Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome

J Moncayo-Arlandi, R Brugada - Nature Reviews Cardiology, 2017 - nature.com
The intercalated discs that connect cardiomyocytes control cell-to-cell adhesion and
communication. Several macromolecular structures (desmosomes, fascia adherens …

[HTML][HTML] Arrhythmogenic cardiomyopathy and Brugada syndrome: diseases of the connexome

E Agullo-Pascual, M Cerrone, M Delmar - FEBS letters, 2014 - Elsevier
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 …

[HTML][HTML] The Brugada syndrome: a rare arrhythmia disorder with complex inheritance

JB Gourraud, J Barc, A Thollet… - Frontiers in …, 2016 - frontiersin.org
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 …

Brugada syndrome and arrhythmogenic cardiomyopathy: overlapping disorders of the connexome?

Y Ben-Haim, A Asimaki, ER Behr - EP Europace, 2021 - academic.oup.com
Arrhythmogenic cardiomyopathy (ACM) and Brugada syndrome (BrS) are inherited diseases
characterized by an increased risk for arrhythmias and sudden cardiac death. Possible …

Relationship between arrhythmogenic right ventricular cardiomyopathy and Brugada syndrome: new insights from molecular biology and clinical implications

D Corrado, A Zorzi, M Cerrone, I Rigato… - Circulation …, 2016 - Am Heart Assoc
2 Corrado et al ARVC vs Brugada Syndrome reexcitation) leading to rapid polymorphic VT,
which can degenerate into VF (repolarization theory) 7, 8 (Figure 2). On the contrary …

[HTML][HTML] Structural heart alterations in Brugada syndrome: is it really a channelopathy? A systematic review

A Oliva, S Grassi, V Pinchi, F Cazzato, M Coll… - Journal of Clinical …, 2022 - mdpi.com
Brugada syndrome (BrS) is classified as an inherited cardiac channelopathy attributed to
dysfunctional ion channels and/or associated proteins in cardiomyocytes rather than to …

Inherited cardiac arrhythmias

PJ Schwartz, MJ Ackerman, C Antzelevitch… - Nature reviews Disease …, 2020 - nature.com
The main inherited cardiac arrhythmias are long QT syndrome, short QT syndrome,
catecholaminergic polymorphic ventricular tachycardia and Brugada syndrome. These rare …

Brugada syndrome: A general cardiologist's perspective

MM Polovina, M Vukicevic, B Banko, GYH Lip… - European Journal of …, 2017 - Elsevier
Brugada syndrome (BrS) is one of the commonest inherited primary arrhythmia syndromes
typically presenting with arrhythmic syncope or sudden cardiac death (SCD) due to …

[PDF][PDF] Illuminating the path from genetics to clinical outcome in Brugada syndrome

PG Postema, R Walsh, CR Bezzina - European heart journal, 2021 - academic.oup.com
Brugada syndrome (BrS) is a relatively rare arrhythmia disorder that can lead to sudden
cardiac death (SCD) due to ventricular tachycardia/fibrillation (VT/VF), predominantly in …

RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome

N Belbachir, V Portero, ZR Al Sayed… - European Heart …, 2019 - academic.oup.com
Abstract Aims The Brugada syndrome (BrS) is an inherited cardiac disorder predisposing to
ventricular arrhythmias. Despite considerable efforts, its genetic basis and cellular …