An approach to the patient with late-onset cerebellar ataxia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical)
Link
http://www.nature.com/articles/ncpneuro0319.pdf
Reference18 articles.
1. Maschke M et al. (2005) Clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypes. Mov Disord 20: 1405–1412
2. Kerber KA et al. (2005) Late-onset pure cerebellar ataxia: Differentiating those with and without identifiable mutations. J Neurol Sci 238: 41–45
3. Schols L et al. (2004) Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol 3: 291–304
4. van de Warrenburg BPC et al. (2005) Recent advances in hereditary spinocerebellar ataxias. J Neuropathol Exp Neurol 64: 171–180
5. Zhuchenko O et al. (1997) Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamate expansions in the α1A-voltage-dependent calcium channel. Nat Gen 15: 62–69
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