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Volumn 73, Issue 20, 2009, Pages 1708-1709

Extrapyramidal signs are a common feature of spinocerebellar ataxia type 17

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; PROTEIN SPINOCEREBELLAR ATAXIA 17; TATA BINDING PROTEIN; UNCLASSIFIED DRUG;

EID: 73449105744     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3181c1df0c     Document Type: Article
Times cited : (9)

References (7)
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    • A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: A new polyglutamine disease?
    • Koide R, Kobayashi S, Shimohata T, et al. A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease? Hum Mol Genet 1999;8:2047-2053.
    • (1999) Hum Mol Genet , vol.8 , pp. 2047-2053
    • Koide, R.1    Kobayashi, S.2    Shimohata, T.3
  • 2
    • 0042837890 scopus 로고    scopus 로고
    • Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17)
    • Rolfs A, Koeppen AH, Bauer I, et al. Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17). Ann Neurol 2003;54:367-375.
    • (2003) Ann Neurol , vol.54 , pp. 367-375
    • Rolfs, A.1    Koeppen, A.H.2    Bauer, I.3
  • 3
    • 15244339141 scopus 로고    scopus 로고
    • Regional features of autosomal-dominant cerebellar ataxia in Nagano: Clinical and molecular genetic analysis of 86 families
    • Shimizu Y, Yoshida K, Okano T, et al. Regional features of autosomal-dominant cerebellar ataxia in Nagano: clinical and molecular genetic analysis of 86 families. J Hum Genet 2004;49:610-616.
    • (2004) J Hum Genet , vol.49 , pp. 610-616
    • Shimizu, Y.1    Yoshida, K.2    Okano, T.3
  • 4
    • 67449136057 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 17 mutation as a causative and susceptibility gene in parkinsonism
    • Kim JY, Kim SY, Kim JM, et al. Spinocerebellar ataxia type 17 mutation as a causative and susceptibility gene in parkinsonism. Neurology 2009;72:1385-1389.
    • (2009) Neurology , vol.72 , pp. 1385-1389
    • Kim, J.Y.1    Kim, S.Y.2    Kim, J.M.3
  • 5
    • 34347231996 scopus 로고    scopus 로고
    • Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population
    • Alonso E, Martinez-Ruano L, De Biase I, et al. Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population. Mov Disord 2007;22:1050-1053.
    • (2007) Mov Disord , vol.22 , pp. 1050-1053
    • Alonso, E.1    Martinez-Ruano, L.2    De Biase, I.3
  • 6
    • 44449161332 scopus 로고    scopus 로고
    • Hunting-ton's disease phenocopies are clinically and genetically heterogeneous
    • Wild EJ, Mudanohwo EE, Sweeney MG, et al. Hunting-ton's disease phenocopies are clinically and genetically heterogeneous. Mov Disord 2008;23:716-720.
    • (2008) Mov Disord , vol.23 , pp. 716-720
    • Wild, E.J.1    Mudanohwo, E.E.2    Sweeney, M.G.3
  • 7
    • 48449096757 scopus 로고    scopus 로고
    • Searching for mutation in the JPH3, ATN1 and TBP genes in Polish patients suspected of Huntington's disease and without mutation in the IT15 gene
    • Sulek-Piatkowska A, Krysa W, Zdzienicka E, et al. Searching for mutation in the JPH3, ATN1 and TBP genes in Polish patients suspected of Huntington's disease and without mutation in the IT15 gene Neurol Neurochir Pol 2008;42:203-209.
    • (2008) Neurol Neurochir Pol , vol.42 , pp. 203-209
    • Sulek-Piatkowska, A.1    Krysa, W.2    Zdzienicka, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.