Research keywords (4):
Retina
, Electrophysiology of vision
, Hereditary chorioretinal dystrophy
, Retinopahty of Prematurity
Research theme for competitive and other funds (6):
2022 - 2025 遺伝性網膜・視神経ジストロフィの症例収拾および疾患別頻度の検討
2020 - 2025 未熟児網膜症における増殖膜線維化の病態解明
2018 - 2022 Development of glaucoma regeneration treatment method by intraretinal remodeling phenomenon
2017 - 2020 Anti-VEGF treatment for severe retinopathy of prematurity
2014 - 2017 The role of periostin in the pathogenesis of retinopathy of prematurity (ROP) and the effect of 2 anti-vascular endothelial growth factors in the treatment of ROP
2011 - 2013 Studies on the pathogenesis and anti-VEGF treatment of retinopathy of prematurity
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Papers (120):
Tomoko Sato, Kazuki Kuniyoshi, Takaaki Hayashi, Hirokazu Nishiwaki, Kei Mizobuchi, Shunji Kusaka. Clinical course of two siblings with potassium voltage-gated channel modifier subfamily V member 2 (KCNV2)-associated retinopathy. Documenta ophthalmologica. Advances in ophthalmology. 2024
Kei Mizobuchi, Takaaki Hayashi, Koji Tanaka, Kazuki Kuniyoshi, Yusuke Murakami, Natsuko Nakamura, Kaoruko Torii, Atsushi Mizota, Daiki Sakai, Akiko Maeda, et al. Genetic and clinical features of ABCA4-associated retinopathy in a Japanese nationwide cohort. American journal of ophthalmology. 2024
Akiko Suga, Kei Mizobuchi, Taiga Inooka, Kazutoshi Yoshitake, Naoko Minematsu, Kazushige Tsunoda, Kazuki Kuniyoshi, Yosuke Kawai, Yosuke Omae, Katsushi Tokunaga, et al. A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD. Genetics in Medicine Open. 2024. 101843-101843