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Volumn 13, Issue 2, 2012, Pages 133-140

JPH3 repeat expansions cause a progressive akinetic-rigid syndrome with severe dementia and putaminal rim in a five-generation African-American family

Author keywords

African American; Chorea; Dementia; Huntington's disease; JPH3; Parkinsonism; Putaminal rim

Indexed keywords

JUNCTOPHILLIN 3; LEVODOPA; PROTEIN; UNCLASSIFIED DRUG;

EID: 84862672230     PISSN: 13646745     EISSN: 13646753     Source Type: Journal    
DOI: 10.1007/s10048-012-0318-9     Document Type: Article
Times cited : (25)

References (21)
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    • Nonchoreic movement disorders as initial manifestations of Huntington's disease
    • Becker N, Munhoz RP, Raskin S, Cesar W, Teive HA (2007) Nonchoreic movement disorders as initial manifestations of Huntington's disease. Arq Neuro-Psiquiatr 65:402-405
    • (2007) Arq Neuro-Psiquiatr , vol.65 , pp. 402-405
    • Becker, N.1    Munhoz, R.P.2    Raskin, S.3    Cesar, W.4    Teive, H.A.5
  • 10
    • 30444440181 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 17: Extension of phenotype with putaminal rim hyperintensity on magnetic resonance imaging
    • Loy CT, Sweeney MG, Davis MB, Wills AJ, Sawle GV, Lees AJ, Tabrizi SJ (2005) Spinocerebellar ataxia type 17: extension of phenotype with putaminal rim hyperintensity on magnetic resonance imaging. Mov Disord 20:1521-1523
    • (2005) Mov Disord , vol.20 , pp. 1521-1523
    • Loy, C.T.1    Sweeney, M.G.2    Davis, M.B.3    Wills, A.J.4    Sawle, G.V.5    Lees, A.J.6    Tabrizi, S.J.7
  • 18
    • 36048934793 scopus 로고    scopus 로고
    • HDL2 mutations are an important cause of Huntington's disease in patients with African ancestry
    • Krause A, Hetem C, Holmes SE, Margolis RL (2005) HDL2 mutations are an important cause of Huntington's disease in patients with African ancestry. J Neurol Neurosurg Psychiatry 76:A16-A26
    • (2005) J Neurol Neurosurg Psychiatry , vol.76
    • Krause, A.1    Hetem, C.2    Holmes, S.E.3    Margolis, R.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.