메뉴 건너뛰기




Volumn 59, Issue 10, 2002, Pages 1625-1627

SCA-2 presenting as parkinsonism in an Alberta family: Clinical, genetic, and PET findings

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA SYNUCLEIN; LEVODOPA; PARKIN;

EID: 0037180520     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000035625.19871.DC     Document Type: Review
Times cited : (89)

References (10)
  • 1
    • 0030744876 scopus 로고    scopus 로고
    • Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
    • Polymeropoulos MH, Lavedan C, Leroy E, et al. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science 1997;276:2045-2047.
    • (1997) Science , vol.276 , pp. 2045-2047
    • Polymeropoulos, M.H.1    Lavedan, C.2    Leroy, E.3
  • 2
    • 0032499264 scopus 로고    scopus 로고
    • Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
    • Kitada T, Asakawa S, Hattori N, et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998;392:605-608.
    • (1998) Nature , vol.392 , pp. 605-608
    • Kitada, T.1    Asakawa, S.2    Hattori, N.3
  • 3
    • 0033677633 scopus 로고    scopus 로고
    • Linkage exclusion in French families with probable Parkinson's Disease
    • Farrer M, Destee T, Bequet E, et al. Linkage exclusion in French families with probable Parkinson's Disease. Mov Disord 2000;15:1075-1083.
    • (2000) Mov Disord , vol.15 , pp. 1075-1083
    • Farrer, M.1    Destee, T.2    Bequet, E.3
  • 4
    • 0034718577 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese
    • Gwinn-Hardy K, Chen JY, Liu H-C, 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
  • 5
    • 18844471416 scopus 로고    scopus 로고
    • In vivo positron emission tomographic evidence for compensatory changes in presynaptic dopaminergic nerve terminals in Parkinson's disease
    • Lee CS, Samii A, Sossi V, et al. In vivo positron emission tomographic evidence for compensatory changes in presynaptic dopaminergic nerve terminals in Parkinson's disease. Ann Neurol 2000;47:493-503.
    • (2000) Ann Neurol , vol.47 , pp. 493-503
    • Lee, C.S.1    Samii, A.2    Sossi, V.3
  • 6
    • 0035092779 scopus 로고    scopus 로고
    • Biochemical variations in the synaptic level of dopamine precedes motor fluctuations in Parkinson's disease: PET evidence of increased dopamine turnover
    • de la Fuente-Fernandez R, Lu. J-Q, Sossi V, et al. Biochemical variations in the synaptic level of dopamine precedes motor fluctuations in Parkinson's disease: PET evidence of increased dopamine turnover. Ann Neurol 2001;49:298-303.
    • (2001) Ann Neurol , vol.49 , pp. 298-303
    • De la Fuente-Fernandez, R.1    Lu, J.-Q.2    Sossi, V.3
  • 7
    • 0030292488 scopus 로고    scopus 로고
    • Identification of the SCA-2 gene: Moderate expansion of a normally biallelic trinucleotide repeat
    • Pulst SM, Nechiporuk A, Nechiporuk T, et al. Identification of the SCA-2 gene: Moderate expansion of a normally biallelic trinucleotide repeat. Nat Genet 1996;14:269-276.
    • (1996) Nat Genet , vol.14 , pp. 269-276
    • Pulst, S.M.1    Nechiporuk, A.2    Nechiporuk, T.3
  • 8
    • 0030698691 scopus 로고    scopus 로고
    • Olfactory dysfunction in familial parkinsonism
    • Markopoulou K, Larsen KW, Wszolek EK, et al. Olfactory dysfunction in familial parkinsonism. Neurology 1997;49: 1262-1267.
    • (1997) Neurology , vol.49 , pp. 1262-1267
    • Markopoulou, K.1    Larsen, K.W.2    Wszolek, E.K.3
  • 9
    • 0035199626 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism
    • Shan DE, Soong BW, Sun CM, et al. Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism. Ann Neurol 2001;50:812-815.
    • (2001) Ann Neurol , vol.50 , pp. 812-815
    • Shan, D.E.1    Soong, B.W.2    Sun, C.M.3
  • 10
    • 0032796303 scopus 로고    scopus 로고
    • PET studies of parkinsonism associated with mutation in the alpha-synuclein gene
    • Samii A, Markopoulou K, Wszolek ZK, et al. PET studies of parkinsonism associated with mutation in the alpha-synuclein gene. Neurology 1999;53:2097-2102.
    • (1999) Neurology , vol.53 , pp. 2097-2102
    • Samii, A.1    Markopoulou, K.2    Wszolek, Z.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.