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Phenotypic and molecular diversities of spinocerebellar ataxia type 2 in Japan.
Inada R, Hirano M, Oka N, Samukawa M, Saigoh K, Suzuki H, Udaka F, Hashiguchi A, Takashima H, Hamada Y, Nakamura Y, Kusunoki S. Inada R, et al. Among authors: nakamura y. J Neurol. 2021 Aug;268(8):2933-2942. doi: 10.1007/s00415-021-10467-z. Epub 2021 Feb 24. J Neurol. 2021. PMID: 33625581
PSP-Phenotype in SCA8: Case Report and Systemic Review.
Samukawa M, Hirano M, Saigoh K, Kawai S, Hamada Y, Takahashi D, Nakamura Y, Kusunoki S. Samukawa M, et al. Among authors: nakamura y. Cerebellum. 2019 Feb;18(1):76-84. doi: 10.1007/s12311-018-0955-0. Cerebellum. 2019. PMID: 29916049
Multiple system involvement in a Japanese patient with a V31A mutation in the SOD1 gene.
Sakamoto H, Akamatsu M, Hirano M, Saigoh K, Ueno S, Isono C, Kusunoki S, Nakamura Y. Sakamoto H, et al. Among authors: nakamura y. Amyotroph Lateral Scler Frontotemporal Degener. 2014 Jun;15(3-4):312-4. doi: 10.3109/21678421.2013.873051. Epub 2014 Mar 10. Amyotroph Lateral Scler Frontotemporal Degener. 2014. PMID: 24611504
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