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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. 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.
A patient clinically diagnosed as multiple system atrophy harboring LRRK2 p.G2019S.
Ando S, Konno T, Ishihara T, Hayashi H, Saito N, Nishioka K, Hattori N, Wszolek ZK, Onodera O. Ando S, et al. Among authors: hayashi h. Clin Park Relat Disord. 2019 Nov 16;1:100-101. doi: 10.1016/j.prdoa.2019.11.002. eCollection 2019. Clin Park Relat Disord. 2019. PMID: 34316610 Free PMC article. No abstract available.
[Rethinking Lacunar Stroke: Beyond Fisher's Curse].
Onodera O, Uemura M, Ando S, Hayashi H, Kanazawa M. Onodera O, et al. Among authors: hayashi h. Brain Nerve. 2021 Sep;73(9):991-998. doi: 10.11477/mf.1416201876. Brain Nerve. 2021. PMID: 34462370 Japanese.
Heterogenous Genetic, Clinical, and Imaging Features in Patients with Neuronal Intranuclear Inclusion Disease Carrying NOTCH2NLC Repeat Expansion.
Fitrah YA, Higuchi Y, Hara N, Tokutake T, Kanazawa M, Sanpei K, Taneda T, Nakajima A, Koide S, Tsuboguchi S, Watanabe M, Fukumoto J, Ando S, Sato T, Iwafuchi Y, Sato A, Hayashi H, Ishiguro T, Takeda H, Takahashi T, Fukuhara N, Kasuga K, Miyashita A, Onodera O, Ikeuchi T. Fitrah YA, et al. Among authors: hayashi h. Brain Sci. 2023 Jun 15;13(6):955. doi: 10.3390/brainsci13060955. Brain Sci. 2023. PMID: 37371433 Free PMC article.
6,435 results