• A Case Report of Brugada Syndrome Associated With Physical Trauma
• A new classification of iron-deficient heart failure, sex-related differences in the management of atrial fibrillation and mitral regurgitation, and an update on the genetics of Brugada syndrome
• A Novel Workflow for Electrophysiology Studies in Patients with Brugada Syndrome
• A Pediatric Case of Refractory Torsades de Pointes in Autoimmune Hypothyroidism
• A rare case of delayed right atrial lead perforation in an adolescent patient with Brugada syndrome
• A Rare Manifestation of Brugada ECG Pattern Precipitated by General Anesthesia for Pituitary Surgery
• A representative case of quinidine's therapeutic effect on Brugada syndrome and the negative impact of the lack of availability in some countries, with a brief note on the lack of benefit of cilostazol
• Advances and Challenges in the Management of Brugada Syndrome: A Comprehensive Review
• Applying Artificial Intelligence for Phenotyping of Inherited Arrhythmia Syndromes
• Brugada phenocopy vs. Brugada syndrome: Delineating the differences for optimal diagnosis and management
• Brugada Phenotype Following a Cocaine Overdose
• Brugada Syndrome and Pulmonary Atresia with Intact Interventricular Septum: Fortuitous Finding or New Genetic Connection?
• Brugada Syndrome and Sudden Cardiac Death: An Electrocardiographic History
• Brugada syndrome following febrile episode caused by malarial infection: a case report
• Brugada syndrome in a patient with AKAP9 mutation: Case report and review of the literature
• Brugada Syndrome in a Transplanted Heart: Implications for Organ Transplant Screening Process
• Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci
• Brugada syndrome: a review and the role of epicardial ablation in management
• Brugada syndrome: can polygenic risk scores help the clinician?
• Brugada Syndrome: Focus for the General Pediatrician
• Brugada syndrome: identification of subjects at risk and therapy
• Can Hyperthermia Unveil Brugada Pattern?
• Cardiac channelopathies in the context of hereditary arrhythmia syndromes
• Case Report: Comprehensive evaluation of ECG phenotypes and genotypes in a family with Brugada syndrome carrying SCN5A-R376H
• Case Report: Lacosamide unmasking SCN5A-associated Brugada syndrome in a young female with epilepsy
• Catheter ablation as an adjunctive therapy to ICD implantation in Brugada syndrome
• Catheter Ablation for Channelopathies: When Is Less More?
• Catheter ablation in Brugada syndrome: are we missing an opportunity?
• Clinical differences between drug-induced type 1 Brugada pattern and syndrome
• Complete mitochondrial genomes of patients from Thailand with cardiovascular diseases
• Congenial short QT syndrome: A review focused on electrocardiographic features
• Correction to "In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome"
• Correction to: An autoantibody profile detects Brugada syndrome and identifies abnormally expressed myocardial proteins
• Correction to: Implantable loop recorders in patients with Brugada syndrome: the BruLoop study
• Correlations of ventricular fibrillation and monomorphic ventricular tachycardia with SCN5A mutations and other clinical variables in Brugada syndrome
• Deceptive Anteroseptal ST-segment Elevation and Brugada Pattern Caused by Isolated Conus Artery Occlusion
• Demonstration of Arrhythmia Substrate-Associated Dispersion of Repolarization by Epicardial Unipolar Mapping in Brugada Syndrome
• Diagnosis of Brugada syndrome affects quality of life and psychological status
• Diagnosis of Brugada Syndrome With a Sodium-Channel-Blocker Test: Who Should Be Tested? Who Should Not?
• Digital precision medicine in rhythmology : Risk prediction of recurrences, sudden cardiac death, and outcome
• Electrocardiographic abnormalities are frequently detected in healthy adult Borzoi with a normal echocardiogram
• Electrophysiological patterns and structural substrates of Brugada syndrome: Critical appraisal and computational analyses
• Evaluation of the ODISEA APP for improving a STEMI regional network
• Evolving Use of Quinidine in the Treatment of Ventricular Arrhythmias
• Exercise-Induced QRS Prolongation in Brugada Syndrome: Implications for Improving Disease Phenotyping and Diagnosis
• Exercise-induced type 1 Brugada pattern in a child
• Expanding the Phenotype of the CACNA1C-Associated Neurological Disorders in Children: Systematic Literature Review and Description of a Novel Mutation
• Generation of an induced pluripotent stem cell line from a Brugada syndrome patient carrying SCN5A/c.3118G>C mutation
• Genomic analysis of an Ecuadorian individual carrying an SCN5A rare variant
• Human Genetics of Cardiac Arrhythmias
• Human Genetics of Ventricular Septal Defect
• Identification of a SCN5A Genetic Variant Associated With Type 1 Brugada Syndrome (BrS) in a Family
• Implantable loop recorders in Brugada syndrome: symptoms and arrhythmia characterization
• Implantable loop recorders in patients with Brugada syndrome: the importance of a correct patient stratification
• In-vitro studies of the NaV1.5 S805L Brugada mutation: The resting cell voltage is a critical element in determining the pathological or physiological phenotype of the current
• Investigating cardiac genetic background in sudden infant death syndrome (SIDS)
• Investigation of a Large Kindred Reveals Cardiac Calsequestrin (CASQ2) as a Cause of Brugada Syndrome
• Ion Channel Diseases as a Cause of Sudden Cardiac Death in Young People: Aspects of Their Diagnosis, Treatment, and Pathogenesis
• Late Gadolinium Enhancement in Early Repolarization Syndrome
• Lessons on the non-linear path of medical progress and biological complexity from mouse models of the Brugada syndrome
• Long-term follow-up of patients with Brugada syndrome: Foremost risk factors associated with overall arrhythmic events
• Lower Extremity Peripheral Nerve Blocks for Post-operative Pain Control in a Multi-trauma Patient With Brugada Syndrome: A Literature Review and Case Report
• Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias
• Molecular Autopsy With Banked Cord Blood Reveals Brugada Syndrome in Past Sudden Death Case
• Molecular Pathways and Animal Models of Arrhythmias
• Multimodal Mapping of Electrical and Mechanical Latency of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocyte Layers
• Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome-Associated Variants
• NaV1.5 autoantibodies in Brugada syndrome: pathogenetic implications
• New focus on cardiac voltage-gated sodium channel β1 and β1B: Novel targets for treating and understanding arrhythmias?
