C. Napolitano

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

Novel Arrhythmogenic Mechanism Revealed by a Long-QT Syndrome Mutation in the Cardiac Na+ Channel

S. Priori, M. Memmi, C. Napolitano, 2001, Circulation research.

Arrhythmogenesis in catecholaminergic polymorphic ventricular tachycardia: insights from a RyR2 R4496C knock-in mouse model.

Sara Negri, Marcello Imbriani, Carlo Napolitano, 2006, Circulation research.

Bridging the Dimensions of Research on Cardiac Ryanodine Receptor Mutations

C. Napolitano, 2013, Journal of cardiovascular electrophysiology.

Viral Gene Transfer Rescues Arrhythmogenic Phenotype and Ultrastructural Abnormalities in Adult Calsequestrin-Null Mice With Inherited Arrhythmias

S. Priori, C. Napolitano, S. Boncompagni, 2012, Circulation research.

Short Communication: Flecainide Exerts an Antiarrhythmic Effect in a Mouse Model of Catecholaminergic Polymorphic Ventricular Tachycardia by Increasing the Threshold for Triggered Activity

S. Priori, C. Napolitano, W. Coetzee, 2011, Circulation research.

Bidirectional Ventricular Tachycardia and Fibrillation Elicited in a Knock-In Mouse Model Carrier of a Mutation in the Cardiac Ryanodine Receptor

S. Priori, C. Napolitano, M. R. di Barletta, 2005, Circulation research.

Risk stratification in the long-QT syndrome.

S. Priori, P. Schwartz, R. Bloise, 2003, The New England journal of medicine.

Genetic testing for long QT syndrome.

S. Priori, P. Schwartz, R. Bloise, 2008, Technology Evaluation Center Assessment Program. Executive summary.

Y1767C, a novel SCN5A mutation, induces a persistent Na+ current and potentiates ranolazine inhibition of Nav1.5 channels.

S. Priori, C. Napolitano, M. Chahine, 2011, American journal of physiology. Heart and circulatory physiology.

Genetics and Arrhythmias: Diagnostic and Prognostic Applications

S. Priori, N. Monteforte, C. Napolitano, 2012 .

Genetics and arrhythmias: diagnostic and prognostic applications.

S. Priori, N. Monteforte, C. Napolitano, 2012, Revista espanola de cardiologia.

Significance of QT dispersion in the long QT syndrome.

S. Priori, P. Schwartz, C. Napolitano, 2000, Progress in cardiovascular diseases.

Genetic testing for inherited cardiac arrhythmias.

S. Priori, C. Napolitano, M. Cerrone, 2010, Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese.

When is genetic testing useful in patients suspected to have inherited cardiac arrhythmias?

S. Priori, C. Napolitano, S. Fowler, 2010, Current opinion in cardiology.

Cardiac Magnetic Resonance in Stable Coronary Artery Disease: Added Prognostic Value to Conventional Risk Profiling

S. Priori, C. Napolitano, N. Ntusi, 2018, BioMed research international.

Genetic Mechanisms of Arrhythmia

S. Priori, C. Napolitano, C. Macrae, 2012 .

Molecular underpinning of "good luck".

S. Priori, C. Napolitano, 2006, Circulation.

Arrhythmogenic Right Ventricular Cardiomyopathy: Clinical Course and Predictors of Arrhythmic Risk.

R. Bellazzi, S. Priori, A. Mazzanti, 2016, Journal of the American College of Cardiology.

Meandering pathway leading from genotyping to personalized management of long-QT syndrome.

S. Priori, C. Napolitano, 2012, Circulation.

Risk Stratification in Brugada Syndrome

M. Colombo, C. Napolitano, G. Mascioli, 2011 .

Diagnosis and treatment of catecholaminergic polymorphic ventricular tachycardia.

S. Priori, C. Napolitano, 2007, Heart rhythm.

Clinical Implications for Affected Parents and Siblings of Probands With Long-QT Syndrome

S. Priori, A. Moss, P. Schwartz, 2001, Circulation.

A Newly Characterized SCN5A Mutation Underlying Brugada Syndrome Unmasked by Hyperthermia

S. Priori, C. Napolitano, N. Mok, 2003, Journal of cardiovascular electrophysiology.

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.

Sudden Cardiac Death Sudden Cardiac Death and Genetic Ion Channelopathies Long QT , Brugada , Short QT , Catecholaminergic Polymorphic Ventricular Tachycardia , and Idiopathic Ventricular Fibrillation

S. Priori, N. Monteforte, R. Bloise, 2012 .

Sudden cardiac death and genetic ion channelopathies: long QT, Brugada, short QT, catecholaminergic polymorphic ventricular tachycardia, and idiopathic ventricular fibrillation.

S. Priori, N. Monteforte, R. Bloise, 2012, Circulation.

Gating Properties of SCN5A Mutations and the Response to Mexiletine in Long-QT Syndrome Type 3 Patients

S. Priori, R. Bloise, C. Napolitano, 2007, Circulation.

The heritable nature of the electrocardiogram: How far can population genetics go?

C. Napolitano, 2009, Heart rhythm.

Brugada syndrome and sudden cardiac death in children

S. Priori, M. Memmi, C. Napolitano, 2000, The Lancet.

Running title: Genome-wide association study in long QT syndrome

T. Werge, P. Ellinor, S. Priori, 2020 .

From catheters to vectors: the dawn of molecular electrophysiology

S. Priori, C. Napolitano, 2000, Nature Medicine.

FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death

S. Priori, J. D’Armiento, M. Memmi, 2003, Cell.

Chapter 25 – Genetics of Inherited Arrhythmias

S. Priori, C. Napolitano, 2007 .

Chapter 68 – Catecholaminergic Polymorphic Ventricular Tachycardia and Short-coupled Torsades de Pointes

S. Priori, C. Napolitano, 2004 .

Inherited Arrhythmia Syndromes: Applying the Molecular Biology and Genetic to the Clinical Management

S. Priori, C. Napolitano, A. Vicentini, 2003, Journal of Interventional Cardiac Electrophysiology.

Molecular diagnosis in a child with sudden infant death syndrome

G. Breithardt, S. Priori, P. Schwartz, 2001, The Lancet.

Early afterdepolarizations induced in vivo by reperfusion of ischemic myocardium. A possible mechanism for reperfusion arrhythmias.

