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PUBMED FOR HANDHELDS

Journal Abstract Search


274 related items for PubMed ID: 9371900

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  • 3. CAG repeat expansions in patients with sporadic cerebellar ataxia.
    Futamura N, Matsumura R, Fujimoto Y, Horikawa H, Suzumura A, Takayanagi T.
    Acta Neurol Scand; 1998 Jul; 98(1):55-9. PubMed ID: 9696528
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  • 5. Clinical and molecular features of spinocerebellar ataxia type 6.
    Stevanin G, Dürr A, David G, Didierjean O, Cancel G, Rivaud S, Tourbah A, Warter JM, Agid Y, Brice A.
    Neurology; 1997 Nov; 49(5):1243-6. PubMed ID: 9371901
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  • 7. A Japanese family with spinocerebellar ataxia type 6 which includes three individuals homozygous for an expanded CAG repeat in the SCA6/CACNL1A4 gene.
    Takiyama Y, Sakoe K, Namekawa M, Soutome M, Esumi E, Ogawa T, Ishikawa K, Mizusawa H, Nakano I, Nishizawa M.
    J Neurol Sci; 1998 Jun 30; 158(2):141-7. PubMed ID: 9702684
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  • 8. 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 30; 42(6):879-84. PubMed ID: 9403480
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  • 9. SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene.
    Riess O, Schöls L, Bottger H, Nolte D, Vieira-Saecker AM, Schimming C, Kreuz F, Macek M, Krebsová A, Macek M Sen, Klockgether T, Zühlke C, Laccone FA.
    Hum Mol Genet; 1997 Aug 30; 6(8):1289-93. PubMed ID: 9259275
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  • 10. Clinical and molecular genetic study in seven Japanese families with spinocerebellar ataxia type 6.
    Nagai Y, Azuma T, Funauchi M, Fujita M, Umi M, Hirano M, Matsubara T, Ueno S.
    J Neurol Sci; 1998 Apr 15; 157(1):52-9. PubMed ID: 9600677
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  • 11. Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations.
    Geschwind DH, Perlman S, Figueroa KP, Karrim J, Baloh RW, Pulst SM.
    Neurology; 1997 Nov 15; 49(5):1247-51. PubMed ID: 9371902
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  • 12. Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotype.
    Benton CS, de Silva R, Rutledge SL, Bohlega S, Ashizawa T, Zoghbi HY.
    Neurology; 1998 Oct 15; 51(4):1081-6. PubMed ID: 9781533
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  • 15. [Clinical, neuropathological and genetic characteristics of spinocerebellar ataxia type 6 (SCA6)].
    Ishikawa K, Mizusawa H.
    Nihon Rinsho; 1999 Apr 15; 57(4):880-5. PubMed ID: 10222783
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  • 16. Clinical and molecular correlations in spinocerebellar ataxia type 6: a study of 24 Dutch families.
    Sinke RJ, Ippel EF, Diepstraten CM, Beemer FA, Wokke JH, van Hilten BJ, Knoers NV, van Amstel HK, Kremer HP.
    Arch Neurol; 2001 Nov 15; 58(11):1839-44. PubMed ID: 11708993
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  • 17. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
    Oda M, Maruyama H, Komure O, Morino H, Terasawa H, Izumi Y, Imamura T, Yasuda M, Ichikawa K, Ogawa M, Matsumoto M, Kawakami H.
    Arch Neurol; 2004 Feb 15; 61(2):209-12. PubMed ID: 14967767
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  • 18. Sisters homozygous for the spinocerebellar ataxia type 6 (SCA6)/CACNA1A gene associated with different clinical phenotypes.
    Kato T, Tanaka F, Yamamoto M, Yosida E, Indo T, Watanabe H, Yoshiwara T, Doyu M, Sobue G.
    Clin Genet; 2000 Jul 15; 58(1):69-73. PubMed ID: 10945665
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  • 19. Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p.
    Jodice C, Mantuano E, Veneziano L, Trettel F, Sabbadini G, Calandriello L, Francia A, Spadaro M, Pierelli F, Salvi F, Ophoff RA, Frants RR, Frontali M.
    Hum Mol Genet; 1997 Oct 15; 6(11):1973-8. PubMed ID: 9302278
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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 15; 100(3):189-94. PubMed ID: 10478584
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