S. Castelletti

W. McKenna, S. Castelletti, A. Vischer, 2017, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

The Female Athlete’s Heart: Overview and Management of Cardiovascular Diseases

S. Castelletti, S. Gati, 2021, European cardiology.

Abnormal myocardial expression of SAP97 is associated with arrhythmogenic risk.

P. Schwartz, C. Antzelevitch, D. Tester, 2020, American journal of physiology. Heart and circulatory physiology.

Effective Study: Development and Application of a Question‐Driven, Time‐Effective Cardiac Magnetic Resonance Scanning Protocol

P. Kellman, G. Parati, L. Badano, 2021, Journal of the American Heart Association.

Clinical application of CMR in cardiomyopathies: evolving concepts and techniques

G. Pontone, C. Autore, P. Filardi, 2022, Heart Failure Reviews.

Cardiac Fabry Disease With Late Gadolinium Enhancement Is a Chronic Inflammatory Cardiomyopathy.

J. Moon, A. Mehta, S. Castelletti, 2016, Journal of the American College of Cardiology.

Cardiac screening prior to return to play after SARS-CoV-2 infection: focus on the child and adolescent athlete: A Clinical Consensus Statement of the Task Force for Childhood Health of the European Association of Preventive Cardiology

E. Verhagen, A. Biffi, J. Niebauer, 2022, European Journal of Preventive Cardiology.

Partial Pericardial Agenesis Mimicking Arrhythmogenic Right Ventricular Cardiomyopathy.

G. Parati, F. Cecchi, L. Crotti, 2019, Clinical journal of sport medicine : official journal of the Canadian Academy of Sport Medicine.

Loss of function desmoplakin I and II mutations underlie dominant arrhythmogenic diomyopathy with a hair and skin phenotype Maruthappu,

D. Kelsell, P. Syrris, K. Green, 2018 .

Electrocardiographic differentiation of idiopathic right ventricular outflow tract ectopy from early arrhythmogenic right ventricular cardiomyopathy

P. Lambiase, D. Corrado, W. McKenna, 2016, 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.

Appropriate use criteria for cardiovascular MRI: SIC - SIRM position paper Part 2 (myocarditis, pericardial disease, cardiomyopathies and valvular heart disease).

G. Pontone, C. Indolfi, G. Aquaro, 2021, Journal of cardiovascular medicine.

Epicardial myocardial strain abnormalities may identify the earliest stages of arrhythmogenic cardiomyopathy

J. Moon, P. Syrris, W. McKenna, 2016, The International Journal of Cardiovascular Imaging.

From the last EuroPrevent towards the first ESC Preventive Cardiology Congress

S. Castelletti, P. Adami, 2019, European journal of preventive cardiology.

Cardiovascular magnetic resonance in hypertrophic cardiomyopathy and infiltrative cardiomyopathy

J. Moon, R. Schofield, S. Castelletti, 2016 .

Mutation location and IKs regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region.

P. Schwartz, P. Brink, P. Volders, 2021, European heart journal.

Hypertrophic cardiomyopathy: insights from extracellular volume mapping.

P. Kellman, J. Moon, C. Manisty, 2021, European journal of preventive cardiology.

A Primary Prevention Clinical Risk Score Model for Patients With Brugada Syndrome (BRUGADA-RISK).

P. Lambiase, R. Hunter, É. Marijon, 2020, JACC. Clinical electrophysiology.

Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome

P. Schwartz, M. Pedrazzini, L. Crotti, 2020, Circulation.

From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2.

P. Schwartz, G. Parati, L. Crotti, 2019, European heart journal.

Fear of Sudden Death During Sport Activity and the Long QT Syndrome

P. Schwartz, S. Castelletti, F. Dagradi, 2021, Sport-related sudden cardiac death.

Cardiology in 280 characters.

S. Castelletti, Victoria Delgado, C. Aguiar, 2021, European heart journal.

Electrocardiographic differentiation of idiopathic right ventricular outflow tract ectopy from early arrhythmogenic right ventricular cardiomyopathy.

Mitral valve prolapse and sport: how much prolapse is too prolapsing?

S. Castelletti, 2020, European journal of preventive cardiology.

Prevalence of cardiac amyloidosis among adult patients referred to tertiary centres with an initial diagnosis of hypertrophic cardiomyopathy.