S. Priori, P. Schwartz, C. Napolitano, 1990, Circulation.

Cardiac receptor activation and arrhythmogenesis.

S. Priori, P. Schwartz, C. Napolitano, 1993, European heart journal.

Electrophysiologic mechanisms involved in the development of torsades de pointes

S. Priori, P. Schwartz, C. Napolitano, 1991, Cardiovascular Drugs and Therapy.

Heart, brain, and the risk of sudden death.

C. Napolitano, 2013, Heart rhythm.

International Triadin Knockout Syndrome Registry: The Clinical Phenotype and Treatment Outcomes of Patients With Triadin Knockout Syndrome

S. Priori, P. Schwartz, C. Napolitano, 2019, Circulation. Genomic and precision medicine.

Gender differences in patients with Brugada syndrome and arrhythmic events: Data from a survey on arrhythmic events in 678 patients.

S. Priori, E. Behr, C. Napolitano, 2018, Heart rhythm.

Concealed arrhythmogenic syndromes: the hidden substrate of idiopathic ventricular fibrillation?

C. Napolitano, M. Grillo, S. Priori, 2001, Cardiovascular research.

High Efficacy of (cid:1) -Blockers in Long-QT Syndrome Type 1 Contribution of Noncompliance and QT-Prolonging Drugs to the Occurrence of (cid:1) -Blocker Treatment “Failures”

S. Priori, P. Schwartz, C. Napolitano, 2009 .

Clinical profile and genetic basis of Brugada syndrome in the Chinese population.

S. Priori, R. Bloise, C. Napolitano, 2004, Hong Kong medical journal = Xianggang yi xue za zhi.

[Brugada's syndrome: epidemiology, risk stratification, and clinical management].

S. Priori, R. Bloise, C. Napolitano, 2002, Italian heart journal. Supplement : official journal of the Italian Federation of Cardiology.

Profile of patients with Brugada syndrome presenting with their first documented arrhythmic event: Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS).

S. Priori, E. Behr, C. Napolitano, 2018, Heart rhythm.

Profile of Brugada Syndrome Patients Presenting with Their First Documented Arrhythmic Event. Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)

Zhengrong, E. Behr, C. Napolitano, 2018 .

Age KnockIn Mice Affected by Catecholaminergic Polymorphic Ventricular Tachycardia Is Gene to CASQ 2 Single Delivery of an Adeno-Associated Viral Construct to Transfer the Print

S. Priori, A. Curcio, C. Napolitano, 2014 .

Genetics of Long QT, Brugada, and Other Channelopathies

S. Priori, C. Napolitano, I. Rivolta, 2004 .

Transgenic models in cardiac arrhythmias: how close can we get to the bedside?

C. Napolitano, 2004, Cardiovascular research.

Genetic Defects of Cardiac Ion Channels. The Hidden Substrate for Torsades de Pointes

S. Priori, C. Napolitano, 2002, Cardiovascular Drugs and Therapy.

Romano-Ward and Other Congenital Long QT Syndromes

S. Priori, R. Bloise, C. Napolitano, 2004, Cardiovascular Drugs and Therapy.

Location of Mutation in the KCNQ1 and Phenotypic Presentation of Long QT Syndrome

E. Kaufman, S. Priori, A. Moss, 2003, Journal of cardiovascular electrophysiology.

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

S. Priori, K. Sunagawa, J. Towbin, 2003, Journal of the American College of Cardiology.

MINI-SYMPOSIUM: LONG QT SYNDROME AND TORSADE DE POINTES— IS THE DOCTOR OR THE PATIENT AT FAULT? Genetic Defects of Cardiac Ion Channels. The Hidden Substrate for Torsades de Pointes

S. Priori, C. Napolitano, 2002 .

Will the Spectrum of Ion Channel Diseases Increase Further in the Near Future

C. Napolitano, S. Priori, 2002 .

Genetic and molecular basis of arrhythmias

C. Napolitano, S. Priori, 2000 .

Y1767C, a novel SCN5A mutation, induces a persistent Na+ current and potentiates ranolazine inhibition of Nav1.5 channels.

S. Priori, C. Napolitano, M. Chahine, 2011, American journal of physiology. Heart and circulatory physiology.

Genetics of ventricular tachycardia

S. Priori, C. Napolitano, 2002, Current opinion in cardiology.

Genotype-Phenotype Correlation in the Long-QT Syndrome

G. Breithardt, S. Priori, A. Moss, 2001 .

Molecular Biology of the Long QT Syndrome: Impact on Management

S. Priori, P. Schwartz, C. Napolitano, 1997, Pacing and clinical electrophysiology : PACE.

Reply: Did Mutation Type Affect the Efficacy of Mexiletine Observed in Patients With LQTS Type 3?

S. Priori, A. Mazzanti, C. Napolitano, 2017, Journal of the American College of Cardiology.

The Slow Pace of the Heart and the Objectives of Molecular Cardiology

C. Napolitano, 2010, Journal of cardiovascular electrophysiology.

The Meandering Pathway Leading from Genotyping to Personalized Management of LQTS Running title: Priori et al.; Genotype-phenotype correlation in LQTS

S. Priori, C. Napolitano, 2012 .

Unusual retrospective prenatal findings in a male newborn with Timothy syndrome type 1.

