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Journal Abstract Search

404 related items for PubMed ID: 17062934

  • 1. [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; 31(5):702-5. PubMed ID: 17062934
    [Abstract] [Full Text] [Related]

  • 2. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
    Tang B, Liu C, Shen L, Dai H, Pan Q, Jing L, Ouyang S, Xia J.
    Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629
    [Abstract] [Full Text] [Related]

  • 3. Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan.
    Tsai HF, Liu CS, Leu TM, Wen FC, Lin SJ, Liu CC, Yang DK, Li C, Hsieh M.
    Acta Neurol Scand; 2004 May; 109(5):355-60. PubMed ID: 15080863
    [Abstract] [Full Text] [Related]

  • 4. 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; 61(5):727-33. PubMed ID: 15148151
    [Abstract] [Full Text] [Related]

  • 5. Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India.
    Basu P, Chattopadhyay B, Gangopadhaya PK, Mukherjee SC, Sinha KK, Das SK, Roychoudhury S, Majumder PP, Bhattacharyya NP.
    Hum Genet; 2000 Jun; 106(6):597-604. PubMed ID: 10942107
    [Abstract] [Full Text] [Related]

  • 6. Spinocerebellar ataxias in mainland China: an updated genetic analysis among a large cohort of familial and sporadic cases.
    Wang J, Shen L, Lei L, Xu Q, Zhou J, Liu Y, Guan W, Pan Q, Xia K, Tang B, Jiang H.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2011 Jun; 36(6):482-9. PubMed ID: 21743138
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. [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 08; 29(6):688-92. PubMed ID: 17650485
    [Abstract] [Full Text] [Related]

  • 9. [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
    [Abstract] [Full Text] [Related]

  • 10. The occurrence of spinocerebellar ataxias caused by dynamic mutations in Polish patients.
    Sułek-Piatkowska A, Zdzienicka E, Raczyńska-Rakowicz M, Krysa W, Rajkiewicz M, Szirkowiec W, Zaremba J.
    Neurol Neurochir Pol; 2010 Nov 08; 44(3):238-45. PubMed ID: 20625959
    [Abstract] [Full Text] [Related]

  • 11. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.
    Pujana MA, Corral J, Gratacòs M, Combarros O, Berciano J, Genís D, Banchs I, Estivill X, Volpini V.
    Hum Genet; 1999 Jun 08; 104(6):516-22. PubMed ID: 10453742
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families.
    Jiang H, Tang B, Xia K, Zhou Y, Xu B, Zhao G, Li H, Shen L, Pan Q, Cai F.
    J Neurol Sci; 2005 Sep 15; 236(1-2):25-9. PubMed ID: 15979648
    [Abstract] [Full Text] [Related]

  • 14. A genetic epidemiological study of spinocerebellar ataxias in Tottori prefecture, Japan.
    Mori M, Adachi Y, Kusumi M, Nakashima K.
    Neuroepidemiology; 2001 May 15; 20(2):144-9. PubMed ID: 11359084
    [Abstract] [Full Text] [Related]

  • 15.
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  • 16. [Frequency analysis of autosomal dominant spinocerebellar ataxias in Han population in the Chinese mainland and clinical and molecular characterization of spinocerebellar ataxia type 6].
    Jiang H, Tang B, Xu B, Zhao GH, Shen L, Tang JG, Li QH, Xia K.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb 15; 22(1):1-4. PubMed ID: 15696468
    [Abstract] [Full Text] [Related]

  • 17. Spinocerebellar ataxias types 1, 2 and 3: age adjusted clinical severity of disease at presentation correlates with size of CAG repeat lengths.
    Netravathi M, Pal PK, Purushottam M, Thennarasu K, Mukherjee M, Jain S.
    J Neurol Sci; 2009 Feb 15; 277(1-2):83-6. PubMed ID: 19049837
    [Abstract] [Full Text] [Related]

  • 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 15; 26(6):620-5. PubMed ID: 19953482
    [Abstract] [Full Text] [Related]

  • 19. [Molecular genetics and its clinical application in the diagnosis of spinocerebellar ataxias].
    Xie QY, Liang XL, Li XH.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb 15; 22(1):71-3. PubMed ID: 15696485
    [Abstract] [Full Text] [Related]

  • 20. Diagnosis of five spinocerebellar ataxia disorders by multiplex amplification and capillary electrophoresis.
    Dorschner MO, Barden D, Stephens K.
    J Mol Diagn; 2002 May 15; 4(2):108-13. PubMed ID: 11986402
    [Abstract] [Full Text] [Related]

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