Treatment and management issues in ataxic diseases
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Publisher
Elsevier
Reference240 articles.
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1. The inherited ataxias;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020
2. A simple saccadic reading test to assess ocular motor function in cerebellar ataxia;PLOS ONE;2018-11-07
3. A homozygous mutation ofVWA3Bcauses cerebellar ataxia with intellectual disability;Journal of Neurology, Neurosurgery & Psychiatry;2015-07-08
4. Molecular mechanism of Spinocerebellar Ataxia type 6: glutamine repeat disorder, channelopathy and transcriptional dysregulation. The multifaceted aspects of a single mutation;Frontiers in Cellular Neuroscience;2015-02-16
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