Disease: Familial ventricular tachycardia
- 1-Year Outcomes in a Pooled Cohort of Harmony Transcatheter Pulmonary Valve Clinical Trial Participants
- 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
- A New Look at Impedance in the Electrophysiology Laboratory: Local Tissue Impedance to Identify VT Substrate
- Activation signatures for identifying critical isthmi of ventricular tachyarrhythmias
- 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
- Arrhythmic Risk Stratification among Patients with Hypertrophic Cardiomyopathy
- 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
- Asymptomatic channelopathies : Risk stratification and primary prophylaxis
- Atrial Flutter and Left Hemidiaphragmatic Paralysis in the Setting of Lyme Disease
- Atrioventricular Dissociation
- Basic and translational mechanisms in inflammatory arrhythmogenic cardiomyopathy
- Cardiac events after standard of care idecabtagene vicleucel for relapsed and refractory multiple myeloma
- 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
- Causes and clinical consequences of inappropriate shocks experienced by patients wearing a cardioverter-defibrillator
- 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 features of pediatric Danon disease and the importance of early diagnosis
- Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry
- Clinical profile and electrophysiological characteristics of atypical atrioventricular nodal reentrant tachycardia: A decade's experience
- 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
- Extracellular Kir2.1<sup>C122Y</sup> Mutant Upsets Kir2.1-PIP<sub>2</sub> Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome
- Failure to defibrillate or cardiovert due to premature truncation of biphasic shocks from implantable defibrillators
- Fractal analysis in cardiovascular magnetic resonance: prognostic value of biventricular trabecular complexity in hypertrophic cardiomyopathy
- Gene Therapy for Catecholaminergic Polymorphic Ventricular Tachycardia
- Generation of two induced pluripotent stem cell lines from catecholaminergic polymorphic ventricular tachycardia patients carrying RYR2 mutations
- Heat and cold stress increases the risk of paroxysmal supraventricular tachycardia
- Hemophagocytic Lymphohistiocytosis and Pancreatic Cancer: A Rare Association
- Importance of exercise stress testing in evaluation of unexplained cardiac arrest survivor
- In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome
- Injecting a ventricular tachycardia into the heart-alpha unique case report
- Injecting a ventricular tachycardia into the heart-Α unique case report
- 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
- 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
- Lack of the transcription factor Nfix causes tachycardia in mice sinus node and rats neonatal cardiomyocytes
- Lamin A/C cardiomyopathy presenting as high-grade atrioventricular (AV) block, atrial fibrillation, heart failure and ventricular tachycardia in a single-family cluster
- Management of Inherited Arrhythmia Syndromes: A HiRO Consensus Handbook on Process of Care
- 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
- Non-sustained Ventricular Tachycardia as a Presentation of Arrhythmogenic Right Ventricular Cardiomyopathy
- Novel pathogenic variant in LMNA gene identified in a six-generation family causing atrial cardiomyopathy and associated right atrial conduction arrhythmias
- Novel Phenotype of LMNA Variant c.154C>G Affecting Heart, Liver, and Lipid and Iron Metabolism: A Case Report
- Novel Phenotypic Effects of a Rare <em>SCN5A</em> (c.2482C>T) Mutation
- Optimizing electrophysiology studies to prevent sudden cardiac death after myocardial infarction
- Patient-specific induced pluripotent stem cell properties implicate Ca<sup>2+</sup>-homeostasis in clinical arrhythmia associated with combined heterozygous <em>RYR2</em> and <em>SCN10A</em> variants
- 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
- Preventing and Treating Torsades de Pointes in the Mother, Fetus and Newborn in the Highest Risk Pregnancies with Inherited Arrhythmia Syndromes
- 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
- Prolonged mHealth-Based Arrhythmia Monitoring in Patients With Hypertrophic Cardiomyopathy (HCM-PATCH): Protocol for a Single-Center Cohort Study
- Recurrent familial case of early childhood sudden death: Complex post mortem genetic investigations
- Reinventing Larrey's approach for epicardial mapping: The closed pericardiostomy technique
- Reversed Septal Curvature Is Associated With Nonsustained Ventricular Tachycardia in Hypertrophic Cardiomyopathy
- Risk Stratification for Sudden Cardiac Death in Repaired Tetralogy of Fallot
- RYR2-ryanodinopathies: from calcium overload to calcium deficiency
- 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
- Siblings with Gorlin-Goltz syndrome associated with cardiac tumors: a case report and review of literature
- 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 Effect of Time to Treatment With Antiarrhythmic Drugs on Survival and Neurological Outcomes in Shock Refractory Out-of-Hospital Cardiac Arrest
- The efficacy of detecting arrhythmia is higher with 7-day continuous electrocardiographic patch monitoring than with 24-h Holter monitoring
- 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
- Tools to differentiate between Filamin C and Titin truncating variant carriers: value of MRI
- 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 arrhythmias in patients with hypertrophic cardiomyopathy: Prevalence, distribution, predictors, and outcome
- Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene