Carlo Napolitano

Silvana Quaglini, Andrea Mazzanti, Stefania Rubrichi, 2015, Medical decision making : an international journal of the Society for Medical Decision Making.

Risk stratification in the long-QT syndrome.

Carlo Napolitano, Silvia G. Priori, Peter J. Schwartz, 2003, The New England journal of medicine.

Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism–epilepsy phenotype

Renzo Guerrini, Carlo Napolitano, Federico Sicca, 2014, Human molecular genetics.

Risk stratification in the long-QT syndrome.

Carlo Napolitano, Silvia G Priori, Alessandro Vicentini, 2003, The New England journal of medicine.

Polymorphisms in the NOS 1 AP Gene Modulate QT Interval Duration and Risk of Arrhythmias in the Long QT Syndrome

Riccardo Bellazzi, Isaac Subirana, Carlo Napolitano, 2022 .

Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals.

Michael J. Ackerman, Pyotr G. Platonov, Wojciech Zareba, 2011, Journal of the American College of Cardiology.

Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndrome.

Michael J Ackerman, Li Zhang, Wojciech Zareba, 2006, JAMA.

Induced pluripotent stem cell-derived cardiomyocytes in studies of inherited arrhythmias.

Carlo Napolitano, Silvia G Priori, S. Priori, 2013, The Journal of clinical investigation.

How Really Rare Are Rare Diseases?:

Carlo Napolitano, Silvia G Priori, S. Priori, 2003, Journal of cardiovascular electrophysiology.

Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes.

Carlo Napolitano, Silvia G Priori, Vann Bennett, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Increased Ca2+ Sensitivity of the Ryanodine Receptor Mutant RyR2R4496C Underlies Catecholaminergic Polymorphic Ventricular Tachycardia

Carlo Napolitano, Silvia G. Priori, Sylvain Richard, 2009, Circulation research.

Arrhythmogenic Mechanisms in a Mouse Model of Catecholaminergic Polymorphic Ventricular Tachycardia

José Jalife, Omer Berenfeld, Elena G Tolkacheva, 2007, Circulation research.

Epinephrine unmasks latent mutation carriers with LQT1 form of congenital long-QT syndrome.

Kenji Sunagawa, Wataru Shimizu, Carlo Napolitano, 2003, Journal of the American College of Cardiology.

Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.

Li Zhang, Wojciech Zareba, Derick R. Peterson, 2003, Journal of the American College of Cardiology.

Clinical and research data integration: the i2b2-FSM experience.

Riccardo Bellazzi, Arianna Dagliati, Valentina Tibollo, 2013, AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science.