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544 results

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Page 1
Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.
Schwartz PJ, Priori SG, Locati EH, Napolitano C, Cantù F, Towbin JA, Keating MT, Hammoude H, Brown AM, Chen LS, Colatsky TJ. Schwartz PJ, et al. Among authors: towbin ja. Circulation. 1995 Dec 15;92(12):3381-6. doi: 10.1161/01.cir.92.12.3381. Circulation. 1995. PMID: 8521555
Long-QT syndrome after age 40.
Goldenberg I, Moss AJ, Bradley J, Polonsky S, Peterson DR, McNitt S, Zareba W, Andrews ML, Robinson JL, Ackerman MJ, Benhorin J, Kaufman ES, Locati EH, Napolitano C, Priori SG, Qi M, Schwartz PJ, Towbin JA, Vincent GM, Zhang L. Goldenberg I, et al. Among authors: towbin ja. Circulation. 2008 Apr 29;117(17):2192-201. doi: 10.1161/CIRCULATIONAHA.107.729368. Epub 2008 Apr 21. Circulation. 2008. PMID: 18427134
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: towbin ja. Circulation. 2002 Feb 19;105(7):794-9. doi: 10.1161/hc0702.105124. Circulation. 2002. PMID: 11854117
New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.
Li H, Chen Q, Moss AJ, Robinson J, Goytia V, Perry JC, Vincent GM, Priori SG, Lehmann MH, Denfield SW, Duff D, Kaine S, Shimizu W, Schwartz PJ, Wang Q, Towbin JA. Li H, et al. Among authors: towbin ja. Circulation. 1998 Apr 7;97(13):1264-9. doi: 10.1161/01.cir.97.13.1264. Circulation. 1998. PMID: 9570196
Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome.
Moss AJ, Zareba W, Hall WJ, Schwartz PJ, Crampton RS, Benhorin J, Vincent GM, Locati EH, Priori SG, Napolitano C, Medina A, Zhang L, Robinson JL, Timothy K, Towbin JA, Andrews ML. Moss AJ, et al. Among authors: towbin ja. Circulation. 2000 Feb 15;101(6):616-23. doi: 10.1161/01.cir.101.6.616. Circulation. 2000. PMID: 10673253 Clinical Trial.
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: towbin ja. 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: towbin ja. Circulation. 2001 Jan 2;103(1):89-95. doi: 10.1161/01.cir.103.1.89. Circulation. 2001. PMID: 11136691 Clinical Trial.
544 results