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RP2-associated retinal disorder in a Japanese cohort: Report of novel variants and a literature review, identifying a genotype-phenotype association.
Fujinami K, Liu X, Ueno S, Mizota A, Shinoda K, Kuniyoshi K, Fujinami-Yokokawa Y, Yang L, Arno G, Pontikos N, Kameya S, Kominami T, Terasaki H, Sakuramoto H, Nakamura N, Kurihara T, Tsubota K, Miyake Y, Yoshiake K, Iwata T, Tsunoda K; Japan Eye Genetics Consortium Study Group. Fujinami K, et al. Among authors: shinoda k. Am J Med Genet C Semin Med Genet. 2020 Sep;184(3):675-693. doi: 10.1002/ajmg.c.31830. Epub 2020 Sep 1. Am J Med Genet C Semin Med Genet. 2020. PMID: 32875684
Transient macular dysfunction determined by focal macular electroretinogram.
Terauchi N, Fujinami K, Shinoda K, Tsunoda K, Hanazono G, Miyake Y, Inomata K. Terauchi N, et al. Among authors: shinoda k. Br J Ophthalmol. 2007 Dec;91(12):1709-10. doi: 10.1136/bjo.2006.113373. Br J Ophthalmol. 2007. PMID: 18024815 Free PMC article. No abstract available.
Retinal dysfunction and progressive retinal cell death in SOD1-deficient mice.
Hashizume K, Hirasawa M, Imamura Y, Noda S, Shimizu T, Shinoda K, Kurihara T, Noda K, Ozawa Y, Ishida S, Miyake Y, Shirasawa T, Tsubota K. Hashizume K, et al. Among authors: shinoda k. Am J Pathol. 2008 May;172(5):1325-31. doi: 10.2353/ajpath.2008.070730. Epub 2008 Mar 27. Am J Pathol. 2008. PMID: 18372426 Free PMC article.
867 results