Related references
Note: Only part of the references are listed.Pre-participation sport screening Don't miss focus
Silvia Castelletti et al.
EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY (2022)
Left Cardiac Sympathetic Denervation for Long QT Syndrome 50 Years' Experience Provides Guidance for Management
Veronica Dusi et al.
JACC-CLINICAL ELECTROPHYSIOLOGY (2022)
Yield and clinical significance of genetic screening in elite and amateur athletes
Giuseppe Limongelli et al.
EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY (2021)
Symptoms Preceding Sports-Related Sudden Cardiac Death in Persons Aged 1-49 Years
Emma Ritsmer Stormholt et al.
CURRENT CARDIOLOGY REPORTS (2021)
Role of Clinical Genetic Testing in the Management of Aortopathies
Stephanie L. Harris et al.
CURRENT CARDIOLOGY REPORTS (2021)
The Female Athlete's Heart: Overview and Management of Cardiovascular Diseases
Silvia Castelletti et al.
EUROPEAN CARDIOLOGY REVIEW (2021)
Clinical and molecular characteristics of 168 probands and 65 relatives with a clinical presentation of classical Ehlers-Danlos syndrome
Marlies Colman et al.
HUMAN MUTATION (2021)
Evolving Diagnostic Criteria for Arrhythmogenic Cardiomyopathy
Domenico Corrado et al.
JOURNAL OF THE AMERICAN HEART ASSOCIATION (2021)
Marfan syndrome
Dianna M. Milewicz et al.
NATURE REVIEWS DISEASE PRIMERS (2021)
Early-Onset Atrial Fibrillation and Heritable Heart Disease-To Test or Not to Test?
Gordon F. Tomaselli et al.
JAMA CARDIOLOGY (2021)
Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes
Zachary T. Yoneda et al.
JAMA CARDIOLOGY (2021)
Noncompaction Cardiomyopathy-History and Current Knowledge for Clinical Practice
Birgit J. Gerecke et al.
JOURNAL OF CLINICAL MEDICINE (2021)
A Primary Prevention Clinical Risk Score Model for Patients With Brugada Syndrome (BRUGADA-RISK)
Shohreh Honarbakhsh et al.
JACC-CLINICAL ELECTROPHYSIOLOGY (2021)
Risk stratification in Brugada syndrome: the challenge of the grey zone
Pietro Delise
EUROPEAN HEART JOURNAL (2021)
How to evaluate premature ventricular beats in the athlete: critical review and proposal of a diagnostic algorithm
Domenico Corrado et al.
BRITISH JOURNAL OF SPORTS MEDICINE (2020)
Diagnosis of arrhythmogenic cardiomyopathy: The Padua criteria
Domenico Corrado et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY (2020)
Inherited cardiac arrhythmias
Peter J. Schwartz et al.
NATURE REVIEWS DISEASE PRIMERS (2020)
Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome
Federica Dagradi et al.
CIRCULATION (2020)
2020 AHA/ACC Guideline for the Diagnosis and Treatment of Patients With Hypertrophic Cardiomyopathy: Executive Summary A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines
Steve R. Ommen et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2020)
Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosis
Domenico Corrado et al.
EUROPEAN HEART JOURNAL (2020)
Clinical Implications of Identifying Pathogenic Variants in Individuals With Thoracic Aortic Dissection
Brooke N. Wolford et al.
CIRCULATION-GENOMIC AND PRECISION MEDICINE (2019)
International recommendations for electrocardiographic interpretation in athletes
Sanjay Sharma et al.
EUROPEAN HEART JOURNAL (2018)
Diagnostic Yield of Genetic Testing in Young Athletes With T-Wave Inversion
Nabeel Sheikh et al.
CIRCULATION (2018)
Prevalence of Pathogenic Gene Mutations and Prognosis Do Not Differ in Isolated Left Ventricular Dysfunction Compared With Dilated Cardiomyopathy
Mark R. Hazebroek et al.
CIRCULATION-HEART FAILURE (2018)
A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3
Dorien Schepers et al.