S. Priori, R. Bloise, C. Napolitano, 2015, European journal of medical genetics.

56 – Gene Therapy to Treat Cardiac Arrhythmias

S. Priori, C. Napolitano, M. Denegri, 2018 .

Overexpression of CaMKII (cid:1) c in RyR2 R4496C (cid:2) / (cid:3) Knock-In Mice Leads to Altered Intracellular Ca 2 (cid:2) Handling and Increased Mortality

S. Priori, C. Napolitano, B. Pieske, 2011 .

Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator: data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS).

S. Priori, E. Behr, C. Napolitano, 2019, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Age of First Arrhythmic Event in Brugada Syndrome: Data From the SABRUS (Survey on Arrhythmic Events in Brugada Syndrome) in 678 Patients

S. Priori, E. Behr, C. Napolitano, 2017, Circulation. Arrhythmia and electrophysiology.

Natural History and Risk Stratification in Andersen-Tawil Syndrome Type 1.

S. Priori, A. Mazzanti, N. Monteforte, 2020, Journal of the American College of Cardiology.

The Contradictory Genetics of Atrial Fibrillation: The Growing Gap Between Knowledge and Clinical Implications

C. Napolitano, 2013, Journal of cardiovascular electrophysiology.

Adeno-associated virus-mediated CASQ2 delivery rescues phenotypic alterations in a patient-specific model of recessive catecholaminergic polymorphic ventricular tachycardia

S. Priori, G. Condorelli, C. Napolitano, 2016, Cell Death and Disease.

Variable phenotype of long QT syndrome patients with the same genetic defect

S. Priori, P. Schwartz, J. Towbin, 1998 .

Clinical utility gene card for: Catecholaminergic polymorphic ventricular tachycardia (CPVT)

S. Priori, M. Memmi, R. Bloise, 2013, European Journal of Human Genetics.

Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.

S. Priori, A. Moss, P. Schwartz, 1999, Circulation.

Outcomes of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Treated With β-Blockers.

S. Priori, A. Mazzanti, N. Monteforte, 2022, JAMA cardiology.

Flecainide monotherapy for catecholaminergic polymorphic ventricular tachycardia: Perspectives and limitations.

C. Napolitano, 2016, Heart rhythm.

Markovian model for wild-type and mutant (Y1795C and Y1795H) human cardiac Na/sup +/ channel

S. Severi, S. Vecchietti, S. Cavalcanti, 2003, Computers in Cardiology, 2003.

Markovian Model for Wild-Type and Mutant ( Y 1795 C and Y 1795 H ) Human Cardiac Na + Channel

S. Severi, S. Vecchietti, S. Cavalcanti, 2003 .

Catecholaminergic Polymorphic Ventricular Tachycardia: Another Inherited Arrhythmia?

C. Napolitano, S. Priori, 2002 .

Unexpected Risk Profile of a Large Pediatric Population With Brugada Syndrome.

S. Priori, A. Mazzanti, N. Monteforte, 2019, Journal of the American College of Cardiology.

Tyrosine kinase inhibitors and QTc intervals: A class effect.

S. Sleijfer, C. Napolitano, A. Malovini, 2014 .

Age of First Arrhythmic Event in Brugada Syndrome: Data from the Survey on Arrhythmic Events in Brugada Syndrome (SABRUS) in 678 Patients Age of First Arrhythmic Event in Brugada Syndrome

E. Behr, C. Napolitano, J. Brugada, 2020 .

Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation.

S. Priori, M. Memmi, C. Napolitano, 2002, The Journal of clinical investigation.

Left Cardiac Sympathetic Denervation in the Management of High-Risk Patients Affected by the Long-QT Syndrome

S. Priori, A. Moss, P. Schwartz, 2004, Circulation.

Pathogenesis and Therapy of the Idiopathic Long QT Syndrome

P. Schwartz, C. Napolitano, E. Locati, 1992, Annals of the New York Academy of Sciences.

Principal component analysis identifies abnormal complexity of repolarization in post myocardial infarction patients

S. Priori, C. Napolitano, D. Mortara, 1996 .

Natural history and genetic aspects of the Jervell and Lange-Nielsen syndrome.

Toshihiro Tanaka, S. Priori, M. Bitner-Glindzicz, 2001 .

Programmed Electrical Stimulation in Brugada Syndrome: How Reproducible Are the Results?

S. Priori, R. Bloise, C. Napolitano, 2002, Journal of cardiovascular electrophysiology.

Long QT syndrome and pregnancy.

E. Kaufman, S. Priori, A. Moss, 2007, Journal of the American College of Cardiology.

Magnetocardiographic findings and follow-up in an asymptomatic Brugada patient. Effects of Flecainide and of exercise tests

S. Priori, C. Napolitano, R. Fenici, 2007 .

Cardiac Histological Substrate in Patients With Clinical Phenotype of Brugada Syndrome

S. Priori, M. Russo, C. Napolitano, 2005, Circulation.

Role of Genetic Analyses in Cardiology: Part I: Mendelian Diseases: Cardiac Channelopathies

S. Priori, C. Napolitano, 2006, Circulation.

Monday, 27 August 2012

V. V. Ivanenko, E. A. Medvedeva, Michail I. Papafaklis, 2012 .

Association of long QT syndrome loci and cardiac events among patients treated with beta-blockers.

S. Priori, P. Schwartz, R. Bloise, 2004, JAMA.

The Elusive Link Between LQT3 and Brugada Syndrome: The Role of Flecainide Challenge

S. Priori, P. Schwartz, R. Bloise, 2000, Circulation.

S. Priori, A. Moss, P. Schwartz, 1998, Circulation.

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.

