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Journal Abstract Search

523 related items for PubMed ID: 12849668

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  • 5. Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG.
    Inoue M, Shimizu M, Ino H, Yamaguchi M, Terai H, Hayashi K, Kiyama M, Sakata K, Hayashi T, Mabuchi H.
    Circ J; 2003 Jun; 67(6):495-8. PubMed ID: 12808265
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  • 7. The long QT syndrome: new diagnostic and therapeutic approach in the era of molecular biology.
    Priori SG, Cantù F, Schwartz PJ.
    Schweiz Med Wochenschr; 1996 Oct 12; 126(41):1727-31. PubMed ID: 8893413
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  • 9. Variable expression of long QT syndrome among gene carriers from families with five different HERG mutations.
    Benhorin J, Moss AJ, Bak M, Zareba W, Kaufman ES, Kerem B, Towbin JA, Priori S, Kass RS, Attali B, Brown AM, Ficker E.
    Ann Noninvasive Electrocardiol; 2002 Jan 12; 7(1):40-6. PubMed ID: 11844290
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  • 14. Association of long QT syndrome loci and cardiac events among patients treated with beta-blockers.
    Priori SG, Napolitano C, Schwartz PJ, Grillo M, Bloise R, Ronchetti E, Moncalvo C, Tulipani C, Veia A, Bottelli G, Nastoli J.
    JAMA; 2004 Sep 15; 292(11):1341-4. PubMed ID: 15367556
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  • 15. The inherited long QT syndrome: from ion channel to bedside.
    Vincent GM, Timothy K, Fox J, Zhang L.
    Cardiol Rev; 1999 Sep 15; 7(1):44-55. PubMed ID: 10348966
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  • 16. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
    Vincent GM.
    Annu Rev Med; 1998 Sep 15; 49():263-74. PubMed ID: 9509262
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