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

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

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

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

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

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

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

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

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

Yazar: 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
Yayımlandı Int J Mol Sci (2020)

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

Yazar: 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
Yayımlandı J Clin Med (2021)