Browsing Departament de Ciències Mèdiques by Subject "Arrhythmia"

A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome

Stop-Gain Mutations in PKP2 Are Associated with a Later Age of Onset of Arrhythmogenic Right Ventricular Cardiomyopathy

Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome

Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia

Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort

Genetics of channelopathies associated with sudden cardiac death

Transcriptional regulation of the sodium channel gene (SCN5A) by GATA4 in human heart

Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic Advances

Recent Advances in Short QT Syndrome

Trafficking and Function of the Voltage-Gated Sodium Channel β2 Subunit

Editorial: Paediatric arrhythmology: a challenge of the 21st century = Arritmología pediátrica, el reto del siglo XXI

Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes

Alterations in ubiquitin-mediated degradation of NaV 1.5 can cause arrhythmia

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?

Role of Non-Coding Variants in Brugada Syndrome

Malignant Arrhythmogenic Role Associated with RBM20: A Comprehensive Interpretation Focused on a Personalized Approach

Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in TRDN: A Comprehensive Interpretation

Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later

Epigenetic Changes Governing Scn5a Expression in Denervated Skeletal Muscle

Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants

Inflammation in the Pathogenesis of Arrhythmogenic Cardiomyopathy: Secondary Event or Active Driver?

Sex differences in long QT syndrome