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Page 1
Congenital short QT syndrome.
Crotti L, Taravelli E, Girardengo G, Schwartz PJ. Crotti L, et al. Among authors: schwartz pj. Indian Pacing Electrophysiol J. 2010 Feb 1;10(2):86-95. Indian Pacing Electrophysiol J. 2010. PMID: 20126594 Free PMC article.
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.
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.
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
Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.
Arnestad M, Crotti L, Rognum TO, Insolia R, Pedrazzini M, Ferrandi C, Vege A, Wang DW, Rhodes TE, George AL Jr, Schwartz PJ. Arnestad M, et al. Among authors: schwartz pj. Circulation. 2007 Jan 23;115(3):361-7. doi: 10.1161/CIRCULATIONAHA.106.658021. Epub 2007 Jan 8. Circulation. 2007. PMID: 17210839
640 results