HUMAN MUTATION (2018)
Common presentation of rare cardiac diseases: Arrhythmias
Iacopo Olivotto et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY (2018)
Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy
Jaap I. van Waning et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2018)
The Diagnostic Yield of Brugada Syndrome After Sudden Death With Normal Autopsy
Michael Papadakis et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2018)
Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights From the Sarcomeric Human Cardiomyopathy Registry (SHaRe)
Carolyn Y. Ho et al.
CIRCULATION (2018)
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation
Seung Hoan Choi et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2018)
Utility of genetics for risk stratification in pediatric hypertrophic cardiomyopathy
J. Mathew et al.
CLINICAL GENETICS (2018)
A score model to predict risk of events in patients with Brugada Syndrome
Juan Sieira et al.
EUROPEAN HEART JOURNAL (2017)
Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation
Silvia Castelletti et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY (2017)
Sudden Cardiac Arrest during Participation in Competitive Sports
Cameron H. Landry et al.
NEW ENGLAND JOURNAL OF MEDICINE (2017)
A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular Noncompaction
Ce Wang et al.
JOURNAL OF THE AMERICAN HEART ASSOCIATION (2017)
Arrhythmogenic Cardiomyopathy
Domenico Corrado et al.
CIRCULATION RESEARCH (2017)
Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome A Japanese Multicenter Registry
Kenichiro Yamagata et al.
CIRCULATION (2017)
Hereditary Influence in Thoracic Aortic Aneurysm and Dissection
Eric M. Isselbacher et al.
CIRCULATION (2016)
Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases
Yigal M. Pinto et al.
EUROPEAN HEART JOURNAL (2016)
The Diagnosis and Evaluation of Dilated Cardiomyopathy
Alan G. Japp et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2016)
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies
Martin F. Ortiz-Genga et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2016)
Long-Term Arrhythmic and Nonarrhythmic Outcomes of Lamin A/C Mutation Carriers
Saurabh Kumar et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2016)
Etiology of Sudden Death in Sports Insights From a United Kingdom Regional Registry
Gherardo Finocchiaro et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2016)
Arrhythmogenic cardiomyopathy
Kalliopi Pilichou et al.
ORPHANET JOURNAL OF RARE DISEASES (2016)
Clinical Profile of Athletes With Hypertrophic Cardiomyopathy
Nabeel Sheikh et al.
CIRCULATION-CARDIOVASCULAR IMAGING (2015)
Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathy
Oyediran Akinrinade et al.
EUROPEAN HEART JOURNAL (2015)
2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC) Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC)
Silvia G. Priori et al.
EUROPEAN HEART JOURNAL (2015)
Next-generation sequencing for the diagnosis of cardiac arrhythmia syndromes
Steven A. Lubitz et al.
HEART RHYTHM (2015)
Myofibrillar instability exacerbated by acute exercise in filaminopathy
Frederic Chevessier et al.
HUMAN MOLECULAR GENETICS (2015)
The genetic basis for inherited forms of sinoatrial dysfunction and atrioventricular node dysfunction
Raffaella Milanesi et al.
JOURNAL OF INTERVENTIONAL CARDIAC ELECTROPHYSIOLOGY (2015)
Worldwide Epidemiology of Atrial Fibrillation A Global Burden of Disease 2010 Study
Sumeet S. Chugh et al.
CIRCULATION (2014)
A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM Risk-SCD)
Constantinos O'Mahony et al.
EUROPEAN HEART JOURNAL (2014)
2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy The Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC)
Perry M. Elliott et al.
EUROPEAN HEART JOURNAL (2014)
2014 ESC Guidelines on the diagnosis and treatment of aortic diseases
Raimund Erbel et al.
EUROPEAN HEART JOURNAL (2014)
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing
Trevor J. Pugh et al.
GENETICS IN MEDICINE (2014)
Adult Left Ventricular Noncompaction Reappraisal of Current Diagnostic Imaging Modalities
Sabiha Gati et al.
JACC-CARDIOVASCULAR IMAGING (2014)
Compound and Digenic Heterozygosity Predicts Lifetime Arrhythmic Outcome and Sudden Cardiac Death in Desmosomal Gene-Related Arrhythmogenic Right Ventricular Cardiomyopathy
Ilaria Rigato et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2013)
Unexplained sudden death, focussing on genetics and family phenotyping
Hariharan Raju et al.