G. Parati, F. Girolami, I. Olivotto, 2020, International journal of cardiology.

Diagnostic Clues for the Diagnosis of Nonsarcomeric Hypertrophic Cardiomyopathy (Phenocopies): Amyloidosis, Fabry Disease, and Mitochondrial Disease

P. Elliott, F. Cecchi, G. Limongelli, 2018, Journal of cardiovascular echography.

The Risk of Sudden Unexpected Cardiac Death in Children: Epidemiology, Clinical Causes, and Prevention.

G. Limongelli, F. Drago, P. Calabrò, 2022, Heart failure clinics.

Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1.

P. Schwartz, E. Valente, M. Mura, 2018, Stem cell research.

Age-dependent diagnostic yield of echocardiography as a second-line diagnostic investigation in athletes with abnormalities at preparticipation screening

G. Parati, S. Bianchi, I. Olivotto, 2021, Journal of cardiovascular medicine.

To be, or not to be engaged in sport activities, that is the amletic question for patients with coronary artery disease

L. Crotti, S. Castelletti, 2020, European journal of preventive cardiology.

Advanced Arrhythmogenic Cardiomyopathy in Former Marathon Runner.

G. Parati, S. Castelletti, G. Perego, 2018, Circulation. Cardiovascular imaging.

T1 mapping in severe aortic stenosis: insights into LV remodeling

J. Moon, C. Manisty, M. Fontana, 2015, Journal of Cardiovascular Magnetic Resonance.

Monday, 27 August 2012

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

Occult Transthyretin Cardiac Amyloid in Severe Calcific Aortic Stenosis: Prevalence and Prognosis in Patients Undergoing Surgical Aortic Valve Replacement.

S. K. White, J. Moon, P. Hawkins, 2016, Circulation. Cardiovascular imaging.

Indications and utility of cardiac genetic testing in athletes.

E. Behr, A. Wilde, C. Basso, 2022, European journal of preventive cardiology.

The athlete's heart from Philippides to the modern marathon runners.

S. Castelletti, G. Pieles, 2022, European heart journal.

Automatic Measurement of the Myocardial Interstitium: Synthetic Extracellular Volume Quantification Without Hematocrit Sampling.

James C Moon, Peter Kellman, Matthew D Robson, 2016, JACC. Cardiovascular imaging.

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.

Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants

D. Roden, P. Schwartz, W. Shimizu, 2021, Circulation. Genomic and precision medicine.

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.

Moebius syndrome: clinical features, diagnosis, management and early intervention

Matteo Porro, F. Mosca, O. Picciolini, 2016, Italian Journal of Pediatrics.

Risk score for the exclusion of arrhythmic events in arrhythmogenic right ventricular cardiomyopathy at first presentation.

E. Behr, A. Krahn, P. Syrris, 2019, International journal of cardiology.

Circadian and Seasonal Pattern of Arrhythmic Events in Arrhythmogenic Cardiomyopathy Patients

P. Lambiase, M. Orini, L. Crotti, 2023, International journal of environmental research and public health.

Diagnosis and management of hypertrophic cardiomyopathy

Antonis Pantazis, S. Castelletti, A. Pantazis, 2015, Echo research and practice.

Recommendations for participation in leisure-time physical activity and competitive sports of patients with arrhythmias and potentially arrhythmogenic conditions. Part 2: ventricular arrhythmias, channelopathies, and implantable defibrillators.

H. Heidbuchel, P. Schwartz, D. Corrado, 2020, 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.

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 Testing

P. Schwartz, D. Tester, M. Ackerman, 2022 .

Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation.

P. Schwartz, G. Parati, P. Syrris, 2017, International journal of cardiology.

Occult Transthyretin Cardiac Amyloid in Severe Calcific Aortic StenosisCLINICAL PERSPECTIVE

J. Moon, P. Hawkins, M. Fontana, 2016 .

Clinical recommendations of cardiac magnetic resonance, Part I: ischemic and valvular heart disease: a position paper of the working group 'Applicazioni della Risonanza Magnetica' of the Italian Society of Cardiology.

G. Pontone, G. Aquaro, L. Ait-Ali, 2017, Journal of cardiovascular medicine.

SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families

R. Redon, E. Behr, T. Meitinger, 2020, Circulation. Genomic and precision medicine.

Specific Cardiovascular Diseases and Competitive Sports Participation: Channelopathies

L. Crotti, S. Castelletti, 2020 .

Mexiletine Shortens the QT Interval in Patients With Potassium Channel-Mediated Type 2 Long QT Syndrome.

