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Journal Abstract Search

484 related items for PubMed ID: 9436730

  • 1. Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
    Schöls L, Krüger R, Amoiridis G, Przuntek H, Epplen JT, Riess O.
    J Neurol Neurosurg Psychiatry; 1998 Jan; 64(1):67-73. PubMed ID: 9436730
    [Abstract] [Full Text] [Related]

  • 2. 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; 6(8):1289-93. PubMed ID: 9259275
    [Abstract] [Full Text] [Related]

  • 3. 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; 54(9):1073-80. PubMed ID: 9311350
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 104(6):516-22. PubMed ID: 10453742
    [Abstract] [Full Text] [Related]

  • 7. Spinocerebellar ataxia type 6. Molecular and clinical features of 35 Japanese patients including one homozygous for the CAG repeat expansion.
    Matsumura R, Futamura N, Fujimoto Y, Yanagimoto S, Horikawa H, Suzumura A, Takayanagi T.
    Neurology; 1997 Nov 15; 49(5):1238-43. PubMed ID: 9371900
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 49(5):1243-6. PubMed ID: 9371901
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. [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
    [Abstract] [Full Text] [Related]

  • 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 15; 42(6):879-84. PubMed ID: 9403480
    [Abstract] [Full Text] [Related]

  • 12. The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.
    Giunti P, Sabbadini G, Sweeney MG, Davis MB, Veneziano L, Mantuano E, Federico A, Plasmati R, Frontali M, Wood NW.
    Brain; 1998 Mar 15; 121 ( Pt 3)():459-67. PubMed ID: 9549522
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6).
    Matsuyama Z, Kawakami H, Maruyama H, Izumi Y, Komure O, Udaka F, Kameyama M, Nishio T, Kuroda Y, Nishimura M, Nakamura S.
    Hum Mol Genet; 1997 Aug 28; 6(8):1283-7. PubMed ID: 9259274
    [Abstract] [Full Text] [Related]

  • 15. Frequency analysis of autosomal dominant cerebellar ataxias in Japanese patients and clinical characterization of spinocerebellar ataxia type 6.
    Watanabe H, Tanaka F, Matsumoto M, Doyu M, Ando T, Mitsuma T, Sobue G.
    Clin Genet; 1998 Jan 28; 53(1):13-9. PubMed ID: 9550356
    [Abstract] [Full Text] [Related]

  • 16. 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 28; 98(1):55-9. PubMed ID: 9696528
    [Abstract] [Full Text] [Related]

  • 17. [Molecular and clinical features in spinocerebellar ataxia type 6 (SCA6) in Japanese].
    Ikeuchi T.
    Nihon Rinsho; 1999 Apr 28; 57(4):891-5. PubMed ID: 10222785
    [Abstract] [Full Text] [Related]

  • 18. Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA6).
    Sasaki H, Kojima H, Yabe I, Tashiro K, Hamada T, Sawa H, Hiraga H, Nagashima K.
    Acta Neuropathol; 1998 Feb 28; 95(2):199-204. PubMed ID: 9498057
    [Abstract] [Full Text] [Related]

  • 19. [Clinico-genetic study of type I spinocerebelllar ataxia].
    Svetel M, Culjković B, Sternić N, Dragasević B, Stojković I, Romac S, Kostić VS.
    Srp Arh Celok Lek; 1999 Feb 28; 127(5-6):157-62. PubMed ID: 10500422
    [Abstract] [Full Text] [Related]

  • 20. Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.
    Ishikawa K, Tanaka H, Saito M, Ohkoshi N, Fujita T, Yoshizawa K, Ikeuchi T, Watanabe M, Hayashi A, Takiyama Y, Nishizawa M, Nakano I, Matsubayashi K, Miwa M, Shoji S, Kanazawa I, Tsuji S, Mizusawa H.
    Am J Hum Genet; 1997 Aug 28; 61(2):336-46. PubMed ID: 9311738
    [Abstract] [Full Text] [Related]

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