Mechanisms of Actions of Inhaled Anesthetics

P. Ellinor, S. Priori, P. Schwartz, 2003 .

R Engine Cell: integrating R into the i2b2 software infrastructure

Riccardo Bellazzi, Cristiana Larizza, Valentina Tibollo, 2011, J. Am. Medical Informatics Assoc..

95 – Timothy Syndrome

S. Priori, C. Napolitano, 2014 .

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

R. Redon, K. Strauch, P. Lambiase, 2022, Nature Genetics.

CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardia

M Miragoli, S. Priori, G. Condorelli, 2013, Cell Death and Disease.

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases

E. Ashley, A. Bollmann, E. Kaufman, 2022, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

R. Redon, P. Lambiase, P. Ellinor, 2020, Genetics in medicine : official journal of the American College of Medical Genetics.

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

T. Werge, P. Ellinor, S. Priori, 2020, Circulation.

Female predominance and transmission distortion in the long-QT syndrome.

S. Priori, M. Imboden, C. Napolitano, 2006, The New England journal of medicine.

Evaluation of the spatial aspects of T-wave complexity in the long-QT syndrome.

S. Priori, P. Schwartz, C. Napolitano, 1997, Circulation.

Venice Chart International Consensus Document on Atrial Fibrillation Ablation

G. Hindricks, H. Calkins, S. Themistoclakis, 2007, Journal of cardiovascular electrophysiology.

[Risk stratification in Brugada syndrome].

S. Priori, M. Colombo, C. Napolitano, 2011, Giornale italiano di cardiologia.

Clinical and Genetic Heterogeneity of Right Bundle Branch Block and ST-Segment Elevation Syndrome: A Prospective Evaluation of 52 Families

S. Priori, P. Schwartz, R. Bloise, 2000, Circulation.

Clinical Presentation and Outcome of Brugada Syndrome Diagnosed With the New 2013 Criteria

S. Priori, A. Mazzanti, N. Monteforte, 2016, Journal of cardiovascular electrophysiology.

Flecainide and antiarrhythmic effects in a mouse model of catecholaminergic polymorphic ventricular tachycardia.

S. Priori, C. Napolitano, Nian Liu, 2012, Trends in cardiovascular medicine.

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.

Missense Mutations in Plakophilin-2 Cause Sodium Current Deficit and Associate With a Brugada Syndrome Phenotype

S. Priori, V. Novelli, C. Napolitano, 2014, Circulation.

Magnetic resonance investigations in Brugada syndrome reveal unexpectedly high rate of structural abnormalities.

S. Priori, N. Monteforte, R. Bloise, 2009, European Heart Journal.

Interplay Between Genetic Substrate, QTc Duration, and Arrhythmia Risk in Patients With Long QT Syndrome.

R. Bellazzi, S. Priori, A. Mazzanti, 2018, Journal of the American College of Cardiology.

Genetic modulators of the phenotype in the long QT syndrome: state of the art and clinical impact.

S. Priori, M. D. Francis, V. Novelli, 2015, Current opinion in genetics & development.

Sodium Current Disorders Geneticist's View

S. Priori, S. O’Rourke, C. Napolitano, 2014 .

Genetic Testing of Inherited Arrhythmias

C. Napolitano, 2012, Pediatric Cardiology.

Genetics for the Electrophysiologist: Take Home Messages for the Clinician.

C. Napolitano, S. Cummings, 2010, Cardiac electrophysiology clinics.

Polymorphisms in the NOS1AP gene modulate QT interval duration and risk of arrhythmias in the long QT syndrome.

R. Bellazzi, A. Chakravarti, S. Priori, 2010, Journal of the American College of Cardiology.

Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

S. Priori, P. Schwartz, R. Bloise, 2005, JAMA.

Natural History of Brugada Syndrome: Insights for Risk Stratification and Management

S. Priori, R. Bloise, C. Napolitano, 2002, Circulation.

Identification of a SCN5A Founder Mutation Causing Sudden Death, Brugada Syndrome and Conduction Blocks in Southern Italy.

R. Bellazzi, A. Mazzanti, M. Memmi, 2021, Heart rhythm.

Clinical and Molecular Characterization of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

Carlo Napolitano, Silvia G. Priori, S. Priori, 2002, Circulation.

Long QT syndrome in adults.

Andrew J. Sauer, E. Kaufman, S. Priori, 2007, Journal of the American College of Cardiology.

Role of calmodulin kinase in catecholaminergic polymorphic ventricular tachycardia.

S. Priori, C. Napolitano, Nian Liu, 2011, Heart rhythm.

Genetic risk stratification in cardiac arrhythmias

S. Priori, A. Mazzanti, C. Napolitano, 2018, Current opinion in cardiology.

Gene-Specific Therapy With Mexiletine Reduces Arrhythmic Events in Patients With Long QT Syndrome Type 3

S. Priori, A. Mazzanti, N. Monteforte, 2016, Journal of the American College of Cardiology.

The usual suspects in sudden cardiac death of the young: a focus on inherited arrhythmogenic diseases

S. Priori, A. Mazzanti, Carlotta Miceli, 2014, Expert review of cardiovascular therapy.

Genetics of ion-channel disorders

S. Priori, C. Napolitano, M. Cerrone, 2012, Current opinion in cardiology.

Sudden cardiac death and genetic ion channelopathies: long QT, Brugada, short QT, catecholaminergic polymorphic ventricular tachycardia, and idiopathic ventricular fibrillation.

S. Priori, N. Monteforte, R. Bloise, 2012, Circulation.

Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Voltage–Dependent L-Type Calcium Channel

C. Napolitano, C. Antzelevitch, Charles Antzelevitch, 2011, Circulation research.

Risk factors for recurrent syncope and subsequent fatal or near-fatal events in children and adolescents with long QT syndrome.

Derick R. Peterson, E. Kaufman, S. Priori, 2011, Journal of the American College of Cardiology.

