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Volumn 76, Issue 24, 2011, Pages 2050-2051

Amyotrophic lateral sclerosis and spinocerebellar ataxia 2

Author keywords

[No Author keywords available]

Indexed keywords

NUCLEIC ACID BINDING PROTEIN; POLYGLUTAMINE; PROTEIN SPINOCEREBELLAR ATAXIA 2; UNCLASSIFIED DRUG;

EID: 79959636879     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e31821f4498     Document Type: Editorial
Times cited : (11)

References (15)
  • 4
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    • Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
    • Kwiatkowski TJ Jr, Bosco DA, Leclerc AL, et al. Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 2009;323: 1205-1208.
    • (2009) Science , vol.323 , pp. 1205-1208
    • Kwiatkowski Jr., T.J.1    Bosco, D.A.2    Leclerc, A.L.3
  • 5
    • 78649941297 scopus 로고    scopus 로고
    • Exome sequencing reveals VCP mutations as a cause of familial ALS
    • Johnson JO, Mandrioli J, Benatar M, et al. Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron 2010;68:857-864.
    • (2010) Neuron , vol.68 , pp. 857-864
    • Johnson, J.O.1    Mandrioli, J.2    Benatar, M.3
  • 8
    • 77956155218 scopus 로고    scopus 로고
    • Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS
    • Elden AC, Kim HJ, Hart MP, et al. Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS. Nature 2010;466:1069-1075.
    • (2010) Nature , vol.466 , pp. 1069-1075
    • Elden, A.C.1    Kim, H.J.2    Hart, M.P.3
  • 9
    • 79959653680 scopus 로고    scopus 로고
    • Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2
    • Van Damme P, Veldink JH, van Blitterswijk M, et al. Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2. Neurology 2011; 76:2066-2072.
    • (2011) Neurology , vol.76 , pp. 2066-2072
    • Van Damme, P.1    Veldink, J.H.2    Van Blitterswijk, M.3
  • 10
    • 73449090497 scopus 로고    scopus 로고
    • Rare association of motor neuron disease and spinocerebellar ataxia type 2 (SCA2): A new case and review of the literature
    • Nanetti L, Fancellu R, Tomasello C, et al. Rare association of motor neuron disease and spinocerebellar ataxia type 2 (SCA2): a new case and review of the literature. J Neurol 2009;256:1926-1928.
    • (2009) J Neurol , vol.256 , pp. 1926-1928
    • Nanetti, L.1    Fancellu, R.2    Tomasello, C.3
  • 11
    • 0034718577 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese
    • Gwinn-Hardy K, Chen JY, Liu HC, et al. Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese. Neurology 2000;55:800-805.
    • (2000) Neurology , vol.55 , pp. 800-805
    • Gwinn-Hardy, K.1    Chen, J.Y.2    Liu, H.C.3
  • 13
    • 70349592269 scopus 로고    scopus 로고
    • Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
    • van Es MA, Veldink JH, Saris CG, et al. Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nat Genet 2009;41:1083-1087.
    • (2009) Nat Genet , vol.41 , pp. 1083-1087
    • Van Es, M.A.1    Veldink, J.H.2    Saris, C.G.3
  • 14
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    • Evaluating the prevalence of polyglutamine repeat expansions in amyotrophic lateral sclerosis
    • Lee T, Li YR, Chesi A, et al. Evaluating the prevalence of polyglutamine repeat expansions in amyotrophic lateral sclerosis. Neurology 2011;76:2062-2065.
    • (2011) Neurology , vol.76 , pp. 2062-2065
    • Lee, T.1    Li, Y.R.2    Chesi, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.