2024年
原著論文
- Ueno S, Hayashi T, Tsunoda K, Aoki T, Kondo M.
Nationwide epidemiologic survey on incidence of macular dystrophy in Japan
Jpn J Ophthalmol. 2024 Apr 3.
- Goto K, Koyanagi Y, Akiyama M, Murakami Y, Fukushima M, Fujiwara K, Iijima H, Yamaguchi M, Endo M, Hashimoto K, Ishizu M, Hirakata T, Mizobuchi K, Takayama M, Ota J, Sajiki AF, Kominami T, Ushida H, Fujita K, Kaneko H, Ueno S, Hayashi T, Terao C, Hotta Y, Murakami A, Kuniyoshi K, Kusaka S, Wada Y, Abe T, Nakazawa T, Ikeda Y, Momozawa Y, Sonoda KH, Nishiguchi KM.
Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseases
J Med Genet. 2024 Mar 18:jmg-2023-109750.
- Mizobuchi K, Hayashi T, Tanaka K, Kuniyoshi K, Murakami Y, Nakamura N, Torii K, Mizota A, Sakai D, Maeda A, Kominami T, Ueno S, Kusaka S, Nishiguchi KM, Ikeda Y, Kondo M, Tsunoda K, Hotta Y, Nakano T.
Genetic and clinical features of ABCA4-associated retinopathy in a Japanese nationwide cohort
Am J Ophthalmol. 2024 Mar 16:S0002-9394(24)00110-7.
- Watanabe T, Takihara Y, Jono H, Fujimoto T, Tasaki M, Isoguchi A, Urahashi Y, Shimoda T, Takahashi E, Ando Y, Ueno S, Ueda M, Inoue T.
Silencing of ocular transthyretin, a gene responsible for hereditary transthyretin amyloidosis, by intravitreal injection of an siRNA conjugate into rabbit eyes.
Biochem Biophys Res Commun. 2024 Jan 29;694:149397.
Copyright © 2022 Department of Ophthalmogy, Hirosaki University School of Medicine.