• 18-Month-Old with Lethargy and Accelerated Idioventricular Rhythm in Prehospital Setting: A Case Report
• A case of Carvajal syndrome presenting with dilated cardiomyopathy
• A double tachycardia: Two swords do not fit in one scabbard: Double trouble
• Activation signatures for identifying critical isthmi of ventricular tachyarrhythmias
• An Interesting Case of Wolf-Parkinson-White Syndrome in a Young Patient With Sensorineural Deafness
• An International Multicenter Cohort Study on Implantable Cardioverter Defibrillators for the Treatment of Symptomatic Children with Catecholaminergic Polymorphic Ventricular Tachycardia
• An international multicenter cohort study on implantable cardioverter-defibrillators for the treatment of symptomatic children with catecholaminergic polymorphic ventricular tachycardia
• Arrhythmias including atrial fibrillation and congenital heart disease in Kleefstra syndrome: a possible epigenetic link
• Arrhythmogenic mechanism of a novel ryanodine receptor mutation underlying sudden cardiac death
• Arrhythmogenic Right Ventricular Cardiomyopathy
• Assessment of Sudden Cardiac Death Risk in Pediatric Primary Electrical Disorders: A Comprehensive Overview
• Association of coronary angiography with ST-elevation and no ST-elevation in patients with refractory ventricular fibrillation - A substudy of the DOuble SEquential External Defibrillation for Refractory Ventricular Fibrillation (DOSE-VF randomized contro
• Associations between Selected <em>ADRB1</em> and <em>CYP2D6</em> Gene Polymorphisms in Children with Ventricular and Supraventricular Arrhythmias
• Associations between Selected ADRB1 and CYP2D6 Gene Polymorphisms in Children with Ventricular and Supraventricular Arrhythmias
• Atrioventricular Dissociation
• Basic and translational mechanisms in inflammatory arrhythmogenic cardiomyopathy
• Cardiac Resynchronization Therapy for Non-Left Bundle Branch Block: Time for Change?
• Cardiomyopathy Imaging
• Cardiovascular Screening before Sports Participation: Results of 11487 Children
• Carnitine palmitoyltransferase II (CPT II) deficiency responsible for refractory cardiac arrhythmias, acute multiorgan failure and early fatal outcome
• Case Report: Comprehensive evaluation of ECG phenotypes and genotypes in a family with Brugada syndrome carrying SCN5A-R376H
• Case Report: Four cases of cardiac sarcoidosis in patients with inherited cardiomyopathy-a phenotypic overlap, co-existence of two rare cardiomyopathies or a second-hit disease
• Case Report: Multiple types of arrhythmias in a late-confirmed Danon disease
• Catecholaminergic polymorphic ventricular tachycardia (and seizure) caused by a novel homozygous likely pathogenic variant in CASQ2 gene
• Catecholaminergic Polymorphic Ventricular Tachycardia: A Review of Therapeutic Strategies
• Catheter Ablation for Ventricular Tachycardia in Patients With Desmoplakin Cardiomyopathy
• Characterization of cardiac involvement in patients with <em>LMNA</em> splice-site mutation-related dilated cardiomyopathy and sudden cardiac death
• Clinical and genetic analysis of five children with Catecholaminergic polymorphic ventricular tachycardia due to variants of RYR2 gene
• Clinical and Genetic Characteristics of Arrhythmogenic Right Ventricular Cardiomyopathy Patients: A Single-Center Experience
• Clinical and genetic characteristics of catecholaminergic polymorphic ventricular tachycardia combined with left ventricular non-compaction
• Clinical and genetic profiles of chinese pediatric patients with catecholaminergic polymorphic ventricular tachycardia
• Clinical Characteristics of Primary Biliary Cirrhosis - Idiopathic Inflammatory Myopathy Overlap Syndrome: a Single Center Study
• Clinical exome sequencing unravels the diverse spectrum of genetic heterogeneity and genotype-phenotype correlations in hypertrophic cardiomyopathy
• Clinical features of pediatric Danon disease and the importance of early diagnosis
• Clinical Insights in RNA-Binding Protein Motif 20 Cardiomyopathy: A Systematic Review
• Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry
• Clinical profile and electrophysiological characteristics of atypical atrioventricular nodal reentrant tachycardia: A decade's experience
• Current US prevalence of myocardial injury patterns and clinical outcomes among hospitalised patients with familial hypercholesterolaemia: insight from the National Inpatient Sample-a retrospective cohort study
• Diverse Phenotypic Manifestations in a Family with a Novel RYR2 E4107A Variant
• Electrical Storm/Refractory Ventricular Tachycardia
• Electrogram Annotation and Visualization of Deceleration Zones: Finding the VT Circuit Somewhere Over the Rainbow
• Emergency Medicine Perspectives: The Importance of Bystanders and Their Impact on On-Site Resuscitation Measures and Immediate Outcomes of Out-of-Hospital Cardiac Arrest
• Evaluation and Management of Sudden Death Risk in Repaired Tetralogy of Fallot
• Evolution of Substrate for Ventricular Arrhythmias Early Postinfarction: Insights From a Porcine Ischemia-Reperfusion Model
• Extracellular Kir2.1^C122Y Mutant Upsets Kir2.1-PIP₂ Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome
• Failure to defibrillate or cardiovert due to premature truncation of biphasic shocks from implantable defibrillators
• Feasibility, Efficacy, and Safety of Fluoroless Ablation of VT in Patients With Structural Heart Disease
• Fractal analysis in cardiovascular magnetic resonance: prognostic value of biventricular trabecular complexity in hypertrophic cardiomyopathy
• Heat and cold stress increases the risk of paroxysmal supraventricular tachycardia
• Hemophagocytic Lymphohistiocytosis and Pancreatic Cancer: A Rare Association
• Human Genetics of Cardiac Arrhythmias
• Identification of a SCN5A Genetic Variant Associated With Type 1 Brugada Syndrome (BrS) in a Family
• Identifying the Method Preceding the Madness: Can it Advance Treatment Strategies?
