Disease: Cardiac conduction defect- familial
- A case report of high-degree AV block in pregnancy
- 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
- Activation signatures for identifying critical isthmi of ventricular tachyarrhythmias
- 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
- Assessment of QT Interval Abnormalities on Electrocardiogram in Children With Breath-Holding Spells
- Asymptomatic channelopathies : Risk stratification and primary prophylaxis
- 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 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
- Causes and clinical consequences of inappropriate shocks experienced by patients wearing a cardioverter-defibrillator
- Clinical and genetic profiles of chinese pediatric patients with catecholaminergic polymorphic ventricular tachycardia
- Clinical manifestations and MRI features of Danon disease: a case series
- 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
- Diagnostic and therapeutic dilemmas in a patient with myocarditis, Brugada syndrome and arrhythmic syncope
- 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
- Elucidation of <em>ALG10B</em> as a Novel Long-QT Syndrome-Susceptibility Gene
- Errata: Rare Compound Heterozygous Missense Mutation of the SCN5A Gene with Childhood-Onset Sick Sinus Syndrome in Two Chinese Sisters: A Case Report
- 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
- 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
- Functional Characterisation of the Rare <em>SCN5A</em> p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells
- Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells
- Functional identification of hot-spot mutations in cardiac calcium channel genes associated with the J wave syndromes
- GPD1L-A306del modifies sodium current in a family carrying the dysfunctional SCN5A-G1661R mutation associated with Brugada syndrome
- Gut microbiome relationship with arrhythmias and conduction blocks: A two-sample Mendelian randomization study
- 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
- Identifying Congenital Heart Block in Primary Care
- 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
- Injecting a ventricular tachycardia into the heart-Α unique case report
- Isolated JUP plakoglobin gene mutation with left ventricular fibrosis in familial arrhythmogenic right ventricular cardiomyopathy
- Junctional Tachycardia: A Critical Reassessment
- KCNH2 mutation c.3099_3112del causes congenital long QT syndrome type 2 with gender differences
- Lamin A/C cardiomyopathy presenting as high-grade atrioventricular (AV) block, atrial fibrillation, heart failure and ventricular tachycardia in a single-family cluster
- 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
- Maternal Anti-Ro Antibody Titers Obtained With Commercially Available Immunoassays Are Strongly Associated With Immune-Mediated Fetal Heart Disease
- More than 30 years of Brugada syndrome: a critical appraisal of achievements and open issues
- Neonatal lupus erythematosus, a clinical case
- 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 NKX2.5 variant associated with congenital heart disease and increased risk of malignant arrhythmia and sudden cardiac death
- Novel p.Asp27Glu ACTA1 variant features congenital myopathy with finger flexor weakness, cardiomyopathy, and cardiac conduction defects
- 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
- Patient-specific iPSC-derived cardiomyocytes reveal variable phenotypic severity of Brugada syndrome
- 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
- Predictors and outcomes of pacemaker implantation in patients with cardiac amyloidosis
- 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
- Procainamide-Provoked Brugada Pattern in a Patient Presenting with New-Onset Atrial Fibrillation or Flutter: When Does it Matter?
- QTc prolongation with bedaquiline treatment for drug-resistant pulmonary TB in a programmatic setting
- Reinventing Larrey's approach for epicardial mapping: The closed pericardiostomy technique
- Relevance of <em>KCNJ5</em> in Pathologies of Heart Disease
- Relevance of KCNJ5 in Pathologies of Heart Disease
- 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
- 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
- Severe cardiac conduction disease associated with titin gene mutation
- Siblings with Gorlin-Goltz syndrome associated with cardiac tumors: a case report and review of literature
- The adhesion G-protein-coupled receptor mayo/CG11318 controls midgut development in Drosophila
- 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
- Two ripples in a pond: The subtleties of mapping observations in localizing premature ventricular complex sites
- 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
- Use, misuse, and pitfalls of the drug challenge test in the diagnosis of the Brugada syndrome
- 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
- Ventricular arrhythmias in patients with hypertrophic cardiomyopathy: Prevalence, distribution, predictors, and outcome
- Ventricular Conduction Stability Noninvasively Identifies an Arrhythmic Substrate in Survivors of Idiopathic Ventricular Fibrillation