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Volumn 35, Issue 4, 2008, Pages 488-490

Spinocerebellar ataxia type 12 was not found in Korean Parkinsonian patients

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE; CYTIDINE; PHOSPHOPROTEIN PHOSPHATASE 2A; TRINUCLEOTIDE; URIDINE;

EID: 55049083785     PISSN: 03171671     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0317167100009161     Document Type: Article
Times cited : (6)

References (20)
  • 1
    • 17844389364 scopus 로고    scopus 로고
    • The wide spectrum of spinocerebellar ataxias (SCAs)
    • Manto MU. The wide spectrum of spinocerebellar ataxias (SCAs). Cerebellum. 2005;4:2-6.
    • (2005) Cerebellum , vol.4 , pp. 2-6
    • Manto, M.U.1
  • 3
    • 0035118860 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family
    • Gwinn-Hardy K, Singleton A, O'Suilleabhain P, Boss M, Nicholl D, Adam A, et al. Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family. Arch Neurol. 2001;58:296-9.
    • (2001) Arch Neurol , vol.58 , pp. 296-299
    • Gwinn-Hardy, K.1    Singleton, A.2    O'Suilleabhain, P.3    Boss, M.4    Nicholl, D.5    Adam, A.6
  • 7
    • 8844259530 scopus 로고    scopus 로고
    • Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: Clinical implications
    • Shan DE, Liu RS, Sun CM, Lee SJ, Liao KK, Soong BW. Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: clinical implications. Mov Disord. 2004;19:1357-60.
    • (2004) Mov Disord , vol.19 , pp. 1357-1360
    • Shan, D.E.1    Liu, R.S.2    Sun, C.M.3    Lee, S.J.4    Liao, K.K.5    Soong, B.W.6
  • 8
    • 4544319896 scopus 로고    scopus 로고
    • SCA2 presenting as levodopa-responsive parkinsonism in a young patient from the United Kingdom: A case report
    • Wilkins A, Brown JM, Barker RA. SCA2 presenting as levodopa-responsive parkinsonism in a young patient from the United Kingdom: a case report. Mov Disord. 2004;19:593-5.
    • (2004) Mov Disord , vol.19 , pp. 593-595
    • Wilkins, A.1    Brown, J.M.2    Barker, R.A.3
  • 9
    • 10744231577 scopus 로고    scopus 로고
    • Genetic testing in spinocerebellar ataxia in Taiwan: Expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease
    • Wu YR, Lin HY, Chen CM, Gwinn-Hardy K, Ro LS, Wang YC, et al. Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease. Clin Genet. 2004: 65: 209-214.
    • (2004) Clin Genet , vol.65 , pp. 209-214
    • Wu, Y.R.1    Lin, H.Y.2    Chen, C.M.3    Gwinn-Hardy, K.4    Ro, L.S.5    Wang, Y.C.6
  • 10
    • 21144433087 scopus 로고    scopus 로고
    • Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease
    • Simon-Sanchez J, Hanson M, Singleton A, Hernandez D, McInerney A, Nussbaum R, et al. Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease. Neurosci Lett. 2005;382:191-4.
    • (2005) Neurosci Lett , vol.382 , pp. 191-194
    • Simon-Sanchez, J.1    Hanson, M.2    Singleton, A.3    Hernandez, D.4    McInerney, A.5    Nussbaum, R.6
  • 11
    • 33745512490 scopus 로고    scopus 로고
    • Genetic analysis of SCA2, 3 and 17 in idiopathic Parkinson's disease
    • Lim SW, Zhao Y, Chua E, Law HY, Yuen Y, Pavanni R, et al. Genetic analysis of SCA2, 3 and 17 in idiopathic Parkinson's disease. Neurosci Lett. 2006;403:11-14.
    • (2006) Neurosci Lett , vol.403 , pp. 11-14
    • Lim, S.W.1    Zhao, Y.2    Chua, E.3    Law, H.Y.4    Yuen, Y.5    Pavanni, R.6
  • 13
    • 35348914402 scopus 로고    scopus 로고
    • Importance of low-range CAG expansion and CAA interruption in SCA2 Parkinsonism
    • Kim JM, Hong S, Kim GP, Choi YJ, Kim YK, Park SS, et al. Importance of low-range CAG expansion and CAA interruption in SCA2 Parkinsonism. Arch Neurol. 2007;64:1510-8.
    • (2007) Arch Neurol , vol.64 , pp. 1510-1518
    • Kim, J.M.1    Hong, S.2    Kim, G.P.3    Choi, Y.J.4    Kim, Y.K.5    Park, S.S.6
  • 16
    • 0035115573 scopus 로고    scopus 로고
    • SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study of an Indian family
    • Fujigasaki H, Verma IC, Camuzat A, Margolis RL, Zander C, Lebre AS, et al. SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family. Ann Neurol. 2001;49:117-21.
    • (2001) Ann Neurol , vol.49 , pp. 117-121
    • Fujigasaki, H.1    Verma, I.C.2    Camuzat, A.3    Margolis, R.L.4    Zander, C.5    Lebre, A.S.6
  • 18
    • 0026514953 scopus 로고
    • Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinicopathological study of 100 cases
    • Hughes AJ, Daniel SE, Kilford L, Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinicopathological study of 100 cases. J Neurol Neurosurg Psychiatry. 1992;55:181-4.
    • (1992) J Neurol Neurosurg Psychiatry , vol.55 , pp. 181-184
    • Hughes, A.J.1    Daniel, S.E.2    Kilford, L.3    Lees, A.J.4
  • 20
    • 20244380183 scopus 로고    scopus 로고
    • Analysis of polyglutamine-coding repeats in the TATA-binding protein in different neurodegenerative diseases
    • Wu YR, Fung HC, Lee-Chen GJ, Gwinn-Hardy K, Ro LS, Chen ST, et al. Analysis of polyglutamine-coding repeats in the TATA-binding protein in different neurodegenerative diseases. J Neural Transm. 2005;112:539-46.
    • (2005) J Neural Transm , vol.112 , pp. 539-546
    • Wu, Y.R.1    Fung, H.C.2    Lee-Chen, G.J.3    Gwinn-Hardy, K.4    Ro, L.S.5    Chen, S.T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.