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Page 1
Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome.
Zareba W, Moss AJ, Sheu G, Kaufman ES, Priori S, Vincent GM, Towbin JA, Benhorin J, Schwartz PJ, Napolitano C, Hall WJ, Keating MT, Qi M, Robinson J, Andrews ML; International LQTS Registry, University of Rochester, Rochester, New York. Zareba W, et al. Among authors: keating mt. J Cardiovasc Electrophysiol. 2003 Nov;14(11):1149-53. doi: 10.1046/j.1540-8167.2003.03177.x. J Cardiovasc Electrophysiol. 2003. PMID: 14678125
Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.
Moss AJ, Zareba W, Kaufman ES, Gartman E, Peterson DR, Benhorin J, Towbin JA, Keating MT, Priori SG, Schwartz PJ, Vincent GM, Robinson JL, Andrews ML, Feng C, Hall WJ, Medina A, Zhang L, Wang Z. Moss AJ, et al. Among authors: keating mt. Circulation. 2002 Feb 19;105(7):794-9. doi: 10.1161/hc0702.105124. Circulation. 2002. PMID: 11854117
Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes.
Zhang L, Timothy KW, Vincent GM, Lehmann MH, Fox J, Giuli LC, Shen J, Splawski I, Priori SG, Compton SJ, Yanowitz F, Benhorin J, Moss AJ, Schwartz PJ, Robinson JL, Wang Q, Zareba W, Keating MT, Towbin JA, Napolitano C, Medina A. Zhang L, et al. Among authors: keating mt. Circulation. 2000 Dec 5;102(23):2849-55. doi: 10.1161/01.cir.102.23.2849. Circulation. 2000. PMID: 11104743
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.
Schwartz PJ, Priori SG, Spazzolini C, Moss AJ, Vincent GM, Napolitano C, Denjoy I, Guicheney P, Breithardt G, Keating MT, Towbin JA, Beggs AH, Brink P, Wilde AA, Toivonen L, Zareba W, Robinson JL, Timothy KW, Corfield V, Wattanasirichaigoon D, Corbett C, Haverkamp W, Schulze-Bahr E, Lehmann MH, Schwartz K, Coumel P, Bloise R. Schwartz PJ, et al. Among authors: keating mt. Circulation. 2001 Jan 2;103(1):89-95. doi: 10.1161/01.cir.103.1.89. Circulation. 2001. PMID: 11136691 Clinical Trial.
Locus heterogeneity of autosomal dominant long QT syndrome.
Curran M, Atkinson D, Timothy K, Vincent GM, Moss AJ, Leppert M, Keating M. Curran M, et al. J Clin Invest. 1993 Aug;92(2):799-803. doi: 10.1172/JCI116653. J Clin Invest. 1993. PMID: 8102381 Free PMC article.
128 results