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Missense mutation of NRAS is associated with malignant progression in neurocutaneous melanosis.
Takahashi H, Natsumeda M, Hara N, Koyama A, Shimizu H, Miyashita A, Satake D, Mouri Y, Tsukano J, Kawabe K, Tsukamoto Y, Okada M, Ogura R, Yuki A, Umezu H, Kakita A, Ikeuchi T, Oishi M. Takahashi H, et al. Among authors: hara n. Acta Neuropathol Commun. 2024 Jan 22;12(1):14. doi: 10.1186/s40478-024-01723-0. Acta Neuropathol Commun. 2024. PMID: 38254245 Free PMC article.
Oculopharyngodistal myopathy with coexisting histology of systemic neuronal intranuclear inclusion disease: Clinicopathologic features of an autopsied patient harboring CGG repeat expansions in LRP12.
Saito R, Shimizu H, Miura T, Hara N, Mezaki N, Higuchi Y, Miyashita A, Kawachi I, Sanpei K, Honma Y, Onodera O, Ikeuchi T, Kakita A. Saito R, et al. Among authors: hara n. Acta Neuropathol Commun. 2020 Jun 3;8(1):75. doi: 10.1186/s40478-020-00945-2. Acta Neuropathol Commun. 2020. PMID: 32493488 Free PMC article. No abstract available.
Clinicopathologic features of two unrelated autopsied patients with Charcot-Marie-Tooth disease carrying MFN2 gene mutation.
Hayashi H, Saito R, Tanaka H, Hara N, Koide S, Yonemochi Y, Ozawa T, Hokari M, Toyoshima Y, Miyashita A, Onodera O, Okamoto K, Ikeuchi T, Nakajima T, Kakita A. Hayashi H, et al. Among authors: hara n. Acta Neuropathol Commun. 2023 Dec 20;11(1):207. doi: 10.1186/s40478-023-01692-w. Acta Neuropathol Commun. 2023. PMID: 38124143 Free PMC article. No abstract available.
Genetics of Alzheimer's disease: an East Asian perspective.
Miyashita A, Kikuchi M, Hara N, Ikeuchi T. Miyashita A, et al. Among authors: hara n. J Hum Genet. 2023 Mar;68(3):115-124. doi: 10.1038/s10038-022-01050-z. Epub 2022 Jun 1. J Hum Genet. 2023. PMID: 35641666 Free PMC article. Review.
1,092 results