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Journal Abstract Search

216 related items for PubMed ID: 12808265

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  • 3. 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. Multi-undulant T-U-wave, sinus bradycardia and long QT syndrome: a possible phenotype of mutant genes controlling the inward potassium rectifiers.
    Shen CT, Wu YC, Yu SS, Wang NK.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997 Feb 27; 38(4):267-75. PubMed ID: 9297927
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  • 8. Non-invasive testing of acquired long QT syndrome: evidence for multiple arrhythmogenic substrates.
    Chevalier P, Rodriguez C, Bontemps L, Miquel M, Kirkorian G, Rousson R, Potet F, Schott JJ, Baró I, Touboul P.
    Cardiovasc Res; 2001 May 27; 50(2):386-98. PubMed ID: 11334843
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  • 9. KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
    Liu W, Yang J, Hu D, Kang C, Li C, Zhang S, Li P, Chen Z, Qin X, Ying K, Li Y, Li Y, Li Z, Cheng X, Li L, Qi Y, Chen S, Wang Q.
    Hum Mutat; 2002 Dec 27; 20(6):475-6. PubMed ID: 12442276
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  • 10. The long QT syndromes: genetic basis and clinical implications.
    Chiang CE, Roden DM.
    J Am Coll Cardiol; 2000 Jul 27; 36(1):1-12. PubMed ID: 10898405
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  • 12. The inherited long QT syndrome: from ion channel to bedside.
    Vincent GM, Timothy K, Fox J, Zhang L.
    Cardiol Rev; 1999 Jul 27; 7(1):44-55. PubMed ID: 10348966
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  • 14. Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndrome.
    Moennig G, Schulze-Bahr E, Wedekind H, Borggrefe M, Funke H, Toelle M, Kirchhof P, Eckardt L, Assmann G, Breithardt G, Haverkamp W.
    Pacing Clin Electrophysiol; 2001 Apr 27; 24(4 Pt 1):406-15. PubMed ID: 11341076
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  • 15. The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome.
    Van Langen IM, Birnie E, Alders M, Jongbloed RJ, Le Marec H, Wilde AA.
    J Med Genet; 2003 Feb 27; 40(2):141-5. PubMed ID: 12566525
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  • 17. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
    Vincent GM.
    Annu Rev Med; 1998 Feb 27; 49():263-74. PubMed ID: 9509262
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  • 18. 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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