Detailed Morphological Changes of Foveoschisis in Patient with X-Linked Retinoschisis Detected by SD-OCT and Adaptive Optics Fundus Camera

door Akeo, Keiichiro, Kameya, Shuhei, Gocho, Kiyoko, Kubota, Daiki, Yamaki, Kunihiko, Takahashi, Hiroshi
Gepubliceerd in Case Rep Ophthalmol Med (2015)

The first Japanese family of CDH3‐related hypotrichosis with juvenile macular dystrophy

door Hayashi, Takaaki, Katagiri, Satoshi, Kubota, Daiki, Mizobuchi, Kei, Ishiuji, Yozo, Asahina, Akihiko, Kameya, Shuhei, Nakano, Tadashi
Gepubliceerd in Mol Genet Genomic Med (2021)

Genetic defects of CHM and visual acuity outcome in 24 choroideremia patients from 16 Japanese families

door Hayashi, Takaaki, Kameya, Shuhei, Mizobuchi, Kei, Kubota, Daiki, Kikuchi, Sachiko, Yoshitake, Kazutoshi, Mizota, Atsushi, Murakami, Akira, Iwata, Takeshi, Nakano, Tadashi
Gepubliceerd in Sci Rep (2020)

Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation

door Kubota, Daiki, Gocho, Kiyoko, Akeo, Keiichiro, Kikuchi, Sachiko, Sugahara, Michitaka, Matsumoto, Celso Soiti, Shinoda, Kei, Mizota, Atsushi, Yamaki, Kunihiko, Takahashi, Hiroshi, Kameya, Shuhei
Gepubliceerd in Doc Ophthalmol (2016)

Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with DRAM2-Associated Retinopathy

door Kuniyoshi, Kazuki, Hayashi, Takaaki, Kameya, Shuhei, Katagiri, Satoshi, Mizobuchi, Kei, Tachibana, Toshiaki, Kubota, Daiki, Sakuramoto, Hiroyuki, Tsunoda, Kazushige, Fujinami, Kaoru, Yoshitake, Kazutoshi, Iwata, Takeshi, Nakano, Tadashi, Kusaka, Shunji
Gepubliceerd in Int J Mol Sci (2020)

Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN

door 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
Gepubliceerd in J Clin Med (2021)