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Case Reports in Ophthalmological Medicine|September 11, 2015
Detailed Morphological Changes of Foveoschisis in Patient with X-Linked Retinoschisis Detected by SD-OCT and Adaptive Optics Fundus CameraKeiichiro Akeo, Shuhei Kameya, Kiyoko Gocho, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|February 20, 2025
Relatively preserved retinal function in RPE65-associated retinopathy: a case reportKei Mizobuchi, Takaaki Hayashi, Shuhei Kameya, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|May 25, 2023
A mild form of POC1B-associated retinal dystrophy with relatively preserved cone system functionTakaaki Hayashi, Kei Mizobuchi, Shuhei Kameya, et al.
Case Reports in Ophthalmological Medicine|February 12, 2021
Optical Coherence Tomography Angiography of Nonarteritic Cilioretinal Artery Occlusion AloneToyo Ikebukuro, Tsutomu Igarashi, Shuhei Kameya, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|February 21, 2021
A new PDE6A missense variant p.Arg544Gln in rod-cone dystrophyTakaaki Hayashi, Kei Mizobuchi, Shuhei Kameya, et al.
Medicine|July 19, 2024
Multimodal imaging analysis of autosomal recessive bestrophinopathy: Case seriesMasahiro Miura, Shuichi Makita, Yoshiaki Yasuno, et al.
Japanese Journal of Ophthalmology|July 3, 2017
Heterozygous deletion of the OPA1 gene in patients with dominant optic atrophyTakaaki Hayashi, Hiroyuki Sasano, Satoshi Katagiri, et al.
Molecular Genetics & Genomic Medicine|April 10, 2021
The first Japanese family of CDH3-related hypotrichosis with juvenile macular dystrophyTakaaki Hayashi, Satoshi Katagiri, Daiki Kubota, et al.
Human Molecular Genetics|July 26, 2002
Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6Shuhei Kameya, Norman L Hawes, Bo Chang, et al.
Biomed Research International|December 27, 2013
High-resolution en face images of microcystic macular edema in patients with autosomal dominant optic atrophyKiyoko Gocho, Sachiko Kikuchi, Takenori Kabuto, et al.
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