Disease: Cardiac conduction defect- familial
- <em>LMNA</em> -Related Dilated Cardiomyopathy: Single-Cell Transcriptomics during Patient-derived iPSC Differentiation Support Cell type and Lineage-specific Dysregulation of Gene Expression and Development for Cardiomyocytes and Epicardium-De
- A double tachycardia: Two swords do not fit in one scabbard: Double trouble
- A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish family
- A mutation in the cardiac KV7.1 channel possibly disrupts interaction with Yotiao protein
- Activation signatures for identifying critical isthmi of ventricular tachyarrhythmias
- Arrhythmias including atrial fibrillation and congenital heart disease in Kleefstra syndrome: a possible epigenetic link
- Artificial Intelligence-Enabled Electrocardiography Predicts Future Pacemaker Implantation and Adverse Cardiovascular Events
- Atypical Progeria Primarily Manifesting as Premature Cardiac Valvular Disease Segregates with LMNA-Gene Variants
- Boerhaave's Syndrome Presenting in the Setting of Third-Degree Heart Block
- Brugada syndrome in Iran: Insights from a 12-year longitudinal study
- Cardiac magnetic resonance reveals concealed structural heart disease in patients with frequent premature ventricular contractions and normal echocardiography: A systematic review
- Cardiac Resynchronization Therapy for Non-Left Bundle Branch Block: Time for Change?
- Cardiogenetics in Germany- a view and review
- Cardiovascular Screening before Sports Participation: Results of 11487 Children
- Catecholaminergic polymorphic ventricular tachycardia (and seizure) caused by a novel homozygous likely pathogenic variant in CASQ2 gene
- Catheter Ablation for Ventricular Tachycardia in Patients With Desmoplakin Cardiomyopathy
- Clinical and genetic profiles of chinese pediatric patients with catecholaminergic polymorphic ventricular tachycardia
- Clinical and genetic yield of familial screening after a sudden unexplained death at a young age
- Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants
- Clinical manifestations and MRI features of Danon disease: a case series
- Clinical outcomes of catheter ablation for atrial fibrillation, atrial flutter, and atrial tachycardia in wild-type transthyretin amyloid cardiomyopathy: a proposed treatment strategy for catheter ablation in each arrhythmia
- Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry
- Connexin43, A Promising Target to Reduce Cardiac Arrhythmia Burden in Pulmonary Arterial Hypertension
- Cost of Pacing in Pediatric Patients With Postoperative Heart Block After Congenital Heart Surgery
- Detection of a novel pathogenic variant in KCNH2 associated with long QT syndrome 2 using whole exome sequencing
- Diagnosis of Brugada Syndrome With a Sodium-Channel-Blocker Test: Who Should Be Tested? Who Should Not?
- Diverse Phenotypic Manifestations in a Family with a Novel RYR2 E4107A Variant
- Early Atherosclerosis and Conduction Defect in a Rare Case of Dunnigan Type Familial Partial Lipodystrophy
- Effects of cohort, genotype, variant, and maternal β-blocker treatment on foetal heart rate predictors of inherited long QT syndrome
- Electrocardiographic predictors of left ventricular scar in athletes with right bundle branch block premature ventricular beats
- Electrogram Annotation and Visualization of Deceleration Zones: Finding the VT Circuit Somewhere Over the Rainbow
- Errata: Rare Compound Heterozygous Missense Mutation of the SCN5A Gene with Childhood-Onset Sick Sinus Syndrome in Two Chinese Sisters: A Case Report
- Establishment of human embryonic stem cell lines carrying LQT1 mutations by CRISPR base editing
- Evaluating the prescribing and monitoring of medications associated with QTc-prolongation in the ambulatory care setting
- Evaluation of Suspected Cardiac Arrhythmia
- Experience of treating congenital complete atrioventricular block with epicardial pacemaker in infants and young children: a retrospective study
- 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
- Feasibility, Efficacy, and Safety of Fluoroless Ablation of VT in Patients With Structural Heart Disease
- Functional and clinical characterization of a novel homozygous KCNH2 missense variant in the pore region of Kv11.1 leading to a viable but severe long-QT syndrome
- GPD1L-A306del modifies sodium current in a family carrying the dysfunctional SCN5A-G1661R mutation associated with Brugada syndrome
- Healthcare Big Data in Hong Kong: Development and Implementation of Artificial Intelligence-Enhanced Predictive Models for Risk Stratification
- Heat and cold stress increases the risk of paroxysmal supraventricular tachycardia
- High prevalence and distinctive clinical features of LMNA-associated atrioventricular block in young patients
- Home monitoring of fetal heart rhythm: Lived experiences of women with anti-SSA/Ro52 autoantibodies and their co-parents
- Impact of DCM-Causing Genetic Background on Long-Term Response to Cardiac Resynchronization Therapy
- In silico analysis of TRPM4 variants of unknown clinical significance
- In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome
- Investigation of a Large Kindred Reveals Cardiac Calsequestrin (CASQ2) as a Cause of Brugada Syndrome
