Arrhythmogenic cardiomyopathy (ACM) and Brugada syndrome (BrS) are inherited diseases
characterized by an increased risk for arrhythmias and sudden cardiac death. Possible …

The intercalated discs that connect cardiomyocytes control cell-to-cell adhesion and
communication. Several macromolecular structures (desmosomes, fascia adherens …

Brugada syndrome (BrS) is classified as an inherited cardiac channelopathy attributed to
dysfunctional ion channels and/or associated proteins in cardiomyocytes rather than to …

This review summarizes data in support of the notion that the cardiac intercalated disc is the
host of a protein interacting network, called “the connexome”, where molecules classically …

For the last 10 years, applying new sequencing technologies to thousands of whole exomes
has revealed the high variability of the human genome. Extreme caution should thus be …

The early course of arrhythmogenic cardiomyopathy is sometimes characterised by sudden
cardiac death due to primary electrical disease before structural disease becomes evident …

Objectives This study aimed to assess the presence of echocardiographic and
electrocardiographic similarities in patients with Brugada syndrome (BrS) and …

Brugada syndrome (BrS), an inherited arrhythmogenic disease first described in 1992, is
characterized by ST segment elevations on the electrocardiogram in the right precordium …

Brugada syndrome (BrS) has been often described as a purely electrical disease. However,
current dogma surrounding this concept has shifted to accept that BrS is associated with …

Brugada syndrome (BrS) is an inherited cardiac disorder, characterised by a typical ECG
pattern and an increased risk of arrhythmias and sudden cardiac death (SCD). BrS is a …