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

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

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

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

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

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

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

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

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

Tekijä 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
Julkaisussa Int J Mol Sci (2020)

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

Tekijä 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
Julkaisussa J Clin Med (2021)