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Journal Abstract Search

268 related items for PubMed ID: 20400777

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  • 3. Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population.
    Gouas L, Nicaud V, Berthet M, Forhan A, Tiret L, Balkau B, Guicheney P, D.E.S.I.R. Study Group.
    Eur J Hum Genet; 2005 Nov; 13(11):1213-22. PubMed ID: 16132053
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  • 9. Genetic variation in the rhythmonome: ethnic variation and haplotype structure in candidate genes for arrhythmias.
    Bush WS, Crawford DC, Alexander C, George AL, Roden DM, Ritchie MD.
    Pharmacogenomics; 2009 Jun; 10(6):1043-53. PubMed ID: 19530973
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  • 11. Mutation screening in KCNQ1, HERG, KCNE1, KCNE2 and SCN5A genes in a long QT syndrome family.
    Koo SH, Teo WS, Ching CK, Chan SH, Lee EJ.
    Ann Acad Med Singap; 2007 Jun; 36(6):394-8. PubMed ID: 17597962
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  • 12. Relationship between genetic variants in myocardial sodium and potassium channel genes and QT interval duration in diabetics: the Diabetes Heart Study.
    Lehtinen AB, Daniel KR, Shah SA, Nelson MR, Ziegler JT, Freedman BI, Carr JJ, Herrington DM, Langefeld CD, Bowden DW.
    Ann Noninvasive Electrocardiol; 2009 Jan; 14(1):72-9. PubMed ID: 19149796
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  • 15. [KCNQ1, KCNH2, KCNE1 and KCNE2 potassium channels gene variants in sudden manhood death syndrome].
    Zhao QH, Liu C, Lu LW, Lü GL, Liu H, Tang SB, Quan L, Cheng JD.
    Fa Yi Xue Za Zhi; 2012 Oct; 28(5):337-41, 346. PubMed ID: 23213782
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  • 16. Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.
    Barc J, Briec F, Schmitt S, Kyndt F, Le Cunff M, Baron E, Vieyres C, Sacher F, Redon R, Le Caignec C, Le Marec H, Probst V, Schott JJ.
    J Am Coll Cardiol; 2011 Jan 04; 57(1):40-7. PubMed ID: 21185499
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  • 17. Investigation of ion channel gene variants in patients with long QT syndrome.
    Ernesto C, Cruz FE, Lima FS, Coutinho JL, Silva R, Urményi TP, Carvalho AC, Rondinelli E.
    Arq Bras Cardiol; 2011 Mar 04; 96(3):172-8. PubMed ID: 21308345
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  • 18. Associations between common ion channel single nucleotide polymorphisms and sudden cardiac death in adults: A MOOSE-compliant meta-analysis.
    Liu X, Shi J, Xiao P.
    Medicine (Baltimore); 2018 Sep 04; 97(38):e12428. PubMed ID: 30235722
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  • 19. Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
    Kapplinger JD, Tester DJ, Salisbury BA, Carr JL, Harris-Kerr C, Pollevick GD, Wilde AA, Ackerman MJ.
    Heart Rhythm; 2009 Sep 04; 6(9):1297-303. PubMed ID: 19716085
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  • 20. Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths.
    Wang D, Shah KR, Um SY, Eng LS, Zhou B, Lin Y, Mitchell AA, Nicaj L, Prinz M, McDonald TV, Sampson BA, Tang Y.
    Forensic Sci Int; 2014 Apr 04; 237():90-9. PubMed ID: 24631775
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