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Documenta Ophthalmologica. Advances in Ophthalmology|July 11, 2020
Progress of macular atrophy during 30 months' follow-up in a patient with spinocerebellar ataxia type1 (SCA1)Ayane Hirose, Satoshi Katagiri, Takaaki Hayashi, et al.
Molecular Genetics & Genomic Medicine|May 23, 2020
Novel homozygous CLN3 missense variant in isolated retinal dystrophy: A case report and electron microscopic findingsKei Mizobuchi, Takaaki Hayashi, Kazutoshi Yoshitake, et al.
Acta Crystallographica. Section D, Biological Crystallography|February 22, 2003
Expression, purification and preliminary crystallographic analysis of human sorbitol dehydrogenaseConnie Darmanin, Takeshi Iwata, Deborah A Carper, et al.
Biomed Research International|September 9, 2014
Pattern visual evoked potentials elicited by organic electroluminescence screenCelso Soiti Matsumoto, Kei Shinoda, Harue Matsumoto, et al.
Plos One|February 25, 2011
Modeling retinal degeneration using patient-specific induced pluripotent stem cellsZi-Bing Jin, Satoshi Okamoto, Fumitaka Osakada, et al.
Investigative Ophthalmology & Visual Science|January 26, 2007
Proteomic and transcriptomic analyses of retinal pigment epithelial cells exposed to REF-1/TFPI-2Masahiko Shibuya, Haru Okamoto, Takehiro Nozawa, et al.
Human Molecular Genetics|July 16, 2010
Mutant WDR36 directly affects axon growth of retinal ganglion cells leading to progressive retinal degeneration in miceZai-Long Chi, Fumie Yasumoto, Yuri Sergeev, et al.
The British Journal of Ophthalmology|July 24, 2015
Mutation analysis of BEST1 in Japanese patients with Best's vitelliform macular dystrophySatoshi Katagiri, Takaaki Hayashi, Yasuhiro Ohkuma, et al.
Acta Ophthalmologica|August 19, 2014
Lack of association of LOXL1 gene variants in Japanese patients with central retinal vein occlusion without clinically detectable pseudoexfoliation material depositsMasaki Tanito, Katsunori Hara, Masakazu Akahori, et al.
Ophthalmic Genetics|January 14, 2022
Clinical course of a Japanese girl with Leber congenital amaurosis associated with a novel nonsense pathogenic variant in NMNAT1: a case report and mini reviewTomoyasu Kayazawa, Kazuki Kuniyoshi, Yoshikazu Hatsukawa, et al.
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