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Seminars in Ophthalmology|July 6, 2017
Visual Outcomes in Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A MutationsYasunori Nagase, Kentaro Kurata, Katsuhiro Hosono, et al.
Journal of Human Genetics|September 15, 2025
Novel biallelic CDK9 variants are associated with retinal dystrophy without CHARGE-like malformation syndromeSachiko Nishina, Kaoruko Torii, Shizuka Ishitani, et al.
Biological & Pharmaceutical Bulletin|March 5, 2011
Protective effects of cyclo(L-Leu-L-Tyr) against postischemic myocardial dysfunction in guinea-pig heartsKumiko Mitsui-Saitoh, Tadashi Furukawa, Takashi Akutagawa, et al.
Japanese Journal of Ophthalmology|April 19, 2022
Exophthalmos associated with chronic progressive external ophthalmoplegiaYu Takeda, Hiroko Suzuki, Katsuhiro Hosono, et al.
Journal of Human Genetics|May 27, 2016
Novel HPS6 mutations identified by whole-exome sequencing in two Japanese sisters with suspected ocular albinismDaisuke Miyamichi, Miki Asahina, Junya Nakajima, et al.
Ophthalmic Genetics|February 21, 2013
Clinical phenotype in ten unrelated Japanese patients with mutations in the EYS geneKimiko Suto, Katsuhiro Hosono, Masayo Takahashi, et al.
International Journal of Molecular Sciences|March 29, 2019
X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female CarriersKentaro Kurata, Katsuhiro Hosono, Takaaki Hayashi, et al.
Ophthalmic Genetics|November 7, 2022
A case of siblings with juvenile retinitis pigmentosa associated with NEK1 gene variantsAkiko Hikoya, Katsuhiro Hosono, Kaoru Ono, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 31, 2020
Novel biallelic splice-site BBS1 variants in Bardet-Biedle syndrome: a case report of the first Japanese patientSatoshi Katagiri, Katsuhiro Hosono, Takaaki Hayashi, et al.
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