Sporadic SCA8 mutation resembling corticobasal degeneration

Parkinsonism and Related Disorders

Volumn 11, Issue 3, 2005, Pages 147-150

  Baba, Yasuhiko ^a   Uitti, Ryan J ^a   Farrer, Matthew J ^a   Wszolek, Zbigniew K ^a  

^a MAYO CLINIC   (United States)

Author keywords

Clinical presentation; Corticobasal degeneration; Spinocerebellar ataxia type 8; Sporadic

Indexed keywords

DOPAMINE RECEPTOR STIMULATING AGENT; LEVODOPA;

AGED; ARTICLE; CASE REPORT; CLINICAL FEATURE; CORTICOBASAL DEGENERATION; DISEASE COURSE; FUNCTIONAL ASSESSMENT; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; HUMAN; LABORATORY TEST; MALE; MEDICAL EXAMINATION; PHENOTYPIC VARIATION; PRIORITY JOURNAL; SPINOCEREBELLAR ATAXIA TYPE 8; SPINOCEREBELLAR DEGENERATION; TREATMENT FAILURE;

EID: 17044388145     PISSN: 13538020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.parkreldis.2004.10.008     Document Type: Article

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