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Journal Abstract Search

466 related items for PubMed ID: 12116198

  • 1. Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients.
    Maruyama H, Izumi Y, Morino H, Oda M, Toji H, Nakamura S, Kawakami H.
    Am J Med Genet; 2002 Jul 08; 114(5):578-83. PubMed ID: 12116198
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  • 3. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
    Brusco A, Gellera C, Cagnoli C, Saluto A, Castucci A, Michielotto C, Fetoni V, Mariotti C, Migone N, Di Donato S, Taroni F.
    Arch Neurol; 2004 May 08; 61(5):727-33. PubMed ID: 15148151
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  • 6. [Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China].
    Song XW, Tang BS, Jiang H, Shen L, Yang Q, Liao SS, Li QH, Tang JG.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2006 Oct 08; 31(5):702-5. PubMed ID: 17062934
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  • 8. [SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].
    Tang B, Wang D, Xia J.
    Zhonghua Yi Xue Za Zhi; 1997 Nov 08; 77(11):819-22. PubMed ID: 9772474
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  • 9. Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families.
    Silveira I, Coutinho P, Maciel P, Gaspar C, Hayes S, Dias A, Guimarães J, Loureiro L, Sequeiros J, Rouleau GA.
    Am J Med Genet; 1998 Mar 28; 81(2):134-8. PubMed ID: 9613852
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  • 13. Molecular analysis of Spinocerebellar ataxias in Koreans: frequencies and reference ranges of SCA1, SCA2, SCA3, SCA6, and SCA7.
    Kim JY, Park SS, Joo SI, Kim JM, Jeon BS.
    Mol Cells; 2001 Dec 31; 12(3):336-41. PubMed ID: 11804332
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  • 14. A genetic epidemiological study of spinocerebellar ataxias in Tottori prefecture, Japan.
    Mori M, Adachi Y, Kusumi M, Nakashima K.
    Neuroepidemiology; 2001 May 31; 20(2):144-9. PubMed ID: 11359084
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  • 17. [The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7].
    Yin XZ, Zhang BR, Wu DW, Tian J, Zhang H.
    Yi Chuan; 2007 Jun 31; 29(6):688-92. PubMed ID: 17650485
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  • 18. [Studies on the CAG repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese Han].
    Wang J, Xu Q, Lei L, Shen L, Jiang H, Li X, Zhou Y, Yi J, Zhou J, Yan X, Pan Q, Xia K, Tang B.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec 31; 26(6):620-5. PubMed ID: 19953482
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  • 19. The occurrence of dominant spinocerebellar ataxias among 251 Finnish ataxia patients and the role of predisposing large normal alleles in a genetically isolated population.
    Juvonen V, Hietala M, Kairisto V, Savontaus ML.
    Acta Neurol Scand; 2005 Mar 31; 111(3):154-62. PubMed ID: 15691283
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  • 20. Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
    Jiang H, Tang BS, Xu B, Zhao GH, Shen L, Tang JG, Li QH, Xia K.
    Chin Med J (Engl); 2005 May 20; 118(10):837-43. PubMed ID: 15989765
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