Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Reference35 articles.
1. Schols L, Bauer P, Schmidt T, Schulte T, Riess O. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol. 2004;3:291–4.
2. Bird T. Hereditary ataxia overview. Ncbi.nlm.nih.gov. 2018. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1138/
3. Teive HAG, Ashizawa T. Primary and secondary ataxias. Curr Opin Neurol. 2015;28:413–22.
4. Moro A, Munhoz RP, Moscovich M, Arruda WO, Raskin S, Silveira-Moriyama L, et al. Nonmotor symptoms in patients with spinocerebellar ataxia type 10. Cerebellum. 2017;6:1–7.
5. Ashizawa T. Spinocerebellar ataxia type 10. Handb Clin Neurol. 2012;103:507–19.
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