Long-QT Syndrome: From Genetics to ManagementSCHWARTZ, Peter J; CROTTI, Lia; INSOLIA, Roberto et al.Circulation. Arrhythmia and electrophysiology. 2012, Vol 5, Num 4, pp 868-877, issn 1941-3149, 10 p.Article

Postmortem long QT syndrome genetic testing for sudden unexplained death in the young. CommentaryTESTER, David J; ACKERMAN, Michael J; SCHWARTZ, Peter J et al.Journal of the American College of Cardiology. 2007, Vol 49, Num 2, pp 240-249, issn 0735-1097, 10 p.Article

Calmodulin Mutations Associated With Recurrent Cardiac Arrest in InfantsCROTTI, Lia; JOHNSON, Christopher N; PEDRAZZINI, Matteo et al.Circulation (New York, N.Y.). 2013, Vol 127, Num 9, pp 1009-1017, issn 0009-7322, 9 p.Article

Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2: Higher Recurrence of Events Under MetoprololCHOCKALINGAM, Priya; CROTTI, Lia; RYDBERG, Annika et al.Journal of the American College of Cardiology. 2012, Vol 60, Num 20, pp 2092-2099, issn 0735-1097, 8 p.Article

Spectrum and Prevalence of Mutations Involving BrS1- Through BrS12-Susceptibility Genes in a Cohort of Unrelated Patients Referred for Brugada Syndrome Genetic Testing: Implications for Genetic TestingCROTTI, Lia; MARCOU, Cherisse A; SCHWARTZ, Peter J et al.Journal of the American College of Cardiology. 2012, Vol 60, Num 15, pp 1410-1418, issn 0735-1097, 9 p.Article

Left Cardiac Sympathetic Denervation for Catecholaminergic Polymorphic Ventricular TachycardiaWILDE, Arthur A. M; BHUIYAN, Zahurul A; CROTTI, Lia et al.The New England journal of medicine. 2008, Vol 358, Num 19, pp 2024-2029, issn 0028-4793, 6 p.Article

Does pregnancy increase cardiac risk for LQT1 patients with the KCNQ1-A341V mutation?HERADIEN, Marshall J; GOOSEN, Althea; CROTTI, Lia et al.Journal of the American College of Cardiology. 2006, Vol 48, Num 7, pp 1410-1415, issn 0735-1097, 6 p.Article

Who Are the Long-QT Syndrome Patients Who Receive an Implantable Cardioverter-Defibrillator and What Happens to Them?: Data From the European Long-QT Syndrome Implantable Cardioverter-Defibrillator (LQTS ICD) RegistrySCHWARTZ, Peter J; SPAZZOLINI, Carla; TOIVONEN, Lauri et al.Circulation (New York, N.Y.). 2010, Vol 122, Num 13, pp 1272-1282, issn 0009-7322, 11 p.Article

Clinical Implications for Patients With Long QT Syndrome Who Experience a Cardiac Event During Infancy : HEART RHYTHM DISORDERSSPAZZOLINI, Carla; MULLALLY, Jamie; ROBINSON, Jennifer L et al.Journal of the American College of Cardiology. 2009, Vol 54, Num 9, pp 832-837, issn 0735-1097, 6 p.Article

NOS1AP Is a Genetic Modifier of the Long-QT SyndromeCROTTI, Lia; MONTI, Maria Cristina; INSOLIA, Roberto et al.Circulation (New York, N.Y.). 2009, Vol 120, Num 17, pp 1657-1663, issn 0009-7322, 7 p.Article

Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder populationBRINK, Paul A; CROTTI, Lia; SPAZZOLINI, Carla et al.Circulation (New York, N.Y.). 2005, Vol 112, Num 17, pp 2602-2610, issn 0009-7322, 9 p., SUPConference Paper

Long QT Syndrome―Associated Mutations in Intrauterine Fetal DeathCROTTI, Lia; TESTER, David J; GHIDONI, Alice et al.JAMA, the journal of the American Medical Association. 2013, Vol 309, Num 14, pp 1473-1482, issn 0098-7484, 10 p.Article

