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225 related items for PubMed ID: 15696468

  • 1. [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; 22(1):1-4. PubMed ID: 15696468
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Frequency analysis of autosomal dominant cerebellar ataxias in Taiwanese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
    Soong B W, Lu Y C, Choo K B, Lee H Y.
    Arch Neurol; 2001 Jul 15; 58(7):1105-9. PubMed ID: 11448300
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 57(4):540-4. PubMed ID: 10768629
    [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 15; 36(6):482-9. PubMed ID: 21743138
    [Abstract] [Full Text] [Related]

  • 7. 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 15; 61(5):727-33. PubMed ID: 15148151
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 109(5):355-60. PubMed ID: 15080863
    [Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. [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]

  • 11. [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 15; 31(5):702-5. PubMed ID: 17062934
    [Abstract] [Full Text] [Related]

  • 12. [Polynucleotide repeat expansion of nine spinocerebellar ataxia subtypes and dentatorubral-pallidoluysian atrophy in healthy Chinese Han population].
    Wang JL, Wu YQ, Lei LF, Shen L, Jiang H, Zhou YF, Yi JP, Zhou J, Yan XX, Pan Q, Xia K, Tang BS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Oct 15; 27(5):501-5. PubMed ID: 20931525
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre study.
    Choubtum L, Witoonpanich P, Hanchaiphiboolkul S, Bhidayasiri R, Jitkritsadakul O, Pongpakdee S, Wetchaphanphesat S, Boonkongchuen P, Pulkes T.
    BMC Neurol; 2015 Sep 15; 15():166. PubMed ID: 26374734
    [Abstract] [Full Text] [Related]

  • 15. 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 15; 106(6):597-604. PubMed ID: 10942107
    [Abstract] [Full Text] [Related]

  • 16. Frequency of spinocerebellar ataxia mutations in the Kinki district of Japan.
    Matsumura R, Futamura N, Ando N, Ueno S.
    Acta Neurol Scand; 2003 Jan 15; 107(1):38-41. PubMed ID: 12542511
    [Abstract] [Full Text] [Related]

  • 17. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
    Tang B, Xia J, Wang D, Tang X, Shen L, Liu C, Dai H, Yan X, Pan Q, Xiao J, Zhang B, Ou Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct 15; 16(5):281-4. PubMed ID: 10514531
    [Abstract] [Full Text] [Related]

  • 18. Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxia.
    Koutsis G, Pemble S, Sweeney MG, Paudel R, Wood NW, Panas M, Kladi A, Houlden H.
    J Neurol Sci; 2012 Jul 15; 318(1-2):178-80. PubMed ID: 22520093
    [Abstract] [Full Text] [Related]

  • 19. [Studies on the CTA/CTG trinucleotide repeats of ATXN8OS gene in Chinese Hans].
    Wang J, Zhang S, Xu Q, Li X, Song X, Jiang H, Shen L, Yan X, Pan Q, Xia K, Tang B.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct 15; 25(5):511-4. PubMed ID: 18841561
    [Abstract] [Full Text] [Related]

  • 20. [Gene diagnosis and CAG repeat analysis of spinocerebellar ataxia cases of Guangxi region].
    Tan JQ, Wang P, Hu QP, Li SF, Shu W, Ma J, Fang L, Hua R, Ding Y, Yuan ZG.
    Yi Chuan; 2009 Jun 15; 31(6):605-10. PubMed ID: 19586860
    [Abstract] [Full Text] [Related]

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