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Journal Abstract Search

570 related items for PubMed ID: 14767919

  • 1. [Analysis and application of SCA1 and SCA3/MJD gene CAG repeats in Han population in Northeastern China].
    Jiang M, Jin CL, Lin CK, Qiu GR, Liu ZL, Wang CX, Sun KL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):83-5. PubMed ID: 14767919
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  • 3. [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; 77(11):819-22. PubMed ID: 9772474
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  • 4. 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; 109(5):355-60. PubMed ID: 15080863
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  • 6. [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; 31(5):702-5. PubMed ID: 17062934
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  • 8. 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
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  • 9. 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
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  • 10. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia.
    Geschwind DH, Perlman S, Figueroa CP, Treiman LJ, Pulst SM.
    Am J Hum Genet; 1997 Apr 28; 60(4):842-50. PubMed ID: 9106530
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  • 12. Spinocerebellar ataxias types 1, 2 and 3: age adjusted clinical severity of disease at presentation correlates with size of CAG repeat lengths.
    Netravathi M, Pal PK, Purushottam M, Thennarasu K, Mukherjee M, Jain S.
    J Neurol Sci; 2009 Feb 15; 277(1-2):83-6. PubMed ID: 19049837
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  • 14. Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic.
    Wang YG, Du J, Wang JL, Chen J, Chen C, Luo YY, Xiao ZQ, Jiang H, Yan XX, Xia K, Pan Q, Tang BS, Shen L.
    J Neurol Sci; 2009 Oct 15; 285(1-2):121-4. PubMed ID: 19608203
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  • 15. [Clinical features and gene mutation analysis in Machado-Joseph disease of spinocerebellar ataxia type 3 in littoral of Zhejiang].
    Jin YY, Zeng AP, Cai HB, Wu F, Feng Z, Hong Q, Zhang L, Jiang ZK.
    Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi; 2009 Apr 15; 23(2):132-4. PubMed ID: 20104758
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