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404 related items for PubMed ID: 17062934

  • 21. [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; 16(5):281-4. PubMed ID: 10514531
    [Abstract] [Full Text] [Related]

  • 22. 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; 111(3):154-62. PubMed ID: 15691283
    [Abstract] [Full Text] [Related]

  • 23. 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
    [Abstract] [Full Text] [Related]

  • 24. SCA 1, SCA 2 & SCA 3/MJD mutations in ataxia syndromes in southern India.
    Krishna N, Mohan S, Yashavantha BS, Rammurthy A, Kiran Kumar HB, Mittal U, Tyagi S, Mukerji M, Jain S, Pal PK, Purushottam M.
    Indian J Med Res; 2007 Nov 28; 126(5):465-70. PubMed ID: 18160752
    [Abstract] [Full Text] [Related]

  • 25. Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.
    Globas C, du Montcel ST, Baliko L, Boesch S, Depondt C, DiDonato S, Durr A, Filla A, Klockgether T, Mariotti C, Melegh B, Rakowicz M, Ribai P, Rola R, Schmitz-Hubsch T, Szymanski S, Timmann D, Van de Warrenburg BP, Bauer P, Schols L.
    Mov Disord; 2008 Nov 15; 23(15):2232-8. PubMed ID: 18759344
    [Abstract] [Full Text] [Related]

  • 26. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia.
    Geschwind DH, Perlman S, Figueroa CP, Treiman LJ, Pulst SM.
    Am J Hum Genet; 1997 Apr 15; 60(4):842-50. PubMed ID: 9106530
    [Abstract] [Full Text] [Related]

  • 27. Spinocerebellar ataxia types 2 and 3 segregating simultaneously in a single family.
    França MC, Calcagnotto ME, da Costa JC, Lopes-Cendes I.
    Mov Disord; 2006 Jul 15; 21(7):1051-3. PubMed ID: 16628604
    [Abstract] [Full Text] [Related]

  • 28. Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.
    Jacobi H, du Montcel ST, Bauer P, Giunti P, Cook A, Labrum R, Parkinson MH, Durr A, Brice A, Charles P, Marelli C, Mariotti C, Nanetti L, Panzeri M, Rakowicz M, Sulek A, Sobanska A, Schmitz-Hübsch T, Schöls L, Hengel H, Baliko L, Melegh B, Filla A, Antenora A, Infante J, Berciano J, van de Warrenburg BP, Timmann D, Szymanski S, Boesch S, Kang JS, Pandolfo M, Schulz JB, Molho S, Diallo A, Klockgether T.
    Lancet Neurol; 2015 Nov 15; 14(11):1101-8. PubMed ID: 26377379
    [Abstract] [Full Text] [Related]

  • 29. Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes.
    de Castilhos RM, Furtado GV, Gheno TC, Schaeffer P, Russo A, Barsottini O, Pedroso JL, Salarini DZ, Vargas FR, de Lima MA, Godeiro C, Santana-da-Silva LC, Toralles MB, Santos S, van der Linden H, Wanderley HY, de Medeiros PF, Pereira ET, Ribeiro E, Saraiva-Pereira ML, Jardim LB, Rede Neurogenetica.
    Cerebellum; 2014 Feb 15; 13(1):17-28. PubMed ID: 23943520
    [Abstract] [Full Text] [Related]

  • 30. Cell biology of spinocerebellar ataxia.
    Orr HT.
    J Cell Biol; 2012 Apr 16; 197(2):167-77. PubMed ID: 22508507
    [Abstract] [Full Text] [Related]

  • 31. 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]

  • 32. The hereditary adult-onset ataxias in South Africa.
    Bryer A, Krause A, Bill P, Davids V, Bryant D, Butler J, Heckmann J, Ramesar R, Greenberg J.
    J Neurol Sci; 2003 Dec 15; 216(1):47-54. PubMed ID: 14607302
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  • 33. 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]

  • 34. [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]

  • 35. Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.
    Leggo J, Dalton A, Morrison PJ, Dodge A, Connarty M, Kotze MJ, Rubinsztein DC.
    J Med Genet; 1997 Dec 15; 34(12):982-5. PubMed ID: 9429138
    [Abstract] [Full Text] [Related]

  • 36. Should spinocerebellar ataxias be included in the differential diagnosis for Huntington's diseases-like syndromes?
    Pedroso JL, de Freitas ME, Albuquerque MV, Saraiva-Pereira ML, Jardim LB, Barsottini OG.
    J Neurol Sci; 2014 Dec 15; 347(1-2):356-8. PubMed ID: 25456461
    [Abstract] [Full Text] [Related]

  • 37. Genetic testing for spinocerebellar ataxias in patients diagnosed as Parkinson's disease in Bangladesh.
    Rahman MS, Sarkar MA, Rahman MF, Paul SK, Nagai SY, Uddin MJ, Toda T.
    Mymensingh Med J; 2015 Jan 15; 24(1):44-51. PubMed ID: 25725667
    [Abstract] [Full Text] [Related]

  • 38. 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
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  • 39. Genetic analysis of SCA 2 and 3 repeat expansions in essential tremor and atypical Parkinsonism.
    Tan EK, Tong J, Pavanni R, Wong MC, Zhao Y.
    Mov Disord; 2007 Oct 15; 22(13):1971-4. PubMed ID: 17712857
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  • 40. 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]

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