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Journal Abstract Search

387 related items for PubMed ID: 9550356

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  • 3. 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
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  • 7. Prevalence of spinocerebellar degenerations in the Hokuriku district in Japan.
    Shibata-Hamaguchi A, Ishida C, Iwasa K, Yamada M.
    Neuroepidemiology; 2009 Apr; 32(3):176-83. PubMed ID: 19169038
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  • 9. Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal.
    Vale J, Bugalho P, Silveira I, Sequeiros J, Guimarães J, Coutinho P.
    Eur J Neurol; 2010 Jan; 17(1):124-8. PubMed ID: 19659750
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  • 10. 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; 104(6):516-22. PubMed ID: 10453742
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  • 11. Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.
    Ikeuchi T, Takano H, Koide R, Horikawa Y, Honma Y, Onishi Y, Igarashi S, Tanaka H, Nakao N, Sahashi K, Tsukagoshi H, Inoue K, Takahashi H, Tsuji S.
    Ann Neurol; 1997 Dec; 42(6):879-84. PubMed ID: 9403480
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  • 12. 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; 58(7):1105-9. PubMed ID: 11448300
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  • 16. Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics.
    Whaley NR, Fujioka S, Wszolek ZK.
    Orphanet J Rare Dis; 2011 May 28; 6():33. PubMed ID: 21619691
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  • 17. Prevalence of autosomal dominant cerebellar ataxia in Aomori, the northernmost prefecture of Honshu, Japan.
    Yamamoto-Watanabe Y, Watanabe M, Hikichi M, Ikeda Y, Jackson M, Wakasaya Y, Matsubara E, Kawarabayashi T, Kannari K, Shoji M.
    Intern Med; 2010 May 28; 49(22):2409-14. PubMed ID: 21088341
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  • 18. Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds.
    Schöls L, Gispert S, Vorgerd M, Menezes Vieira-Saecker AM, Blanke P, Auburger G, Amoiridis G, Meves S, Epplen JT, Przuntek H, Pulst SM, Riess O.
    Arch Neurol; 1997 Sep 28; 54(9):1073-80. PubMed ID: 9311350
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  • 19. Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients.
    Lopes-Cendes I, Teive HG, Calcagnotto ME, Da Costa JC, Cardoso F, Viana E, Maciel JA, Radvany J, Arruda WO, Trevisol-Bittencourt PC, Rosa Neto P, Silveira I, Steiner CE, Pinto Júnior W, Santos AS, Correa Neto Y, Werneck LC, Araújo AQ, Carakushansky G, Mello LR, Jardim LB, Rouleau GA.
    Arq Neuropsiquiatr; 1997 Sep 28; 55(3B):519-29. PubMed ID: 9629399
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  • 20. Identification of five spinocerebellar ataxia type 2 pedigrees in patients with autosomal dominant cerebellar ataxia in Taiwan.
    Hsieh M, Li SY, Tsai CJ, Chen YY, Liu CS, Chang CY, Ro LS, Chen DF, Chen SS, Li C.
    Acta Neurol Scand; 1999 Sep 28; 100(3):189-94. PubMed ID: 10478584
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