Trafficking Defects and Gating Abnormalities of a Novel SCN5A Mutation Question Gene-Specific Therapy in Long QT Syndrome Type 3

S. Severi, S. Priori, C. Napolitano, 2010, Circulation research.

Clinical implications for patients with long QT syndrome who experience a cardiac event during infancy.

E. Kaufman, S. Priori, A. Moss, 2009, Journal of the American College of Cardiology.

Yield of Genetic Screening in Inherited Cardiac Channelopathies: How to Prioritize Access to Genetic Testing

S. Priori, N. Monteforte, R. Bloise, 2009, Circulation. Arrhythmia and electrophysiology.

Therapeutic Strategies for Long-QT Syndrome: Does the Molecular Substrate Matter?

S. Priori, C. Napolitano, Nian Liu, 2008, Circulation. Arrhythmia and electrophysiology.

Risk of death in the long QT syndrome when a sibling has died.

E. Kaufman, S. Priori, A. Moss, 2008, Heart rhythm.

Risk Factors for Aborted Cardiac Arrest and Sudden Cardiac Death in Children With the Congenital Long-QT Syndrome

Derick R. Peterson, E. Kaufman, S. Priori, 2008, Circulation.

Advances in Arrhythmia and Electrophysiology Therapeutic Strategies for Long-QT Syndrome

S. Priori, C. Napolitano, Nian Liu, 2008 .

Long QT syndrome and short QT syndrome: how to make correct diagnosis and what about eligibility for sports activity

S. Priori, R. Bloise, C. Napolitano, 2006, Journal of cardiovascular medicine.

Should patients with an asymptomatic Brugada electrocardiogram undergo pharmacological and electrophysiological testing?

S. Priori, C. Napolitano, 2005, Circulation.

Association of Long QT Syndrome Loci and Cardiac Events Among Patients Treated With β-Blockers

S. Priori, P. Schwartz, R. Bloise, 2004 .

Interplay between Clinical Guidelines and Organizational Workflow Systems

Mor Peleg, Silvana Quaglini, Amnon Shabo, 2016, Methods of Information in Medicine.

β-Blockers as Antiarrhythmic Agents

S. Priori, C. Napolitano, M. Cerrone, 2006 .

Assessment of a personalized and distributed patient guidance system

et al., Yuval Shahar, Tom H. F. Broens, 2017, Int. J. Medical Informatics.

Supporting Shared Decision Making within the MobiGuide Project

Yuval Shahar, Silvia Miksch, Mor Peleg, 2013, AMIA.

International Consensus Document on Atrial Fibrillation Ablation

G. Hindricks, H. Calkins, S. Themistoclakis, 2007 .

From decision to shared-decision: Introducing patients' preferences into clinical decision analysis

Silvana Quaglini, Andrea Mazzanti, Stefania Rubrichi, 2015, Artif. Intell. Medicine.

Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia

S. Priori, G. Danieli, M. Memmi, 2001, Circulation.

Cardiac and skeletal muscle disorders caused by mutations in the intracellular Ca2+ release channels.

S. Priori, C. Napolitano, 2005, The Journal of clinical investigation.

A cardiac arrhythmia syndrome caused by loss of ankyrin-B function

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

Experimental therapy of genetic arrhythmias: disease-specific pharmacology.

S. Priori, C. Napolitano, M. Cerrone, 2006, Handbook of experimental pharmacology.

Mechanisms of I(Ks) suppression in LQT1 mutants.

S. Priori, L. Bianchi, P. Schwartz, 2000, American journal of physiology. Heart and circulatory physiology.

Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with long QT syndrome.

S. Priori, A. Moss, P. Schwartz, 2000, The American journal of cardiology.

Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome.

S. Priori, A. Moss, P. Schwartz, 1999, The American journal of cardiology.

A recessive variant of the Romano-Ward long-QT syndrome?

S. Priori, L. Bianchi, P. Schwartz, 1998, Circulation.

The genetics of cardiomyopathy: Genotyping and genetic counseling

S. Priori, C. Napolitano, S. Fowler, 2009, Current treatment options in cardiovascular medicine.

RyRCa2+ Leak Limits Cardiac Ca2+ Window Current Overcoming the Tonic Effect of Calmodulin in Mice

S. Priori, C. Napolitano, C. Delgado, 2011, PloS one.

A molecular link between the sudden infant death syndrome and the long-QT syndrome.

S. Priori, P. Schwartz, R. Bloise, 2000, The New England journal of medicine.

ESC-ERC recommendations for the use of automated external defibrillators (AEDs) in Europe.

A. Capucci, S. Priori, C. Napolitano, 2004, European heart journal.

Single Delivery of an Adeno-Associated Viral Construct to Transfer the CASQ2 Gene to Knock-In Mice Affected by Catecholaminergic Polymorphic Ventricular Tachycardia Is Able to Cure the Disease From Birth to Advanced Age

S. Priori, A. Curcio, C. Napolitano, 2014, Circulation.

Decreased RyR2 refractoriness determines myocardial synchronization of aberrant Ca2+ release in a genetic model of arrhythmia

S. Priori, C. Napolitano, S. Györke, 2013, Proceedings of the National Academy of Sciences.

In the RyR2R4496C Mouse Model of CPVT, &bgr;-Adrenergic Stimulation Induces Ca Waves by Increasing SR Ca Content and Not by Decreasing the Threshold for Ca Waves

Andrew W. Trafford, Carlo Napolitano, Silvia G. Priori, 2010, Circulation research.

