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Journal Abstract Search

188 related items for PubMed ID: 11804332

  • 1. 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
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  • 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 31; 61(5):727-33. PubMed ID: 15148151
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  • 5. 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
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  • 6. 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 31; 104(6):516-22. PubMed ID: 10453742
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  • 7. 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 Jun 31; 44(3):238-45. PubMed ID: 20625959
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  • 10. 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
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  • 12. [The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7].
    Yin XZ, Zhang BR, Wu DW, Tian J, Zhang H.
    Yi Chuan; 2007 Jun 08; 29(6):688-92. PubMed ID: 17650485
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  • 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
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  • 14. The hereditary adult-onset ataxias in South Africa.
    Bryer A, Krause A, Bill P, Davids V, Bryant D, Butler J, Heckmann J, Ramesar R, Greenberg J.
    J Neurol Sci; 2003 Dec 15; 216(1):47-54. PubMed ID: 14607302
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  • 15. [Studies on the CAG repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese Han].
    Wang J, Xu Q, Lei L, Shen L, Jiang H, Li X, Zhou Y, Yi J, Zhou J, Yan X, Pan Q, Xia K, Tang B.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec 15; 26(6):620-5. PubMed ID: 19953482
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  • 16. A genetic epidemiological study of spinocerebellar ataxias in Tottori prefecture, Japan.
    Mori M, Adachi Y, Kusumi M, Nakashima K.
    Neuroepidemiology; 2001 May 15; 20(2):144-9. PubMed ID: 11359084
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  • 17. 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
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  • 18. 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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  • 19. Diagnosis of five spinocerebellar ataxia disorders by multiplex amplification and capillary electrophoresis.
    Dorschner MO, Barden D, Stephens K.
    J Mol Diagn; 2002 May 15; 4(2):108-13. PubMed ID: 11986402
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