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Journal Abstract Search

444 related items for PubMed ID: 19843919

  • 1. Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome.
    Itoh H, Sakaguchi T, Ding WG, Watanabe E, Watanabe I, Nishio Y, Makiyama T, Ohno S, Akao M, Higashi Y, Zenda N, Kubota T, Mori C, Okajima K, Haruna T, Miyamoto A, Kawamura M, Ishida K, Nagaoka I, Oka Y, Nakazawa Y, Yao T, Jo H, Sugimoto Y, Ashihara T, Hayashi H, Ito M, Imoto K, Matsuura H, Horie M.
    Circ Arrhythm Electrophysiol; 2009 Oct; 2(5):511-23. PubMed ID: 19843919
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  • 2. Atrioventricular block-induced Torsades de Pointes with clinical and molecular backgrounds similar to congenital long QT syndrome.
    Oka Y, Itoh H, Ding WG, Shimizu W, Makiyama T, Ohno S, Nishio Y, Sakaguchi T, Miyamoto A, Kawamura M, Matsuura H, Horie M.
    Circ J; 2010 Nov; 74(12):2562-71. PubMed ID: 20975234
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  • 3. Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients.
    Paulussen AD, Gilissen RA, Armstrong M, Doevendans PA, Verhasselt P, Smeets HJ, Schulze-Bahr E, Haverkamp W, Breithardt G, Cohen N, Aerssens J.
    J Mol Med (Berl); 2004 Mar; 82(3):182-8. PubMed ID: 14760488
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  • 5. Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative results.
    Tester DJ, Cronk LB, Carr JL, Schulz V, Salisbury BA, Judson RS, Ackerman MJ.
    Heart Rhythm; 2006 Jul; 3(7):815-21. PubMed ID: 16818214
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  • 9. Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome.
    Grunnet M, Behr ER, Calloe K, Hofman-Bang J, Till J, Christiansen M, McKenna WJ, Olesen SP, Schmitt N.
    Heart Rhythm; 2005 Nov; 2(11):1238-49. PubMed ID: 16253915
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  • 10. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
    Vincent GM.
    Annu Rev Med; 1998 Nov; 49():263-74. PubMed ID: 9509262
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  • 17. QT interval prolongation and cardiac risk assessment for novel drugs.
    Picard S, Lacroix P.
    Curr Opin Investig Drugs; 2003 Mar; 4(3):303-8. PubMed ID: 12735231
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  • 18. 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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  • 20. Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients.
    Chang YS, Yang YW, Lin YN, Lin KH, Chang KC, Chang JG.
    Int Heart J; 2015 Jun; 56(4):450-3. PubMed ID: 26118593
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