Arrhythmogenic cardiomyopathy

D Corrado, C Basso, DP Judge - Circulation research, 2017 - Am Heart Assoc
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to
sudden cardiac death, particularly in young patients and athletes. Pathological features …

Molecular mechanisms of arrhythmogenic cardiomyopathy

KM Austin, MA Trembley, SF Chandler… - Nature Reviews …, 2019 - nature.com
Arrhythmogenic cardiomyopathy is a genetic disorder characterized by the risk of life-
threatening arrhythmias, myocardial dysfunction and fibrofatty replacement of myocardial …

2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy

JA Towbin, WJ McKenna, DJ Abrams, MJ Ackerman… - Heart rhythm, 2019 - Elsevier
Arrhythmogenic cardiomyopathy (ACM) is an arrhythmogenic disorder of the myocardium
not secondary to ischemic, hypertensive, or valvular heart disease. ACM incorporates a …

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership …

MJ Ackerman, SG Priori, S Willems, C Berul… - Europace, 2011 - academic.oup.com
1From Mayo Clinic, Rochester, Minnesota; 2Fondazione Salvatore Maugeri University of
Pavia, Pavia, Italy and New York University, New York, New York; 3University Hospital …

Arrhythmogenic right ventricular cardiomyopathy

C Basso, D Corrado, FI Marcus, A Nava, G Thiene - The Lancet, 2009 - thelancet.com
Arrhythmogenic right ventricular cardiomyopathy is a rare inherited heart-muscle disease
that is a cause of sudden death in young people and athletes. Causative mutations in genes …

Walking the interactome for prioritization of candidate disease genes

S Köhler, S Bauer, D Horn, PN Robinson - The American Journal of Human …, 2008 - cell.com
The identification of genes associated with hereditary disorders has contributed to improving
medical care and to a better understanding of gene functions, interactions, and pathways …

A new diagnostic test for arrhythmogenic right ventricular cardiomyopathy

A Asimaki, H Tandri, H Huang… - … England Journal of …, 2009 - Mass Medical Soc
Background The diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC) can
be challenging because the clinical presentation is highly variable and genetic penetrance …

Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene–related arrhythmogenic right ventricular …

I Rigato, B Bauce, A Rampazzo, A Zorzi… - Circulation …, 2013 - Am Heart Assoc
Background—Mutations in genes encoding for desmosomal proteins are the most common
cause of arrhythmogenic right ventricular cardiomyopathy (ARVC). We assessed the value …

The cardiac desmosome and arrhythmogenic cardiomyopathies: from gene to disease

M Delmar, WJ McKenna - Circulation research, 2010 - Am Heart Assoc
Intercellular communication is essential for proper cardiac function. Mechanical and
electrical activity need to be synchronized so that the work of individual myocytes transforms …

An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis

D Chatterjee, M Fatah, D Akdis, DA Spears… - European heart …, 2018 - academic.oup.com
Aims Arrhythmogenic right ventricular cardiomyopathy (ARVC) is characterized by right
ventricular myocardial replacement and life-threatening ventricular arrhythmias …