• No beneficial use of the wearable cardioverter defibrillator among patients suffering from inherited and congenital heart disease: data from a European multicenter registry
• Noninvasive Testing for Brugada Syndrome
• Novel Gain-of-Function Mutation in the Kv11.1 Channel Found in the Patient with Brugada Syndrome and Mild QTc Shortening
• Pediatric and Familial Genetic Arrhythmia Syndromes: SCN5A-Related Disorders When It Is Not Long QT Type 3: Clinical Signs and Symptoms
• Pericarditis prophylactic therapy after sinus node-sparing hybrid ablation for inappropriate sinus tachycardia/postural orthostatic sinus tachycardia
• Predicting and Recognizing Drug-Induced Type I Brugada Pattern Using ECG-Based Deep Learning
• Predicting ventricular arrhythmia inducibility in ajmaline-induced Brugada type I pattern: Validation of the dST-Tiso interval
• PRKAG2 syndrome, a rare hypertrophic cardiomyopathy: a Brazilian long-term follow-up with extracardiac disorders
• Proarrhythmic drugs, drug levels, and polypharmacy in victims of sudden arrhythmic death syndrome: An autopsy-based study from Denmark
• Quinidine for ventricular arrhythmias: a comprehensive review
• Relationship Between Brugada Syndrome and Ischemic Stroke: A Case Report and Comprehensive Literature Review
• Reply to the editor - Revisiting the Prognostic Role of SCN5A in Brugada Syndrome
• Repolarization Dispersion and Phase 2 Re-Entry: One Step Closer to Deciphering Brugada Syndrome?
• Requirement of beta subunit for the reduced voltage-gated Na(+) current of a Brugada syndrome patient having novel double missense mutation (p.A385T/R504T) of SCN5A
• Results of comprehensive genetic testing in patients presenting to a multidisciplinary inherited heart disease clinic in India
• Revisiting the Prognostic Role of SCN5A in Brugada Syndrome
• Risk Stratification for the Occurrence of Ventricular Fibrillation in Patients with Early Repolarization Syndrome
• SCN5A gene variants and arrhythmic risk in Brugada syndrome: An updated systematic review and meta-analysis
• Septal Artery Strangulation Causing Brugada Phenocopy: A Rare Presentation
• Syncope and Brugada-Like ECG Pattern in a Patient with Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)
• Systematic analysis of SCN5A variants associated with inherited cardiac diseases
• Temperature and ST-segment morphology remote monitoring: new perspectives for implantable cardiac monitors in Brugada syndrome
• The complex interaction between cancer, ischaemic heart disease, and heart failure, and a focus on arrhythmias including risk stratification in Brugada syndrome and leadless pacing
• The importance of variant reinterpretation in inherited cardiovascular diseases: Establishing the optimal timeframe
• The Role for Ambulatory ECG monitoring in the Diagnosis and Prognostication of Brugada Syndrome: A sub-study of the Rare Arrhythmia Syndrome Evaluation (RASE) Brugada Study
• The role for ambulatory electrocardiogram monitoring in the diagnosis and prognostication of Brugada syndrome: a sub-study of the Rare Arrhythmia Syndrome Evaluation (RASE) Brugada study
• The role of GPD1L, a sodium channel interacting gene, in the pathogenesis of Brugada Syndrome
• Type 1 Brugada Pattern May Be Provoked by Ajmaline in Some Healthy Subjects: Results From a Clinical Trial
• Unconventional diagnosis of bradyarrhythmic syncope in Brugada syndrome: a case report
• Valvulopathies and Genetics: Where are We?
• Variable Penetrance and Expressivity of a Rare Pore Loss-of-Function Mutation (p.L889V) of Nav1.5 Channels in Three Spanish Families