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Journal Abstract Search

259 related items for PubMed ID: 9696528

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

  • 2. 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]

  • 3. 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
    [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. 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; 61(5):727-33. PubMed ID: 15148151
    [Abstract] [Full Text] [Related]

  • 6. Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India.
    Basu P, Chattopadhyay B, Gangopadhaya PK, Mukherjee SC, Sinha KK, Das SK, Roychoudhury S, Majumder PP, Bhattacharyya NP.
    Hum Genet; 2000 Jun; 106(6):597-604. PubMed ID: 10942107
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 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 28; 42(6):879-84. PubMed ID: 9403480
    [Abstract] [Full Text] [Related]

  • 9. [SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].
    Tang B, Wang D, Xia J.
    Zhonghua Yi Xue Za Zhi; 1997 Nov 28; 77(11):819-22. PubMed ID: 9772474
    [Abstract] [Full Text] [Related]

  • 10. 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 28; 49(5):1238-43. PubMed ID: 9371900
    [Abstract] [Full Text] [Related]

  • 11. Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families.
    Filla A, Mariotti C, Caruso G, Coppola G, Cocozza S, Castaldo I, Calabrese O, Salvatore E, De Michele G, Riggio MC, Pareyson D, Gellera C, Di Donato S.
    Eur Neurol; 2000 Nov 28; 44(1):31-6. PubMed ID: 10894992
    [Abstract] [Full Text] [Related]

  • 12. 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 28; 6(8):1289-93. PubMed ID: 9259275
    [Abstract] [Full Text] [Related]

  • 13. Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan.
    Tsai HF, Liu CS, Leu TM, Wen FC, Lin SJ, Liu CC, Yang DK, Li C, Hsieh M.
    Acta Neurol Scand; 2004 May 28; 109(5):355-60. PubMed ID: 15080863
    [Abstract] [Full Text] [Related]

  • 14. 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 28; 64(1):67-73. PubMed ID: 9436730
    [Abstract] [Full Text] [Related]

  • 15. [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]

  • 16. Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.
    Leggo J, Dalton A, Morrison PJ, Dodge A, Connarty M, Kotze MJ, Rubinsztein DC.
    J Med Genet; 1997 Dec 28; 34(12):982-5. PubMed ID: 9429138
    [Abstract] [Full Text] [Related]

  • 17. Frequency of spinocerebellar ataxia mutations in the Kinki district of Japan.
    Matsumura R, Futamura N, Ando N, Ueno S.
    Acta Neurol Scand; 2003 Jan 28; 107(1):38-41. PubMed ID: 12542511
    [Abstract] [Full Text] [Related]

  • 18. 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 28; 61(2):209-12. PubMed ID: 14967767
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 20. [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 Sep 28; 127(5-6):157-62. PubMed ID: 10500422
    [Abstract] [Full Text] [Related]

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