- 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 Freedom From Ventricular Arrhythmias in ARVC With Endocardial Only Ablation: Predictors of Success
- Loss of sodium current caused by a Brugada syndrome-associated variant is determined by patient-specific genetic background
- 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
- MICRA AV implantation after transcatheter aortic valve replacement
- Molecular Autopsy With Banked Cord Blood Reveals Brugada Syndrome in Past Sudden Death Case
- More than 30 years of Brugada syndrome: a critical appraisal of achievements and open issues
- Multisite Validation of a Functional Assay to Adjudicate <em>SCN5A</em> Brugada Syndrome-Associated Variants
- Non-Coding RNAs and Gut Microbiota in the Pathogenesis of Cardiac Arrhythmias: The Latest Update
- Noninvasive Vagus Nerve Stimulation in Postural Tachycardia Syndrome: A Randomized Clinical Trial
- Novel combinations of variations in KCNQ1 were associated with patients with long QT syndrome or Jervell and Lange-Nielsen syndrome
- Novel compound heterozygous variants in EMC1: Overlapping phenotypes of left ventricular noncompaction and long QT syndrome warranting in-depth exploration
- Novel NKX2.5 variant associated with congenital heart disease and increased risk of malignant arrhythmia and sudden cardiac death
- Nuclear envelope lamin-related dilated cardiomyopathy: a case series including histopathology
- Patient-specific iPSC-derived cardiomyocytes reveal variable phenotypic severity of Brugada syndrome
- Pediatric and Familial Genetic Arrhythmia Syndromes-Evaluation of Prolonged QTc-Differential Diagnosis and what You Need to Know
- Pediatric and Familial Genetic Arrhythmia Syndromes: Evaluation of Bidirectional Ventricular Tachycardia-Differential Diagnosis
- Pediatric and Familial Genetic Arrhythmia Syndromes: SCN5A-Related Disorders When It Is Not Long QT Type 3: Clinical Signs and Symptoms
- Perivascular Basal Echogenicity in the Fetal Heart: An Unconventional Marker of Maternal Autoimmune Antibodies
- Phenotypic Variability of Andersen-Tawil Syndrome Due to Allelic Mutation c.652C>T in the KCNJ2 Gene-A New Family Case Report
- Prevalence and Clinical Significance of Electrocardiographic Complete Right Bundle Branch Block in Young Individuals
- Prevalence of transthyretin amyloid cardiomyopathy in pacemaker patients
- Primary Electrical Heart Disease-Principles of Pathophysiology and Genetics
- PRKAG2 syndrome, a rare hypertrophic cardiomyopathy: a Brazilian long-term follow-up with extracardiac disorders
- Procainamide-Provoked Brugada Pattern in a Patient Presenting with New-Onset Atrial Fibrillation or Flutter: When Does it Matter?
- Rare Variant in MRC2 Associated With Familial Supraventricular Tachycardia and Wolff-Parkinson-White Syndrome
- Reduced kinase function in two ultra-rare TNNI3K variants in families with congenital junctional ectopic tachycardia
- Repolarization Dispersion and Phase 2 Re-Entry: One Step Closer to Deciphering Brugada Syndrome?
- Repotrectinib in a Patient With <em>NTRK</em> Fusion-Positive Pancreatic Carcinoma and Congenital Long QT Syndrome
- Reversed Septal Curvature Is Associated With Nonsustained Ventricular Tachycardia in Hypertrophic Cardiomyopathy
- 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
- SCN5A mutation is associated with a higher Shanghai Score in patients with type 1 Brugada ECG pattern
- SCN5A-L256del and L1621F exhibit loss-of-function properties related to autosomal recessive congenital cardiac disorders presenting as sick sinus syndrome, dilated cardiomyopathy, and sudden cardiac death
- Ser194Leu DSG2 mutation, associated with arrhythmogenic left ventricular cardiomyopathy and ventricular tachycardia
- The adhesion G-protein-coupled receptor mayo/CG11318 controls midgut development in Drosophila
- 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 Relationship between Depression Symptoms and Physical Activity in Children with Idiopathic Ventricular Extrasystoles
- The W101C <em>KCNJ5</em> Mutation Induces Slower Pacing by Constitutively Active GIRK Channels in hiPSC-Derived Cardiomyocytes
- Transient second-degree type 2 atrioventricular block after infliximab infusion in a patient with Crohn's disease and heterozygous familial hypercholesterolemia
- Triglicerydes/high-density lipoprotein ratio as a risk factor of post-Covid-19 sinus tachycardia: A retrospective study
- Type 3 long QT syndrome: Is the effectiveness of treatment with beta-blockers population-specific?
- Unraveling Complexities in Genetically Elusive Long QT Syndrome
- Unravelling Novel <em>SCN5A</em> Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights
- Utility and acceptability of remote 6-lead electrocardiographic monitoring in children with inherited cardiac conditions
- Utility of Very High-Output Pacing to Identify VT Circuits in Patients Manifesting Traditionally Inexcitable Scar
- Variable clinical expression of a novel FLNC truncating variant in a large family
- Variable Penetrance and Expressivity of a Rare Pore Loss-of-Function Mutation (p.L889V) of Nav1.5 Channels in Three Spanish Families
- Vigorous Exercise in Patients With Congenital Long QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS Study