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Journal Abstract Search

405 related items for PubMed ID: 9403480

  • 41.
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  • 42. Age at onset variance analysis in spinocerebellar ataxias: a study in a Dutch-French cohort.
    van de Warrenburg BP, Hendriks H, Dürr A, van Zuijlen MC, Stevanin G, Camuzat A, Sinke RJ, Brice A, Kremer BP.
    Ann Neurol; 2005 Apr; 57(4):505-12. PubMed ID: 15747371
    [Abstract] [Full Text] [Related]

  • 43. The effect of CAT trinucleotide interruptions on the age at onset of spinocerebellar ataxia type 1 (SCA1).
    Matsuyama Z, Izumi Y, Kameyama M, Kawakami H, Nakamura S.
    J Med Genet; 1999 Jul; 36(7):546-8. PubMed ID: 10424816
    [Abstract] [Full Text] [Related]

  • 44. Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations.
    Takano H, Cancel G, Ikeuchi T, Lorenzetti D, Mawad R, Stevanin G, Didierjean O, Dürr A, Oyake M, Shimohata T, Sasaki R, Koide R, Igarashi S, Hayashi S, Takiyama Y, Nishizawa M, Tanaka H, Zoghbi H, Brice A, Tsuji S.
    Am J Hum Genet; 1998 Oct; 63(4):1060-6. PubMed ID: 9758625
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  • 45.
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  • 46. Uncloned expanded CAG/CTG repeat sequences in autosomal dominant cerebellar ataxia (ADCA) detected by the repeat expansion detection (RED) method.
    Pujana MA, Volpini V, Gratacós M, Corral J, Banchs I, Sánchez A, Genís D, Cervera C, Estivill X.
    J Med Genet; 1998 Feb; 35(2):99-102. PubMed ID: 9507387
    [Abstract] [Full Text] [Related]

  • 47.
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  • 48. 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; 61(2):336-46. PubMed ID: 9311738
    [Abstract] [Full Text] [Related]

  • 49. Expanded CAG repeats in spinocerebellar ataxia (SCA1) segregate with distinct haplotypes in South african families.
    Ramesar RS, Bardien S, Beighton P, Bryer A.
    Hum Genet; 1997 Jul; 100(1):131-7. PubMed ID: 9225982
    [Abstract] [Full Text] [Related]

  • 50. [Clinical and genetic characteristics of SCA1].
    Abe K.
    Nihon Rinsho; 1999 Apr; 57(4):796-800. PubMed ID: 10222768
    [Abstract] [Full Text] [Related]

  • 51. 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; 53(1):13-9. PubMed ID: 9550356
    [Abstract] [Full Text] [Related]

  • 52.
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  • 53.
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  • 54. [The phenotype variation correlates with the size of CAG repeat in SCA2].
    Sasaki H, Sanpei K.
    Nihon Rinsho; 1999 Apr; 57(4):818-21. PubMed ID: 10222772
    [Abstract] [Full Text] [Related]

  • 55. The repeat expansion detection method in the analysis of diseases with CAG/CTG repeat expansion: usefulness and limitations.
    Martorell L, Pujana MA, Volpini V, Sanchez A, Joven J, Vilella E, Estivill X.
    Hum Mutat; 1997 Apr; 10(6):486-8. PubMed ID: 9401013
    [Abstract] [Full Text] [Related]

  • 56. 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]

  • 57. Long-term disability and prognosis in dentatorubral-pallidoluysian atrophy: a correlation with CAG repeat length.
    Hasegawa A, Ikeuchi T, Koike R, Matsubara N, Tsuchiya M, Nozaki H, Homma A, Idezuka J, Nishizawa M, Onodera O.
    Mov Disord; 2010 Aug 15; 25(11):1694-700. PubMed ID: 20589872
    [Abstract] [Full Text] [Related]

  • 58. Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients.
    Maruyama H, Izumi Y, Morino H, Oda M, Toji H, Nakamura S, Kawakami H.
    Am J Med Genet; 2002 Jul 08; 114(5):578-83. PubMed ID: 12116198
    [Abstract] [Full Text] [Related]

  • 59. 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 08; 49(5):1243-6. PubMed ID: 9371901
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  • 60.
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