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405 related items for PubMed ID: 9403480

  • 1. 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
    [Abstract] [Full Text] [Related]

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

  • 3. Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1.
    Hashida H, Goto J, Kurisaki H, Mizusawa H, Kanazawa I.
    Ann Neurol; 1997 Apr; 41(4):505-11. PubMed ID: 9124808
    [Abstract] [Full Text] [Related]

  • 4. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
    Tang B, Xia J, Wang D, Tang X, Shen L, Liu C, Dai H, Yan X, Pan Q, Xiao J, Zhang B, Ou Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):281-4. PubMed ID: 10514531
    [Abstract] [Full Text] [Related]

  • 5. 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; 61(2):209-12. PubMed ID: 14967767
    [Abstract] [Full Text] [Related]

  • 6. Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease.
    Matilla T, McCall A, Subramony SH, Zoghbi HY.
    Ann Neurol; 1995 Jul; 38(1):68-72. PubMed ID: 7611728
    [Abstract] [Full Text] [Related]

  • 7. [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 Jul; 127(5-6):157-62. PubMed ID: 10500422
    [Abstract] [Full Text] [Related]

  • 8. Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.
    Nozaki H, Ikeuchi T, Kawakami A, Kimura A, Koide R, Tsuchiya M, Nakmura Y, Mutoh T, Yamamoto H, Nakao N, Sahashi K, Nishizawa M, Onodera O.
    Mov Disord; 2007 Apr 30; 22(6):857-62. PubMed ID: 17357132
    [Abstract] [Full Text] [Related]

  • 9. [Clinical, neuropathological and genetic characteristics of spinocerebellar ataxia type 6 (SCA6)].
    Ishikawa K, Mizusawa H.
    Nihon Rinsho; 1999 Apr 30; 57(4):880-5. PubMed ID: 10222783
    [Abstract] [Full Text] [Related]

  • 10. [Copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes].
    Chen P, Ma M, Shang H, Su D, Zhang S, Yang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec 30; 26(6):626-33. PubMed ID: 19953483
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.
    Dürr A, Stevanin G, Cancel G, Duyckaerts C, Abbas N, Didierjean O, Chneiweiss H, Benomar A, Lyon-Caen O, Julien J, Serdaru M, Penet C, Agid Y, Brice A.
    Ann Neurol; 1996 Apr 30; 39(4):490-9. PubMed ID: 8619527
    [Abstract] [Full Text] [Related]

  • 13. 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 30; 104(6):516-22. PubMed ID: 10453742
    [Abstract] [Full Text] [Related]

  • 14. [Spinocerebellar ataxia: advances in genetic research and its clinical implication].
    Sasaki H.
    Hokkaido Igaku Zasshi; 1997 Jan 30; 72(1):13-20. PubMed ID: 9086358
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Frequency analysis and clinical characterization of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Korean patients.
    Lee WY, Jin DK, Oh MR, Lee JE, Song SM, Lee EA, Kim GM, Chung JS, Lee KH.
    Arch Neurol; 2003 Jun 28; 60(6):858-63. PubMed ID: 12810491
    [Abstract] [Full Text] [Related]

  • 17. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
    Brusco A, Gellera C, Cagnoli C, Saluto A, Castucci A, Michielotto C, Fetoni V, Mariotti C, Migone N, Di Donato S, Taroni F.
    Arch Neurol; 2004 May 28; 61(5):727-33. PubMed ID: 15148151
    [Abstract] [Full Text] [Related]

  • 18. [Initial symptoms and mode of neurological progression in spinocerebellar ataxia type 6 (SCA6)].
    Yabe I, Sasaki H, Yamashita I, Takei A, Fukazawa T, Hamada T, Tashiro K.
    Rinsho Shinkeigaku; 1998 Jun 28; 38(6):489-94. PubMed ID: 9847664
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1.
    Goldfarb LG, Vasconcelos O, Platonov FA, Lunkes A, Kipnis V, Kononova S, Chabrashvili T, Vladimirtsev VA, Alexeev VP, Gajdusek DC.
    Ann Neurol; 1996 Apr 28; 39(4):500-6. PubMed ID: 8619528
    [Abstract] [Full Text] [Related]

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