima, Yoko, Yokoi, Tadashi, Nishina, Sachiko, Kondo, Mineo, Azuma, Noriyuki
Publicado 2016

Retinal Structure and Function in Eyes with Optic Nerve Hypoplasia

por Katagiri, Satoshi, Nishina, Sachiko, Yokoi, Tadashi, Mikami, Masashi, Nakayama, Yuri, Tanaka, Michiko, Azuma, Noriyuki
Publicado 2017

Effects of neuroactive agents on axonal growth and pathfinding of retinal ganglion cells generated from human stem cells

por Yokoi, Tadashi, Tanaka, Taku, Matsuzaka, Emiko, Tamalu, Fuminobu, Watanabe, Shu-Ichi, Nishina, Sachiko, Azuma, Noriyuki
Publicado 2017

Retinal structure in Leber’s congenital amaurosis caused by RPGRIP1 mutations

por Miyamichi, Daisuke, Nishina, Sachiko, Hosono, Katsuhiro, Yokoi, Tadashi, Kurata, Kentaro, Sato, Miho, Hotta, Yoshihiro, Azuma, Noriyuki
Publicado 2019

X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers

por Kurata, Kentaro, Hosono, Katsuhiro, Hayashi, Takaaki, Mizobuchi, Kei, Katagiri, Satoshi, Miyamichi, Daisuke, Nishina, Sachiko, Sato, Miho, Azuma, Noriyuki, Nakano, Tadashi, Hotta, Yoshihiro
Publicado 2019

Clinical features of a toddler with bilateral bullous retinoschisis with a novel RS1 mutation

por Katagiri, Satoshi, Tanaka, Shin, Yokoi, Tadashi, Hayashi, Takaaki, Matsuzaka, Emiko, Ueda, Kazuko, Yoshida-Uemura, Tomoyo, Arakawa, Akira, Nishina, Sachiko, Kadonosono, Kazuaki, Azuma, Noriyuki
Publicado 2016

A pediatric case of congenital stromal corneal dystrophy caused by the novel variant c.953del of the DCN gene

por Morikawa, Hazuki, Nishina, Sachiko, Torii, Kaoruko, Hosono, Katsuhiro, Yokoi, Tadashi, Shigeyasu, Chika, Yamada, Masakazu, Kosuga, Motomichi, Fukami, Maki, Saitsu, Hirotomo, Azuma, Noriyuki, Hori, Yuichi, Hotta, Yoshihiro
Publicado 2023

Biallelic CDK9 variants as a cause of a new multiple-malformation syndrome with retinal dystrophy mimicking the CHARGE syndrome

por Nishina, Sachiko, Hosono, Katsuhiro, Ishitani, Shizuka, Kosaki, Kenjiro, Yokoi, Tadashi, Yoshida, Tomoyo, Tomita, Kaoru, Fukami, Maki, Saitsu, Hirotomo, Ogata, Tsutomu, Ishitani, Tohru, Hotta, Yoshihiro, Azuma, Noriyuki
Publicado 2021

The Structural Abnormalities Are Deeply Involved in the Cause of RPGRIP1-Related Retinal Dystrophy in Japanese Patients

por Torii, Kaoruko, Nishina, Sachiko, Morikawa, Hazuki, Mizobuchi, Kei, Takayama, Masakazu, Tachibana, Nobutaka, Kurata, Kentaro, Hikoya, Akiko, Sato, Miho, Nakano, Tadashi, Fukami, Maki, Azuma, Noriyuki, Hayashi, Takaaki, Saitsu, Hirotomo, Hotta, Yoshihiro
Publicado 2023

Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa

por Tachibana, Nobutaka, Hosono, Katsuhiro, Nomura, Shuhei, Arai, Shinji, Torii, Kaoruko, Kurata, Kentaro, Sato, Miho, Shimakawa, Shuichi, Azuma, Noriyuki, Ogata, Tsutomu, Wada, Yoshinao, Okamoto, Nobuhiko, Saitsu, Hirotomo, Nishina, Sachiko, Hotta, Yoshihiro
Publicado 2022

Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing

por 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
Publicado 2018

The clock components Period2, Cryptochrome1a, and Cryptochrome2a function in establishing light-dependent behavioral rhythms and/or total activity levels in zebrafish

por Hirayama, Jun, Alifu, Yikelamu, Hamabe, Rin, Yamaguchi, Sho, Tomita, Jun, Maruyama, Yusuke, Asaoka, Yoichi, Nakahama, Ken-ichi, Tamaru, Teruya, Takamatsu, Ken, Takamatsu, Nobuhiko, Hattori, Atsuhiko, Nishina, Sachiko, Azuma, Noriyuki, Kawahara, Atsuo, Kume, Kazuhiko, Nishina, Hiroshi
Publicado 2019

The mevalonate pathway regulates primitive streak formation via protein farnesylation

por Okamoto-Uchida, Yoshimi, Yu, Ruoxing, Miyamura, Norio, Arima, Norie, Ishigami-Yuasa, Mari, Kagechika, Hiroyuki, Yoshida, Suguru, Hosoya, Takamitsu, Nawa, Makiko, Kasama, Takeshi, Asaoka, Yoichi, Alois, Reiner Wimmer, Elling, Ulrich, Penninger, Josef M., Nishina, Sachiko, Azuma, Noriyuki, Nishina, Hiroshi
Publicado 2016

Two Novel Mutations in the EYS Gene Are Possible Major Causes of Autosomal Recessive Retinitis Pigmentosa in the Japanese Population

por Hosono, Katsuhiro, Ishigami, Chie, Takahashi, Masayo, Park, Dong Ho, Hirami, Yasuhiko, Nakanishi, Hiroshi, Ueno, Shinji, Yokoi, Tadashi, Hikoya, Akiko, Fujita, Taichi, Zhao, Yang, Nishina, Sachiko, Shin, Jae Pil, Kim, In Taek, Yamamoto, Shuichi, Azuma, Noriyuki, Terasaki, Hiroko, Sato, Miho, Kondo, Mineo, Minoshima, Shinsei, Hotta, Yoshihiro
Publicado 2012