Unexpected Structural and Functional Consequences of the R33Q Homozygous Mutation in Cardiac Calsequestrin: A Complex Arrhythmogenic Cascade in a Knock In Mouse Model

S. Priori, S. Bicciato, C. Napolitano, 2008, Circulation research.

MobiGuide: a personalized and patient-centric decision-support system and its evaluation in the atrial fibrillation and gestational diabetes domains

Yuval Shahar, Mor Peleg, Silvana Quaglini, 2017, User Modeling and User-Adapted Interaction.

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

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

Inherited calcium channelopathies in the pathophysiology of arrhythmias

S. Priori, C. Napolitano, M. Denegri, 2012, Nature Reviews Cardiology.

Catecholaminergic polymorphic ventricular tachycardia: A paradigm to understand mechanisms of arrhythmias associated to impaired Ca(2+) regulation.

Carlo Napolitano, Silvia G Priori, S. Priori, 2009, Heart rhythm.

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

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

Increased Ca 2 (cid:1) Sensitivity of the Ryanodine Receptor Mutant RyR2 R4496C Underlies Catecholaminergic Polymorphic Ventricular Tachycardia

S. Priori, C. Napolitano, J. Benitah, 2008 .

Molecular and Electrophysiological Bases of Catecholaminergic Polymorphic Ventricular Tachycardia

S. Priori, C. Napolitano, Uwais Mohamed, 2007, Journal of cardiovascular electrophysiology.

Clinical Phenotype and Functional Characterization of CASQ2 Mutations Associated With Catecholaminergic Polymorphic Ventricular Tachycardia

S. Priori, M. Memmi, C. Napolitano, 2006, Circulation.

Abnormal Interactions of Calsequestrin With the Ryanodine Receptor Calcium Release Channel Complex Linked to Exercise-Induced Sudden Cardiac Death

S. Priori, C. Napolitano, N. Blom, 2006, Circulation research.

Intracellular Calcium Handling Dysfunction and Arrhythmogenesis: A New Challenge for the Electrophysiologist

S. Priori, C. Napolitano, 2005, Circulation research.

Abnormal Calcium Signaling and Sudden Cardiac Death Associated With Mutation of Calsequestrin

S. Priori, C. Napolitano, D. Terentyev, 2004, Circulation research.

Identification of loss-of-function RyR2 mutations associated with idiopathic ventricular fibrillation and sudden death

S. Priori, C. Napolitano, Wenting Guo, 2021, Bioscience reports.

J-Wave Syndromes: Electrocardiographic and Clinical Aspects.

S. Priori, C. Napolitano, 2018, Cardiac electrophysiology clinics.

Programmed Ventricular Stimulation for Risk Stratification in the Brugada Syndrome: A Pooled Analysis

P. Ellinor, S. Priori, A. Mazzanti, 2016, Circulation.

Programmed Ventricular Stimulation for Risk Stratification in the Brugada Syndrome: A Pooled Analysis

P. Ellinor, S. Priori, A. Mazzanti, 2015, Circulation.

Paradoxical Effect of Increased Diastolic Ca2+ Release and Decreased Sinoatrial Node Activity in a Mouse Model of Catecholaminergic Polymorphic Ventricular Tachycardia

S. Priori, C. Napolitano, Nian Liu, 2012, Circulation.

Gene-specific therapy for inherited arrhythmogenic diseases.

S. Priori, R. Bloise, C. Napolitano, 2006, Pharmacology & therapeutics.

Cardiac ryanodine receptor calcium release deficiency syndrome

S. Priori, C. Napolitano, A. Wilde, 2021, Science Translational Medicine.

Allele-Specific Silencing of Mutant mRNA Rescues Ultrastructural and Arrhythmic Phenotype in Mice Carriers of the R4496C Mutation in the Ryanodine Receptor Gene (RYR2)

S. Priori, A. Mazzanti, C. Napolitano, 2017, Circulation research.

Subclinical abnormalities in sarcoplasmic reticulum Ca(2+) release promote eccentric myocardial remodeling and pump failure death in response to pressure overload.

S. Priori, C. Napolitano, B. Pieske, 2014, Journal of the American College of Cardiology.

The role of CACNA1C in Brugada syndrome: prevalence and phenotype of probands referred for genetic testing.

A. Mazzanti, N. Monteforte, M. Memmi, 2022, Heart rhythm.

S. Priori, E. Behr, C. Napolitano, 2018, Heart rhythm.

Challenges in Molecular Diagnostics of Channelopathies in the Next-Generation Sequencing Era: Less Is More?

M. Memmi, V. Novelli, C. Napolitano, 2016, Front. Cardiovasc. Med..

Congenital Long QT Syndrome Type 3

S. Priori, C. Napolitano, R. Bai, 2014 .

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 “Failures”

S. Priori, P. Schwartz, C. Napolitano, 2009, Circulation.

Policy statement: ESC-ERC recommendations for the use of automated external defibrillators (AEDs) in Europe.

A. Capucci, S. Priori, C. Napolitano, 2004, Resuscitation.

Peptide-Based Targeting of the L-Type Calcium Channel Corrects the Loss-of-Function Phenotype of Two Novel Mutations of the CACNA1 Gene Associated With Brugada Syndrome

S. Priori, D. Catalucci, M. Bang, 2021, Frontiers in Physiology.

Incidence and relevance of QTc-interval prolongation caused by tyrosine kinase inhibitors

S. Sleijfer, C. Napolitano, A. Malovini, 2015, British Journal of Cancer.

Rare Variation in Drug Metabolism and Long QT Genes and the Genetic Susceptibility to Acquired Long QT Syndrome

S. Priori, E. Behr, D. Roden, 2022, Circulation. Genomic and precision medicine.

Evidence for a Cardiac Ion Channel Mutation Underlying Drug‐Induced QT Prolongation and Life‐Threatening Arrhythmias

S. Priori, L. Bianchi, P. Schwartz, 2000, Journal of cardiovascular electrophysiology.

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.

