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641 results

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Impact of clinical and genetic findings on the management of young patients with Brugada syndrome.
Andorin A, Behr ER, Denjoy I, Crotti L, Dagradi F, Jesel L, Sacher F, Petit B, Mabo P, Maltret A, Wong LC, Degand B, Bertaux G, Maury P, Dulac Y, Delasalle B, Gourraud JB, Babuty D, Blom NA, Schwartz PJ, Wilde AA, Probst V. Andorin A, et al. Among authors: schwartz pj. Heart Rhythm. 2016 Jun;13(6):1274-82. doi: 10.1016/j.hrthm.2016.02.013. Epub 2016 Feb 24. Heart Rhythm. 2016. PMID: 26921764
Molecular biology of the long QT syndrome: impact on management.
Priori SG, Napolitano C, Paganini V, Cantù F, Schwartz PJ. Priori SG, et al. Among authors: schwartz pj. Pacing Clin Electrophysiol. 1997 Aug;20(8 Pt 2):2052-7. doi: 10.1111/j.1540-8159.1997.tb03626.x. Pacing Clin Electrophysiol. 1997. PMID: 9272507 Review.
Genetic and molecular basis of cardiac arrhythmias; impact on clinical management. Study group on molecular basis of arrhythmias of the working group on arrhythmias of the european society of cardiology.
Priori SG, Barhanin J, Hauer RN, Haverkamp W, Jongsma HJ, Kleber AG, McKenna WJ, Roden DM, Rudy Y, Schwartz K, Schwartz PJ, Towbin JA, Wilde A. Priori SG, et al. Among authors: schwartz k, schwartz pj. Eur Heart J. 1999 Feb;20(3):174-95. doi: 10.1053/euhj.1998.1220. Eur Heart J. 1999. PMID: 10082151 Review. No abstract available.
Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families.
Priori SG, Napolitano C, Gasparini M, Pappone C, Della Bella P, Brignole M, Giordano U, Giovannini T, Menozzi C, Bloise R, Crotti L, Terreni L, Schwartz PJ. Priori SG, et al. Among authors: schwartz pj. Circulation. 2000 Nov 14;102(20):2509-15. doi: 10.1161/01.cir.102.20.2509. Circulation. 2000. PMID: 11076825 Clinical Trial.
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: schwartz k. Circulation. 2001 Jan 2;103(1):89-95. doi: 10.1161/01.cir.103.1.89. Circulation. 2001. PMID: 11136691 Clinical Trial.
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
Crotti L, Lundquist AL, Insolia R, Pedrazzini M, Ferrandi C, De Ferrari GM, Vicentini A, Yang P, Roden DM, George AL Jr, Schwartz PJ. Crotti L, et al. Among authors: schwartz pj. Circulation. 2005 Aug 30;112(9):1251-8. doi: 10.1161/CIRCULATIONAHA.105.549071. Epub 2005 Aug 22. Circulation. 2005. PMID: 16116052
641 results