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Historical and More Common Nongenetic Movement Disorders From Asia
Download from doi.orgNine Hereditary Movement Disorders First Described in Asia: Their History and Evolution
Download from doi.orgEye‐of‐Tiger Sign in Globus Pallidus: A Novel Radiological Feature of Spinocerebellar Ataxia Type 28
Download from onlinelibrary.wiley.comMitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy
Download from academic.oup.comNovel Phenotype of 6p25 Deletion Syndrome Presenting Juvenile Parkinsonism and Brain Calcification
Download from api.wiley.comHeterogeneous nonataxic phenotypes of spinocerebellar ataxia in a Taiwanese population
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