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Genetic Variations and Neuropathologic Features of Patients with PRKN Mutations.
Seike N, Yokoseki A, Takeuchi R, Saito K, Miyahara H, Miyashita A, Ikeda T, Aida I, Nakajima T, Kanazawa M, Wakabayashi M, Toyoshima Y, Takahashi H, Matsumoto R, Toda T, Onodera O, Ishikawa A, Ikeuchi T, Kakita A. Seike N, et al. Among authors: nakajima t. Mov Disord. 2021 Jul;36(7):1634-1643. doi: 10.1002/mds.28521. Epub 2021 Feb 11. Mov Disord. 2021. PMID: 33570211
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: nakajima t. 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.
Efficacy and tolerance of gastrostomy feeding in Japanese muscular dystrophy patients.
Mizuno T, Komaki H, Sasaki M, Takanoha S, Kuroda K, Kon K, Mamiya S, Yoshioka M, Yatabe K, Mikata T, Ishihara T, Nakajima T, Watanabe H, Konagaya M, Mitani M, Konishi T, Tokita Y, Fukuda K, Tatara K, Maruta K, Imamura S, Shimazaki R, Ishikawa K, Saito T, Shinno S. Mizuno T, et al. Among authors: nakajima t. Brain Dev. 2012 Oct;34(9):756-62. doi: 10.1016/j.braindev.2011.11.012. Epub 2011 Dec 26. Brain Dev. 2012. PMID: 22204944
5,997 results