Results 61 to 70 of about 979 (102)

Genotype-phenotype correlations in patients with pathogenic/likely pathogenic titin variants from the Swiss Arrhythmogenic Cardiomyopathy Registry

open access: yesOpen Heart
Background Truncating variants in the titin gene (TTNtv) are associated with cardiomyopathy, mainly dilated cardiomyopathy (DCM). The clinical presentation and outcomes of arrhythmogenic phenotypes in these patients are scarcely studied.Methods and ...
Andreas J Flammer   +19 more
doaj   +1 more source

The Many Faces of Arrhythmogenic Cardiomyopathy: An Overview

open access: yesThe Application of Clinical Genetics, 2023
Hanna J Tadros,1 Christina Y Miyake,1,2 Debra L Kearney,3 Jeffrey J Kim,1 Susan W Denfield4 1Department of Pediatrics, Section of Pediatric Cardiology, Texas Children’s Hospital, Baylor College of Medicine, Houston, TX, USA; 2Department of Molecular ...
Tadros HJ   +4 more
doaj  

Natural Course of Electrocardiographic Features in Arrhythmogenic Right Ventricular Cardiomyopathy and Their Relation to Ventricular Arrhythmic Events

open access: yesJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Electrocardiographic abnormalities are common in arrhythmogenic right ventricular cardiomyopathy and are included in the 2010 Task Force Criteria. Their time course, however, remains uncertain.
Anneli Svensson   +11 more
doaj   +1 more source

Arrhythmogenic Cardiomyopathy

open access: yes, 2011
n ...
Pilichou, Kalliopi   +3 more
openaire   +1 more source

Arrhythmogenic Cardiomyopathy: Focus on Imaging

open access: yesJournal of the Indian Academy of Echocardiography & Cardiovascular Imaging
Arrhythmogenic cardiomyopathy (AC) is a broad term denoting subclinical or clinical heart muscle disease which presents predominantly with serious arrhythmias.
Madhu Shukla   +3 more
doaj   +1 more source

Targeting arrhythmogenic macrophages: lessons learned from arrhythmogenic cardiomyopathy

open access: yesThe Journal of Clinical Investigation
Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiac condition characterized by cardiac remodeling and life-threatening ventricular arrhythmias.
Thassio Mesquita, Eugenio Cingolani
doaj   +1 more source

Arrhythmogenic right ventricular cardiomyopathy

open access: yesDeutsches Ärzteblatt international
Kreimer, Fabienne   +5 more
openaire   +2 more sources

Arrhythmogenic Right Ventricular Cardiomyopathy

New England Journal of Medicine, 2017
Abstract Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heredo-familial heart muscle disease characterized by progressive myocardial atrophy with fibrofatty replacement. It is a rare disease with an estimated prevalence of 1:2000 to 1:5000.

exaly   +6 more sources

Diagnostic delay in arrhythmogenic cardiomyopathy

European Journal of Preventive Cardiology, 2023
Abstract Aims Diagnosis of arrhythmogenic cardiomyopathy (ACM) may be challenging, as it comprises diverse phenotypes (right dominant, biventricular, and left dominant), and each may overlap with other clinical entities.
Giacomo Tini   +11 more
openaire   +4 more sources

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