CURRENT OPINION IN CARDIOLOGY (2013)
The long QT syndrome: a transatlantic clinical approach to diagnosis and therapy
Peter J. Schwartz et al.
EUROPEAN HEART JOURNAL (2013)
Increased left ventricular trabeculation in highly trained athletes: do we need more stringent criteria for the diagnosis of left ventricular non-compaction in athletes?
Sabiha Gati et al.
HEART (2013)
Prognostic significance of early repolarization in inferolateral leads in Brugada patients with documented ventricular fibrillation: A novel risk factor for Brugada syndrome with ventricular fibrillation
Hiro Kawata et al.
HEART RHYTHM (2013)
HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes
Silvia G. Priori et al.
HEART RHYTHM (2013)
Cardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular and genetic aspects
Carol Ann Remme
JOURNAL OF PHYSIOLOGY-LONDON (2013)
Genetic testing for inherited cardiac disease
Arthur A. M. Wilde et al.
NATURE REVIEWS CARDIOLOGY (2013)
Risk of Arrhythmia and Sudden Death in Patients With Asymptomatic Preexcitation A Meta-Analysis
Manoj N. Obeyesekere et al.
CIRCULATION (2012)
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
Lia Crotti et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2012)
QTc Behavior During Exercise and Genetic Testing for the Long-QT Syndrome
Peter J. Schwartz et al.
CIRCULATION (2011)
The prevalence, distribution, and clinical outcomes of electrocardiographic repolarization patterns in male athletes of African/Afro-Caribbean origin
Michael Papadakis et al.
EUROPEAN HEART JOURNAL (2011)
Ethnic Differences in Physiological Cardiac Adaptation to Intense Physical Exercise in Highly Trained Female Athletes
J. Rawlins et al.
CIRCULATION (2010)
The Role of the Funny Current in Pacemaker Activity
Dario DiFrancesco
CIRCULATION RESEARCH (2010)
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia
Frank I. Marcus et al.
EUROPEAN HEART JOURNAL (2010)
Prevalence and significance of T-wave inversions in predominantly Caucasian adolescent athletes
Michael Papadakis et al.
EUROPEAN HEART JOURNAL (2009)
Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families
Elijah R. Behr et al.
EUROPEAN HEART JOURNAL (2008)
Left-Dominant Arrhythmogenic Cardiomyopathy
Srijita Sen-Chowdhry et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2008)
Long-term outcome and risk stratification in dilated cardiolaminopathies
Michele Pasotti et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2008)
Next-generation DNA sequencing
Jay Shendure et al.
NATURE BIOTECHNOLOGY (2008)
Brugada syndrome
Charles Antzelevitch
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY (2006)
Short QT syndrome: clinical findings and diagnostic-therapeutic implications
Carla Giustetto et al.
EUROPEAN HEART JOURNAL (2006)
Inherited conduction system abnormalities - One group of diseases, many genes
CM Wolf et al.
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY (2006)
Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling
J Ingles et al.
JOURNAL OF MEDICAL GENETICS (2005)
Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations
B Bauce et al.
EUROPEAN HEART JOURNAL (2005)
Left ventricular non-compaction - Insights from cardiovascular magnetic resonance imaging
SE Petersen et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2005)
Management of long QT syndrome
PJ Schwartz
NATURE CLINICAL PRACTICE CARDIOVASCULAR MEDICINE (2005)
Brugada syndrome - Report of the second consensus conference - Endorsed by the Heart Rhythm Society and the European Heart Rhythm Association
C Antzelevitch et al.
CIRCULATION (2005)
Does sports activity enhance the risk of sudden death in adolescents and young adults?
D Corrado et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2003)
Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)
DW Benson et al.
JOURNAL OF CLINICAL INVESTIGATION (2003)
Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy
MH Gollob et al.
CIRCULATION (2001)
Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy
R Jenni et al.
HEART (2001)
Identification of a gene responsible for familial Wolff-Parkinson-White syndrome
MH Gollob et al.
NEW ENGLAND JOURNAL OF MEDICINE (2001)
Share Paper