Vagal Reflexes Following an Exercise Stress Test: A Simple Clinical Tool for Gene-Specific Risk Stratification in the Long QT SyndromeCROTTI, Lia; SPAZZOLINI, Carla; GOOSEN, Althea et al.Journal of the American College of Cardiology. 2012, Vol 60, Num 24, pp 2515-2524, issn 0735-1097, 10 p.Article

Neural Control of Heart Rate Is an Arrhythmia Risk Modifier in Long QT Syndrome. CommentarySCHWARTZ, Peter J; VANOLI, Emilio; LA ROVERE, Maria Teresa et al.Journal of the American College of Cardiology. 2008, Vol 51, Num 9, pp 920-932, issn 0735-1097, 13 p.Article

KCNH2-K897T is a genetic modifier of latent congenital long-QT syndromeCROTTI, Lia; LUNDQUIST, Andrew L; SCHWARTZ, Peter J et al.Circulation (New York, N.Y.). 2005, Vol 112, Num 9, pp 1251-1258, issn 0009-7322, 8 p.Article

Prevalence of the Congenital Long-QT SyndromeSCHWARTZ, Peter J; STRAMBA-BADIALE, Marco; MOSCA, Fabio et al.Circulation (New York, N.Y.). 2009, Vol 120, Num 18, pp 1761-1767, issn 0009-7322, 7 p.Article

Prevalence of long-QT syndrome gene variants in sudden infant death syndromeARNESTAD, Marianne; CROTTI, Lia; SCHWARTZ, Peter J et al.Circulation (New York, N.Y.). 2007, Vol 115, Num 3, pp 361-367, issn 0009-7322, 7 p.Article

The Common Long-QT Syndrome Mutation KCNQ1/A341V Causes Unusually Severe Clinical Manifestations in Patients With Different Ethnic Backgrounds : Toward a Mutation-Specific Risk StratificationCROTTI, Lia; SPAZZOLINI, Caria; WILDE, Arthur A. M et al.Circulation (New York, N.Y.). 2007, Vol 116, Num 21, pp 2366-2375, issn 0009-7322, 10 p.Article

The jervell and lange-nielsen syndrome : Natural history, molecular basis, and clinical outcomeSCHWARTZ, Peter J; SPAZZOLINI, Carla; HORIE, Minoru et al.Circulation (New York, N.Y.). 2006, Vol 113, Num 6, pp 783-790, issn 0009-7322, 8 p.Article

A Novel Disease Gene for Brugada Syndrome: Sarcolemmal Membrane―Associated Protein Gene Mutations Impair Intracellular Trafficking of hNav1.5ISHIKAWA, Taisuke; SATO, Akinori; HIRAOKA, Masayasu et al.Circulation. Arrhythmia and electrophysiology. 2012, Vol 5, Num 6, pp 1098-1107, issn 1941-3149, 10 p.Article

Mutation-Specific Risk in Two Genetic Forms of Type 3 Long QT SyndromeLIU, Judy F; MOSS, Arthur J; MING QI et al.The American journal of cardiology. 2010, Vol 105, Num 2, pp 210-213, issn 0002-9149, 4 p.Article

High Efficacy of β-Blockers in Long-QT Syndrome Type 1 Contribution of Noncompliance and QT-Prolonging Drugs to the Occurrence of β-Blocker Treatment FailuresVINCENT, G. Michael; SCHWARTZ, Peter J; PRIORI, Silvia G et al.Circulation (New York, N.Y.). 2009, Vol 119, Num 2, pp 215-221, issn 0009-7322, 7 p.Article

Cardiac sodium channel dysfunction in sudden infant death syndromeWANG, Dao W; DESAI, Reshma R; GEORGE, Alfred L et al.Circulation (New York, N.Y.). 2007, Vol 115, Num 3, pp 368-376, issn 0009-7322, 9 p.Article

Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 familiesPRIORI, Silvia G; NAPOLITANO, Carlo; CROTTI, Lia et al.Circulation (New York, N.Y.). 2000, Vol 102, Num 20, pp 2509-2515, issn 0009-7322Article