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Journal Abstract Search

311 related items for PubMed ID: 22520093

  • 1. 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]

  • 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 15; 57(4):540-4. PubMed ID: 10768629
    [Abstract] [Full Text] [Related]

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

  • 4. 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]

  • 5. 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]

  • 6. The wide spectrum of spinocerebellar ataxias (SCAs).
    Manto MU.
    Cerebellum; 2005 May 15; 4(1):2-6. PubMed ID: 15895552
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. The hereditary spinocerebellar ataxias in Japan.
    Sasaki H, Yabe I, Tashiro K.
    Cytogenet Genome Res; 2003 Dec 31; 100(1-4):198-205. PubMed ID: 14526181
    [Abstract] [Full Text] [Related]

  • 9. 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 31; 36(6):482-9. PubMed ID: 21743138
    [Abstract] [Full Text] [Related]

  • 10. [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 31; 22(1):1-4. PubMed ID: 15696468
    [Abstract] [Full Text] [Related]

  • 11. [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
    [Abstract] [Full Text] [Related]

  • 12.
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  • 13. 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]

  • 14. Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia.
    Storey E, du Sart D, Shaw JH, Lorentzos P, Kelly L, McKinley Gardner RJ, Forrest SM, Biros I, Nicholson GA.
    Am J Med Genet; 2000 Dec 11; 95(4):351-7. PubMed ID: 11186889
    [Abstract] [Full Text] [Related]

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

  • 16. 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]

  • 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. Mutational screening of 320 Brazilian patients with autosomal dominant spinocerebellar ataxia.
    Cintra VP, Lourenço CM, Marques SE, de Oliveira LM, Tumas V, Marques W.
    J Neurol Sci; 2014 Dec 15; 347(1-2):375-9. PubMed ID: 25466696
    [Abstract] [Full Text] [Related]

  • 19. Friedreich's ataxia and other hereditary ataxias in Greece: an 18-year perspective.
    Koutsis G, Kladi A, Karadima G, Houlden H, Wood NW, Christodoulou K, Panas M.
    J Neurol Sci; 2014 Jan 15; 336(1-2):87-92. PubMed ID: 24209901
    [Abstract] [Full Text] [Related]

  • 20. Frequency analysis and clinical characterization of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Korean patients.
    Lee WY, Jin DK, Oh MR, Lee JE, Song SM, Lee EA, Kim GM, Chung JS, Lee KH.
    Arch Neurol; 2003 Jun 15; 60(6):858-63. PubMed ID: 12810491
    [Abstract] [Full Text] [Related]

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