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Journal Abstract Search

372 related items for PubMed ID: 15367556

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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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  • 4. Utility of treadmill testing in identification and genotype prediction in long-QT syndrome.
    Wong JA, Gula LJ, Klein GJ, Yee R, Skanes AC, Krahn AD.
    Circ Arrhythm Electrophysiol; 2010 Apr 02; 3(2):120-5. PubMed ID: 20071715
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  • 5. Molecular biology of the long QT syndrome: impact on management.
    Priori SG, Napolitano C, Paganini V, Cantù F, Schwartz PJ.
    Pacing Clin Electrophysiol; 1997 Aug 02; 20(8 Pt 2):2052-7. PubMed ID: 9272507
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  • 6. The long QT syndromes: genetic basis and clinical implications.
    Chiang CE, Roden DM.
    J Am Coll Cardiol; 2000 Jul 02; 36(1):1-12. PubMed ID: 10898405
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  • 8. The inherited long QT syndrome: from ion channel to bedside.
    Vincent GM, Timothy K, Fox J, Zhang L.
    Cardiol Rev; 1999 Jul 02; 7(1):44-55. PubMed ID: 10348966
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  • 11. Atrial Fibrillation in Long QT Syndrome by Genotype.
    Platonov PG, McNitt S, Polonsky B, Rosero SZ, Zareba W.
    Circ Arrhythm Electrophysiol; 2019 Oct 02; 12(10):e007213. PubMed ID: 31610692
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  • 13. 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 02; 20(6):475-6. PubMed ID: 12442276
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  • 16. Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
    Tester DJ, Will ML, Haglund CM, Ackerman MJ.
    Heart Rhythm; 2005 May 02; 2(5):507-17. PubMed ID: 15840476
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  • 19. Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter study.
    Itoh H, Shimizu W, Hayashi K, Yamagata K, Sakaguchi T, Ohno S, Makiyama T, Akao M, Ai T, Noda T, Miyazaki A, Miyamoto Y, Yamagishi M, Kamakura S, Horie M.
    Heart Rhythm; 2010 Oct 02; 7(10):1411-8. PubMed ID: 20541041
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