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Journal Abstract Search

514 related items for PubMed ID: 9429138

  • 1. 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; 34(12):982-5. PubMed ID: 9429138
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

  • 4. 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]

  • 5. 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]

  • 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 28; 106(6):597-604. PubMed ID: 10942107
    [Abstract] [Full Text] [Related]

  • 7. [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]

  • 8. Molecular analysis of Spinocerebellar ataxias in Koreans: frequencies and reference ranges of SCA1, SCA2, SCA3, SCA6, and SCA7.
    Kim JY, Park SS, Joo SI, Kim JM, Jeon BS.
    Mol Cells; 2001 Dec 31; 12(3):336-41. PubMed ID: 11804332
    [Abstract] [Full Text] [Related]

  • 9. 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 31; 109(5):355-60. PubMed ID: 15080863
    [Abstract] [Full Text] [Related]

  • 10. A genetic epidemiological study of spinocerebellar ataxias in Tottori prefecture, Japan.
    Mori M, Adachi Y, Kusumi M, Nakashima K.
    Neuroepidemiology; 2001 May 31; 20(2):144-9. PubMed ID: 11359084
    [Abstract] [Full Text] [Related]

  • 11. 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 31; 63(4):1060-6. PubMed ID: 9758625
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Spinocerebellar ataxias in mainland China: an updated genetic analysis among a large cohort of familial and sporadic cases.
    Wang J, Shen L, Lei L, Xu Q, Zhou J, Liu Y, Guan W, Pan Q, Xia K, Tang B, Jiang H.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2011 Jun 08; 36(6):482-9. PubMed ID: 21743138
    [Abstract] [Full Text] [Related]

  • 14. Friedreich's ataxia and other hereditary ataxias in Greece: an 18-year perspective.
    Koutsis G, Kladi A, Karadima G, Houlden H, Wood NW, Christodoulou K, Panas M.
    J Neurol Sci; 2014 Jan 15; 336(1-2):87-92. PubMed ID: 24209901
    [Abstract] [Full Text] [Related]

  • 15. The expansion of the CAG repeat in ataxin-2 is a frequent cause of autosomal dominant spinocerebellar ataxia.
    Lorenzetti D, Bohlega S, Zoghbi HY.
    Neurology; 1997 Oct 15; 49(4):1009-13. PubMed ID: 9339681
    [Abstract] [Full Text] [Related]

  • 16. The occurrence of dominant spinocerebellar ataxias among 251 Finnish ataxia patients and the role of predisposing large normal alleles in a genetically isolated population.
    Juvonen V, Hietala M, Kairisto V, Savontaus ML.
    Acta Neurol Scand; 2005 Mar 15; 111(3):154-62. PubMed ID: 15691283
    [Abstract] [Full Text] [Related]

  • 17. [Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China].
    Song XW, Tang BS, Jiang H, Shen L, Yang Q, Liao SS, Li QH, Tang JG.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2006 Oct 15; 31(5):702-5. PubMed ID: 17062934
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 98(1):55-9. PubMed ID: 9696528
    [Abstract] [Full Text] [Related]

  • 19. The occurrence of spinocerebellar ataxias caused by dynamic mutations in Polish patients.
    Sułek-Piatkowska A, Zdzienicka E, Raczyńska-Rakowicz M, Krysa W, Rajkiewicz M, Szirkowiec W, Zaremba J.
    Neurol Neurochir Pol; 2010 Jul 15; 44(3):238-45. PubMed ID: 20625959
    [Abstract] [Full Text] [Related]

  • 20. Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families.
    Moseley ML, Benzow KA, Schut LJ, Bird TD, Gomez CM, Barkhaus PE, Blindauer KA, Labuda M, Pandolfo M, Koob MD, Ranum LP.
    Neurology; 1998 Dec 15; 51(6):1666-71. PubMed ID: 9855520
    [Abstract] [Full Text] [Related]

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