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Journal Abstract Search

755 related items for PubMed ID: 15895552

  • 21. [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; 27(5):501-5. PubMed ID: 20931525
    [Abstract] [Full Text] [Related]

  • 22. Central auditory processing in patients with spinocerebellar ataxia.
    Zeigelboim BS, de Carvalho HA, Teive HA, Liberalesso PB, Jurkiewicz AL, da Silva Abdulmassih EM, Marques JM, Cordeiro ML.
    Hear Res; 2015 Sep; 327():235-44. PubMed ID: 26183435
    [Abstract] [Full Text] [Related]

  • 23. [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; 77(11):819-22. PubMed ID: 9772474
    [Abstract] [Full Text] [Related]

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  • 25. Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease.
    Wu YR, Lin HY, Chen CM, Gwinn-Hardy K, Ro LS, Wang YC, Li SH, Hwang JC, Fang K, Hsieh-Li HM, Li ML, Tung LC, Su MT, Lu KT, Lee-Chen GJ.
    Clin Genet; 2004 Mar; 65(3):209-14. PubMed ID: 14756671
    [Abstract] [Full Text] [Related]

  • 26. 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]

  • 27. Clinical and molecular characteristics of a Brazilian family with spinocerebellar ataxia type 1.
    Lopes-Cendes I, Steiner CE, Silveira I, Pinto Júnior W, Maciel JA, Rouleau GA.
    Arq Neuropsiquiatr; 1996 Sep; 54(3):412-8. PubMed ID: 9109985
    [Abstract] [Full Text] [Related]

  • 28. 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]

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  • 30. Upward Gaze Palsy: a Valuable Sign to Distinguish Spinocerebellar Ataxias.
    Franklin GL, Meira AT, Camargo CHF, Nascimento FA, Teive HAG.
    Cerebellum; 2020 Oct 20; 19(5):685-690. PubMed ID: 32557336
    [Abstract] [Full Text] [Related]

  • 31. Brain pathology of spinocerebellar ataxias.
    Seidel K, Siswanto S, Brunt ER, den Dunnen W, Korf HW, Rüb U.
    Acta Neuropathol; 2012 Jul 20; 124(1):1-21. PubMed ID: 22684686
    [Abstract] [Full Text] [Related]

  • 32. 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]

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  • 34. [Spinocerebellar ataxias type 1 and 2: comparison of clinical, electrophysiological and magnetic resonance evaluation].
    Rakowicz M, Zdzienicka E, Poniatowska R, Waliniowska E, Sułek A, Jakubowska T, Niedzielska K, Rola R, Wierzbicka A, Hoffman-Zacharska D, Głazowski C, Jakubczyk T, Niewiadomska M, Zaremba J.
    Neurol Neurochir Pol; 2005 Sep 15; 39(4):263-275. PubMed ID: 16096942
    [Abstract] [Full Text] [Related]

  • 35. 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]

  • 36. Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion.
    Koutsis G, Karadima G, Pandraud A, Sweeney MG, Paudel R, Houlden H, Wood NW, Panas M.
    J Neurol; 2012 Sep 15; 259(9):1874-8. PubMed ID: 22297462
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  • 38. [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]

  • 39. Early-onset familial essential tremor is associated with nucleotide expansions of spinocerebellar ataxia in China.
    Zheng Z, Zhu Z, Pu J, Zhou C, Cao L, Lv D, Lu J, Zhao G, Chen Y, Tian J, Yin X, Zhang B, Yan Y, Zhao G.
    Mol Biol Rep; 2024 Jan 16; 51(1):113. PubMed ID: 38227102
    [Abstract] [Full Text] [Related]

  • 40. Screening for premutation in the FMR1 gene in male patients suspected of spinocerebellar ataxia.
    Rajkiewicz M, Sułek-Piatkowska A, Krysa W, Zdzienicka E, Szirkowiec W, Zaremba J.
    Neurol Neurochir Pol; 2008 Jan 16; 42(6):497-504. PubMed ID: 19235102
    [Abstract] [Full Text] [Related]

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