53 – Inheritable Phenotypes Associated With Altered Intracellular Calcium Regulation

S. Priori, C. Napolitano, 2013 .

Calmodulin kinase II inhibition prevents arrhythmias in RyR2(R4496C+/-) mice with catecholaminergic polymorphic ventricular tachycardia.

S. Priori, C. Napolitano, W. Coetzee, 2011, Journal of molecular and cellular cardiology.

Hydroquinidine Prevents Life-Threatening Arrhythmic Events in Patients With Short QT Syndrome.

R. Bellazzi, S. Priori, A. Mazzanti, 2017, Journal of the American College of Cardiology.

Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome.

S. Priori, L. Bianchi, P. Schwartz, 1999, Human molecular genetics.

Management of untreatable ventricular arrhythmias during pharmacologic challenges with sodium channel blockers for suspected Brugada syndrome

C. Napolitano, A. Proclemer, G. Bernardi, 2018, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Flecainide Test in Brugada Syndrome: A Reproducible but Risky Tool

S. Priori, C. Napolitano, S. Simonini, 2003, Pacing and clinical electrophysiology : PACE.

Noninvasive quantification of blood potassium concentration from ECG in hemodialysis patients

Stefano Severi, Cristiana Corsi, Carlo Napolitano, 2017, Scientific Reports.

Association of Hydroxychloroquine with QTc Interval in Patients with COVID-19.

S. Priori, P. De Cata, G. Condorelli, 2020, Circulation.

Big Data as a Driver for Clinical Decision Support Systems: A Learning Health Systems Perspective

Riccardo Bellazzi, Andrea Mazzanti, Matteo Gabetta, 2018, Front. Digit. Humanit..

Differential response to Na+ channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long-QT syndrome.

S. Priori, P. Schwartz, A. Brown, 1996, Circulation research.

Supervised methods to extract clinical events from cardiology reports in Italian

Riccardo Bellazzi, Natalia Viani, Timothy A Miller, 2019, J. Biomed. Informatics.

Arrhythmogenesis in Catecholaminergic Polymorphic Ventricular Tachycardia: Insights From a RyR2 R4496C Knock-In Mouse Model

S. Priori, M. Memmi, C. Napolitano, 2006 .

Torsade de pointes. Mechanisms and management.

P. Schwartz, C. Napolitano, C Napolitano, 1994, Drugs.

Brugada syndrome

S. Priori, C. Napolitano, 2006, Orphanet journal of rare diseases.

Phenotypic characterization of Timothy syndrome - a complex cardiac and multisystem disorder

S. Priori, P. Schwartz, R. Bloise, 2005 .

Inherited arrhythmia: present and future perspectives for genetic therapy

S. Priori, C. Napolitano, 2006 .

Intracellular Calcium Handling and Inherited Arrhythmogenic Diseases

S. Priori, N. Monteforte, R. Bloise, 2011 .

Na+-dependent SR Ca2+ overload induces arrhythmogenic events in mouse cardiomyocytes with a human CPVT mutation.

S. Priori, C. Napolitano, B. Pieske, 2010, Cardiovascular research.

Overexpression of CaMKIIδc in RyR2R4496C+/- knock-in mice leads to altered intracellular Ca2+ handling and increased mortality.

S. Priori, C. Napolitano, B. Pieske, 2011, Journal of the American College of Cardiology.

Abstract 2258: Electrocardiographic Analyisis Of Arrhythmias Developing During Exercise In Patients With Catecholaminergic Polymorphic Ventricular Tachycardia: Insights For Mechanisms And Site Of Origin

S. Priori, N. Monteforte, R. Bloise, 2007 .

Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome.

P. C. Viswanathan, E. Kaufman, S. Priori, 2000, American journal of physiology. Heart and circulatory physiology.

the Electrophysiologist Intracellular Calcium Handling Dysfunction and Arrhythmogenesis : A New Challenge for

S. Priori, C. Napolitano, 2013 .

Abstract 926: Gating Properties of SCN5A Mutants Predict Response to Mexiletine in LQT3 Patients

S. Priori, M. Memmi, R. Bloise, 2006 .

Abstract 1400: Origin and Mechanisms of Ventricular Tachycardia and Fibrillation in a Knock-in Mouse Model of Catecholaminergic Polymorphic Ventricular Tachycardia

S. Priori, C. Napolitano, J. Jalife, 2006 .

Abstract 910: Catecholaminergic Polymorphic Ventricular Tachycardia: Genetics, Natural History and Response to Therapy

S. Priori, C. Napolitano, F. Drago, 2007 .

Erratum: Long QT syndrome patients with mutations on the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate: Implications for gene-specific therapy (Circulation (1995) 92 (3381-3386))

Carlo Napolitano, Peter J. Schwartz, Emanuela H. Locati, 1996 .

Sympathetic activation, ventricular repolarization and Ikr blockade: implications for the antifibrillatory efficacy of potassium channel blocking agents.

S. Priori, P. Schwartz, C. Napolitano, 1995, Journal of the American College of Cardiology.

Efficacy and Limitations of Quinidine in Patients With Brugada Syndrome

R. Bellazzi, S. Priori, A. Mazzanti, 2019, Circulation: Arrhythmia and Electrophysiology.

Genetics and Arrhythmias: Diagnostic and Prognostic Applications

S. Priori, N. Monteforte, C. Napolitano, 2012 .

How Really Rare Are Rare Diseases?:

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

Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

S. Priori, A. Moss, P. Schwartz, 1998, The New England journal of medicine.

L-type Calcium Channel Disease

S. Priori, R. Bloise, C. Napolitano, 2008 .

In silico assessment of Y1795C and Y1795H SCN5A mutations: implication for inherited arrhythmogenic syndromes.

