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Journal Abstract Search

735 related items for PubMed ID: 10483966

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  • 2. Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.
    Zareba W, Moss AJ, Locati EH, Lehmann MH, Peterson DR, Hall WJ, Schwartz PJ, Vincent GM, Priori SG, Benhorin J, Towbin JA, Robinson JL, Andrews ML, Napolitano C, Timothy K, Zhang L, Medina A, International Long QT Syndrome Registry.
    J Am Coll Cardiol; 2003 Jul 02; 42(1):103-9. PubMed ID: 12849668
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  • 3. 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 02; 67(6):495-8. PubMed ID: 12808265
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  • 4. Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutations.
    Lupoglazoff JM, Denjoy I, Berthet M, Neyroud N, Demay L, Richard P, Hainque B, Vaksmann G, Klug D, Leenhardt A, Maillard G, Coumel P, Guicheney P.
    Circulation; 2001 Feb 27; 103(8):1095-101. PubMed ID: 11222472
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  • 6. Genotype- and mutation site-specific QT adaptation during exercise, recovery, and postural changes in children with long-QT syndrome.
    Aziz PF, Wieand TS, Ganley J, Henderson J, Patel AR, Iyer VR, Vogel RL, McBride M, Vetter VL, Shah MJ.
    Circ Arrhythm Electrophysiol; 2011 Dec 27; 4(6):867-73. PubMed ID: 21956039
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  • 13. [T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)].
    Lupoglazoff JM, Denjoy I, Berthet M, Hainque B, Vaksmann G, Klug D, Villain E, Lucet V, Guicheney P, Coumel P.
    Arch Mal Coeur Vaiss; 2001 May 27; 94(5):470-8. PubMed ID: 11434015
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  • 14. A new oral therapy for long QT syndrome: long-term oral potassium improves repolarization in patients with HERG mutations.
    Etheridge SP, Compton SJ, Tristani-Firouzi M, Mason JW.
    J Am Coll Cardiol; 2003 Nov 19; 42(10):1777-82. PubMed ID: 14642687
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  • 16. Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1).
    Wilde AA, Jongbloed RJ, Doevendans PA, Düren DR, Hauer RN, van Langen IM, van Tintelen JP, Smeets HJ, Meyer H, Geelen JL.
    J Am Coll Cardiol; 1999 Feb 19; 33(2):327-32. PubMed ID: 9973011
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  • 20. The inherited long QT syndrome: from ion channel to bedside.
    Vincent GM, Timothy K, Fox J, Zhang L.
    Cardiol Rev; 1999 Feb 19; 7(1):44-55. PubMed ID: 10348966
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