• In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome
• Intraoperative Acute Cardiac Tamponade as a Result of Intracardiac Perforation Requiring Emergency Continuous Pericardiocentesis and Open Sternotomy: A Case Report and Literature Review of a Rare but Fatal Complication
• Ion Channel Diseases as a Cause of Sudden Cardiac Death in Young People: Aspects of Their Diagnosis, Treatment, and Pathogenesis
• Isolated JUP plakoglobin gene mutation with left ventricular fibrosis in familial arrhythmogenic right ventricular cardiomyopathy
• KCNH2 mutation c.3099_3112del causes congenital long QT syndrome type 2 with gender differences
• Long-Term Arrhythmic Follow-Up and Risk Stratification of Patients With Desmoplakin-Associated Arrhythmogenic Right Ventricular Cardiomyopathy
• Long-Term Freedom From Ventricular Arrhythmias in ARVC With Endocardial Only Ablation: Predictors of Success
• Magnetic Resonance Imaging Characterization and Clinical Outcomes of Dilated and Arrhythmogenic Left Ventricular Cardiomyopathies
• Management of patients with an electrical storm or clustered ventricular arrhythmias: a clinical consensus statement of the European Heart Rhythm Association of the ESC-endorsed by the Asia-Pacific Heart Rhythm Society, Heart Rhythm Society, and Latin-Ame
• Mitral annular disjunction on cardiac MRI: Prevalence and association with disease severity in Loeys-Dietz syndrome
• Novel pathogenic variant in LMNA gene identified in a six-generation family causing atrial cardiomyopathy and associated right atrial conduction arrhythmias
• Novel Phenotypic Effects of a Rare <em>SCN5A</em> (c.2482C&gt;T) Mutation
• Optimizing electrophysiology studies to prevent sudden cardiac death after myocardial infarction
• Pediatric and Familial Genetic Arrhythmia Syndromes: Evaluation of Bidirectional Ventricular Tachycardia-Differential Diagnosis
• Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy
• Post-myocardial infarction treatment with resiniferatoxin modulates the expression of important genes involved in inflammation, plaque stability and angiogenesis
• Post-operative arrest following pectus excavatum repair: A case report with a systematic review of the published case reports
• Primary Electrical Heart Disease-Principles of Pathophysiology and Genetics
• Procedural Adaptations to Avoid Haemodynamic Instability During Catheter Ablation of Scar-related Ventricular Tachycardia
• Prognosis and clinical management of asymptomatic family members with RYR2-mediated catecholaminergic polymorphic ventricular tachycardia: a review
• Prognostic value of myocardial deformation parameters for outcome prediction in tetralogy of Fallot
• Prolonged mHealth-Based Arrhythmia Monitoring in Patients With Hypertrophic Cardiomyopathy (HCM-PATCH): Protocol for a Single-Center Cohort Study
• Re-examining family history of sudden death as a risk marker in hypertrophic cardiomyopathy
• Recurrent familial case of early childhood sudden death: Complex post mortem genetic investigations
• Reversed Septal Curvature Is Associated With Nonsustained Ventricular Tachycardia in Hypertrophic Cardiomyopathy
• Rising Cardiovascular Mortality Despite Increased Resource Utilization: Insights From the Nationwide Inpatient Sample Database
• Risk Stratification for Sudden Cardiac Death in Repaired Tetralogy of Fallot
• Risk Stratification in Cardiac Sarcoidosis With Cardiac Positron Emission Tomography: A Systematic Review and Meta-Analysis
• Role of new generation implantable loop recorders in managing undiagnosed pediatric cardiac symptoms
• SARS-CoV-2 Infection Precipitating VT Storm in Patients With Cardiac Sarcoidosis
• Scar architecture affects the electrophysiological characteristics of induced ventricular arrhythmias in hypertrophic cardiomyopathy
• Septal Substrate Ablation Guided by Delayed Transmural Conduction Times: A Novel Ablation Approach to Target Intramural Substrates
• Ser194Leu DSG2 mutation, associated with arrhythmogenic left ventricular cardiomyopathy and ventricular tachycardia
• Sudden Death in Athletes
• Targeting NLRP3 signaling reduces myocarditis-induced arrhythmogenesis and cardiac remodeling
• The Beneficial Role of Telemedicine for Arrhythmic Risk Stratification in Asymptomatic Brugada Syndrome: An Exemplary Case Report
• The Novel Familial ST-Depression Syndrome - Current Knowledge and Perspectives
• The phenotypic and genetic features of arrhythmogenic cardiomyopathy in the pediatric population
• The role of detailed medical history for the early diagnosis of familial bradycardia in a patient with associated atrial fibrillation: case report
• The role of genetic testing in the prevention, diagnosis, and prognosis of sudden cardiac arrest in children
• The VINTAGE Approach: Is Direct Intramyocardial Ablation Finally "Coming of Age"?
• Type 3 long QT syndrome: Is the effectiveness of treatment with beta-blockers population-specific?
• Unravelling Novel <em>SCN5A</em> Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights
• Utility of Very High-Output Pacing to Identify VT Circuits in Patients Manifesting Traditionally Inexcitable Scar
• Ventricular Angiography: A Forgotten Diagnostic Tool?
• Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene
• Young patient presenting with cardiogenic shock and refractory ventricular tachycardia: a case of unsuspected arrhythmogenic cardiomyopathy leading to urgent heart transplantation