P. Schwartz, M. Ackerman, L. Crotti, 2019, Circulation. Arrhythmia and electrophysiology.

Late gadolinium enhancement in Brugada syndrome: A marker for subtle underlying cardiomyopathy?

E. Behr, L. Anderson, J. Moon, 2017, Heart rhythm.

A comprehensive electrocardiographic, molecular, and echocardiographic study of Brugada syndrome: validation of the 2013 diagnostic criteria.

P. Schwartz, L. Crotti, S. Castelletti, 2014, Heart rhythm.

Myocardial T1 mapping.

James C Moon, Chiara Bucciarelli-Ducci, Viviana Maestrini, 2015, Circulation journal : official journal of the Japanese Circulation Society.

Clinical application of CMR in cardiomyopathies: evolving concepts and techniques

G. Pontone, C. Autore, P. Filardi, 2022, Heart Failure Reviews.

Abnormal septal convexity into the left ventricle occurs in subclinical hypertrophic cardiomyopathy

P. Elliott, J. Moon, C. Manisty, 2015, Journal of Cardiovascular Magnetic Resonance.

Left Cardiac Sympathetic Denervation for Long QT Syndrome: 50 Years' Experience Provides Guidance for Management.

P. Schwartz, L. Crotti, S. Castelletti, 2021, JACC. Clinical electrophysiology.

Electroanatomic mapping in athletes: Why and when. An expert opinion paper from the Italian society of sports cardiology.

A. Dello Russo, A. Pelliccia, V. Palmieri, 2023, International journal of cardiology.

From the phenotype to precision medicine: an update on the cardiomyopathies diagnostic workflow

C. Autore, G. Limongelli, L. Crotti, 2023, Journal of cardiovascular medicine.

EuroPrevent 2018, cardiovascular prevention at its highest levels

S. Castelletti, P. Adami, 2018, European journal of preventive cardiology.

Interpretation and management of premature ventricular beats in athletes: An expert opinion document of the Italian Society of Sports Cardiology (SICSPORT).

D. Andreini, D. Corrado, A. Dello Russo, 2023, International journal of cardiology.

Moebius syndrome: clinical features, diagnosis, management and early intervention.

Matteo Porro, F. Mosca, O. Picciolini, 2016, Italian journal of pediatrics.

Remote Monitoring of the QT Interval and Emerging Indications for Arrhythmia Prevention.

P. Schwartz, S. Castelletti, B. Winkel, 2021, Cardiac Electrophysiology Clinics.

Myocardial T1 mapping.

J. Moon, C. Manisty, S. Castelletti, 2015, Circulation journal : official journal of the Japanese Circulation Society.

The ventricular ectopic QRS interval (VEQSI): Diagnosis of arrhythmogenic right ventricular cardiomyopathy in patients with incomplete disease expression.

G. Boriani, E. Behr, G. Domenichini, 2016, Heart rhythm.

Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation.

P. Schwartz, G. Parati, P. Syrris, 2017, International journal of cardiology.

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 testing.

P. Schwartz, D. Tester, A. Medeiros-Domingo, 2012, Journal of the American College of Cardiology.

Evolution in Managing Long QT Syndrome: From Registries to Centers of Excellence.

P. Schwartz, S. Castelletti, F. Dagradi, 2017, Journal of the American College of Cardiology.

Athlete's Heart: A Cardiovascular Step-By-Step Multimodality Approach

Alessandro Serio, A. Biffi, G. Limongelli, 2023, Reviews in Cardiovascular Medicine.

Unlocking the potential of Artificial Intelligence in Sports Cardiology: does it have a role in evaluating athlete's heart?

D. Niederseer, S. Ortega-Martorell, D. Oxborough, 2024, European journal of preventive cardiology.

Systolic anterior motion of the anterior mitral valve leaflet begins in subclinical hypertrophic cardiomyopathy

J. Moon, G. Captur, P. Syrris, 2023, European heart journal. Cardiovascular Imaging.

The role of echocardiography in sports cardiology: An expert opinion statement of the Italian Society of Sports Cardiology (SIC sport).

V. Palmieri, M. Bianco, S. Castelletti, 2024, International Journal of Cardiology.