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Motokazu Tsujikawa

Osaka University

180

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3999

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A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa.

2021
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Drug screening with zebrafish visual behavior identifies carvedilol as a potential treatment for an autosomal dominant form of retinitis pigmentosa.

2021 Scientific Reports
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Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese.

2020 Clinical and Experimental Ophthalmology
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Identification of TIE2 as a susceptibility gene for neovascular age-related macular degeneration and polypoidal choroidal vasculopathy

2020 British Journal of Ophthalmology
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27-year follow-up of Japanese siblings with juvenile cone rod dystrophy 13 due to a novel RPGRIP1 gene mutation

2020 Investigative Ophthalmology & Visual Science
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Choroidal Neovascularization Associated with Morning Glory Syndrome: A Case Report

2020
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Quantitative Analysis of the Association Between Follow-Up Duration and Severity of Limbal Stem Cell Deficiency or Visual Acuity in Aniridia.

2020 Investigative Ophthalmology & Visual Science
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Novel mutation identified in Leber congenital amaurosis - a case report.

2020 BMC Ophthalmology
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The effect of PCR testing on the clinical course in herpetic uveitis

2019 Investigative Ophthalmology & Visual Science
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A novel mutation in gelatinous drop-like corneal dystrophy and functional analysis

2019 Human genome variation
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