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Journal Abstract Search

375 related items for PubMed ID: 19938636

  • 1.
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  • 3. Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease.
    Agostinho Lde A, Rocha CF, Medina-Acosta E, Barboza HN, da Silva AF, Pereira SP, da Silva Idos S, Paradela ER, Figueiredo AL, Nogueira Ede M, Alvarenga RM, Hernan Cabello P, dos Santos SR, Paiva CL.
    J Hum Genet; 2012 Dec; 57(12):796-803. PubMed ID: 23051704
    [Abstract] [Full Text] [Related]

  • 4. Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population.
    Ma M, Yang Y, Shang H, Su D, Zhang H, Ma Y, Liu Y, Tao D, Zhang S.
    J Neurol Sci; 2010 Nov 15; 298(1-2):57-60. PubMed ID: 20864123
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  • 6. Intergeneration CAG expansion and contraction in a Chinese HD family.
    Tang Y, Wang Y, Yang P, Liu Y, Wang B, Podolsky R, McIndoe R, Wang CY.
    Am J Med Genet B Neuropsychiatr Genet; 2006 Apr 05; 141B(3):242-4. PubMed ID: 16526033
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  • 7. [From gene to disease; HD gene and Huntington disease].
    Maat-Kievit JA, Losekoot M, Roos RA.
    Ned Tijdschr Geneeskd; 2001 Nov 03; 145(44):2120-3. PubMed ID: 11723754
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  • 8. Autopsy-proven Huntington's disease with 29 trinucleotide repeats.
    Kenney C, Powell S, Jankovic J.
    Mov Disord; 2007 Jan 03; 22(1):127-30. PubMed ID: 17115386
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  • 9. [Analysis of the IT15 gene in Huntington's disease families].
    Genetika; 2004 Aug 03; 40(8):1123-30. PubMed ID: 15523851
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  • 10. Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease.
    Masuda N, Goto J, Murayama N, Watanabe M, Kondo I, Kanazawa I.
    J Med Genet; 1995 Sep 03; 32(9):701-5. PubMed ID: 8544189
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  • 11. Analysis of CCG repeats in Huntingtin gene among HD patients and normal populations in Japan.
    Morovvati S, Nakagawa M, Osame M, Karami A.
    Arch Med Res; 2008 Jan 03; 39(1):131-3. PubMed ID: 18068007
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  • 12. [Genetic diagnosis of Huntington disease].
    Mo YQ, Li LY, Lu GX.
    Yi Chuan; 2005 Nov 03; 27(6):861-4. PubMed ID: 16378928
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  • 13. The number of CAG repeats within the normal allele does not influence the age of onset in Huntington's disease.
    Klempíř J, Zidovská J, Stochl J, Ing VK, Uhrová T, Roth J.
    Mov Disord; 2011 Jan 03; 26(1):125-9. PubMed ID: 21322024
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  • 14. [Clinical characteristics of Huntington disease in two pedigrees and analysis of expanded CAG trinucleotide repeat].
    Cao GN, Bao XH, Lu HM, Zhang JJ, Ma YN, Gu WH, Xiong H, Qin J, Wu XR.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2011 Apr 18; 43(2):163-7. PubMed ID: 21503105
    [Abstract] [Full Text] [Related]

  • 15. Huntington's Disease: Relationship Between Phenotype and Genotype.
    Sun YM, Zhang YB, Wu ZY.
    Mol Neurobiol; 2017 Jan 18; 54(1):342-348. PubMed ID: 26742514
    [Abstract] [Full Text] [Related]

  • 16. Parent-of-origin differences of mutant HTT CAG repeat instability in Huntington's disease.
    Aziz NA, van Belzen MJ, Coops ID, Belfroid RD, Roos RA.
    Eur J Med Genet; 2011 Jan 18; 54(4):e413-8. PubMed ID: 21540131
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  • 17. Intergeneration CAG expansion in a Wuhan juvenile-onset Huntington disease family.
    Liu Y, Shen Y, Li H, Wang H, Yang ZR, Chen Y, Tang YP.
    Neurosci Bull; 2007 Jul 18; 23(4):198-202. PubMed ID: 17687393
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  • 18. Glutathione S-Transferase Omega 1 variation does not influence age at onset of Huntington's disease.
    Arning L, Jagiello P, Wieczorek S, Saft C, Andrich J, Epplen JT.
    BMC Med Genet; 2004 Mar 24; 5():7. PubMed ID: 15040808
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  • 19. Chorea Huntington: a rare case with childhood onset.
    Gencik M, Hammans C, Strehl H, Wagner N, Epplen JT.
    Neuropediatrics; 2002 Apr 24; 33(2):90-2. PubMed ID: 12075490
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  • 20. Age at onset in Huntington's disease: replication study on the association of HAP1.
    Karadima G, Dimovasili C, Koutsis G, Vassilopoulos D, Panas M.
    Parkinsonism Relat Disord; 2012 Nov 24; 18(9):1027-8. PubMed ID: 22698993
    [Abstract] [Full Text] [Related]

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