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Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseases.
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. Goto K, et al. Among authors: kusaka s. J Med Genet. 2024 Jun 20;61(7):613-620. doi: 10.1136/jmg-2023-109750. J Med Genet. 2024. PMID: 38499336
Intravitreal injection of bevacizumab for retinopathy of prematurity.
Kuniyoshi K, Sugioka K, Sakuramoto H, Kusaka S, Wada N, Shimomura Y. Kuniyoshi K, et al. Among authors: kusaka s. Jpn J Ophthalmol. 2014 May;58(3):237-43. doi: 10.1007/s10384-014-0310-z. Epub 2014 Feb 26. Jpn J Ophthalmol. 2014. PMID: 24566819
Identification of vitreous proteins in retinopathy of prematurity.
Sugioka K, Saito A, Kusaka S, Kuniyoshi K, Shimomura Y. Sugioka K, et al. Among authors: kusaka s. Biochem Biophys Res Commun. 2017 Jul 1;488(3):483-488. doi: 10.1016/j.bbrc.2017.05.067. Epub 2017 May 11. Biochem Biophys Res Commun. 2017. PMID: 28502635
Novel mutations in the RS1 gene in Japanese patients with X-linked congenital retinoschisis.
Kondo H, Oku K, Katagiri S, Hayashi T, Nakano T, Iwata A, Kuniyoshi K, Kusaka S, Hiyoshi A, Uchio E, Kondo M, Oishi N, Kameya S, Mizota A, Naoi N, Ueno S, Terasaki H, Morimoto T, Iwaki M, Yoshitake K, Iejima D, Fujinami K, Tsunoda K, Shinoda K, Iwata T. Kondo H, et al. Among authors: kusaka s. Hum Genome Var. 2019 Jan 8;6:3. doi: 10.1038/s41439-018-0034-6. eCollection 2019. Hum Genome Var. 2019. PMID: 30652005 Free PMC article.
370 results