Recent clinical advances in hereditary spinocerebellar degeneration
Author:
Affiliation:
1. Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University
Publisher
Societas Neurologica Japonica
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/64/3/64_cn-001931/_pdf
Reference55 articles.
1. 1) 「脊髄小脳変性症・多系統萎縮症診療ガイドライン」作成委員会編.脊髄小脳変性症・多系統萎縮症診療ガイドライン2018.東京:南江堂;2018.
2. 2) Tsuji S, Onodera O, Goto J, et al. Sporadic ataxias in Japan—a population-based epidemiological study. Cerebellum 2008;7:189-197.
3. 3) Sasaki H, Yabe I, Yamashita I, et al. Prevalence of triplet repeat expansion in ataxia patients from Hokkaido, the northernmost island of Japan. J Neurol Sci 2000;175:45-51.
4. 4) Basri R, Yabe I, Soma H, et al. Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families. J Hum Genet 2007;52:848-855.
5. 5) Mizushima K, Shibata Y, Shirai S, et al. Prevalence of repeat expansions causing autosomal dominant spinocerebellar ataxias in Hokkaido, the northernmost island of Japan. J Hum Genet Advance Publication, 2023; https://doi.org/10.1038/s10038-023-01200-x.
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