S. Severi, S. Vecchietti, S. Cavalcanti, 2007, American journal of physiology. Heart and circulatory physiology.

Validation of a novel method for non-invasive blood potassium quantification from the ECG

S. Severi, C. Napolitano, D. Mortara, 2012, 2012 Computing in Cardiology.

Computer simulation of wild-type and mutant human cardiac Na+ current

Stefano Severi, Carlo Napolitano, Silvia G. Priori, 2006, Medical and Biological Engineering and Computing.

Use of Patient Generated Data from Social Media and Collaborative Filtering for Preferences Elicitation in Shared Decision Making

Riccardo Bellazzi, Silvana Quaglini, John H. Holmes, 2014, AAAI Fall Symposia.

Gene-Specific Therapy With Mexiletine Reduces Arrhythmic Events in Patients With Long QT Syndrome Type 3

S. Priori, A. Mazzanti, N. Monteforte, 2016, Journal of the American College of Cardiology.

Programmed Ventricular Stimulation for Risk Stratification in the Brugada Syndrome: A Pooled Analysis

P. Ellinor, S. Priori, A. Mazzanti, 2016, Circulation.

Long QT syndrome in adults.

Derick R. Peterson, Andrew J. Sauer, E. Kaufman, 2007, Journal of the American College of Cardiology.

Left Cardiac Sympathetic Denervation in the Management of High-Risk Patients Affected by the Long-QT Syndrome

S. Priori, A. Moss, P. Schwartz, 2004, Circulation.

[Long QT syndrome and Brugada syndrome: 2 aspects of the same disease?].

S. Priori, P. Schwartz, C. Napolitano, 2001, Italian heart journal. Supplement : official journal of the Italian Federation of Cardiology.

Cardiac Sodium Channel Diseases

S. Priori, C. Napolitano, I. Rivolta, 2003, Clinical chemistry and laboratory medicine.

Sudden cardiac death and genetic ion channelopathies: long QT, Brugada, short QT, catecholaminergic polymorphic ventricular tachycardia, and idiopathic ventricular fibrillation.

S. Priori, N. Monteforte, R. Bloise, 2012, Circulation.

Sudden Cardiac Death Sudden Cardiac Death and Genetic Ion Channelopathies Channelopathies Associated with Prolonged Repolarization Lqts: Definition and Pathophysiology Clinical Manifestations and Management Lqts Diagnosis Should Be Considered in All Patients Pres- Enting with Qtc Ͼ440 Milliseconds i

S. Priori, N. Monteforte, R. Bloise, 2022 .

Risk stratification in Brugada syndrome: results of the PRELUDE (PRogrammed ELectrical stimUlation preDictive valuE) registry.

S. Priori, M. Colombo, C. Napolitano, 2012, Journal of the American College of Cardiology.

Sudden cardiac death and genetic ion channelopathies: long QT, Brugada, short QT, catecholaminergic polymorphic ventricular tachycardia, and idiopathic ventricular fibrillation.

S. Priori, N. Monteforte, R. Bloise, 2012, Circulation.

Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome.

S. Priori, C. Napolitano, A. Del Bufalo, 2004, Canadian Journal of Cardiology.

Information extraction from Italian medical reports: An ontology-driven approach

Riccardo Bellazzi, Cristiana Larizza, Valentina Tibollo, 2018, Int. J. Medical Informatics.

Abstract 2257: KCNJ2 Mutations in Patients Referred for Catecholaminergic Polymorphic Ventricular Tachycardia Gene Screening

S. Priori, M. Memmi, C. Napolitano, 2007 .

Calmodulin kinase II inhibition prevents arrhythmias in RyR2(R4496C+/-) mice with catecholaminergic polymorphic ventricular tachycardia.

S. Priori, C. Napolitano, W. Coetzee, 2011, Journal of molecular and cellular cardiology.

Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome Running title: Genome-wide association study in long QT syndrome

T. Werge, P. Ellinor, S. Priori, 2020 .

R Engine Cell: integrating R into the i2b2 software infrastructure

C. Larizza, R. Bellazzi, S. Priori, 2011, J. Am. Medical Informatics Assoc..

Late gadolinium enhancement by cardiovascular magnetic resonance is complementary to left ventricle ejection fraction in predicting prognosis of patients with stable coronary artery disease

S. Priori, C. Napolitano, P. Baiardi, 2012, Journal of Cardiovascular Magnetic Resonance.

Clinical timelines development from textual medical reports in Italian

Riccardo Bellazzi, Valentina Tibollo, Natalia Viani, 2017, 2017 IEEE 3rd International Forum on Research and Technologies for Society and Industry (RTSI).

Policy statement: ESC-ERC recommendations for the use of automated external defibrillators (AEDs) in Europe.

A. Capucci, S. Priori, C. Napolitano, 2004, Resuscitation.

Patient-tailored Workflow Patterns from Clinical Practice Guidelines Recommendations

Mor Peleg, Silvana Quaglini, Pnina Soffer, 2013, MedInfo.

Catecholaminergic polymorphic ventricular tachycardia: A paradigm to understand mechanisms of arrhythmias associated to impaired Ca(2+) regulation.

S. Priori, C. Napolitano, M. Cerrone, 2009, Heart rhythm.

E. Ashley, A. Bollmann, E. Kaufman, 2022, Journal of arrhythmia.

Assessment of a personalized and distributed patient guidance system

Carlos Marcos Lagunar, Roxana Ioana Budasu, Adi Fux, 2017, Int. J. Medical Informatics.

Y1767C, a novel SCN5A mutation, induces a persistent Na (cid:1) current and potentiates ranolazine inhibition of Na v 1.5 channels

S. Priori, C. Napolitano, Hai Huang, 2010 .

Novel Insight Into the Natural History of Short QT Syndrome

S. Priori, A. Mazzanti, A. Kanthan, 2014, Journal of the American College of Cardiology.