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Ketogenesis in arrhythmogenic cardiomyopathy [PDF]
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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
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The Many Faces of Arrhythmogenic Cardiomyopathy: An Overview
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
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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
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Arrhythmogenic Cardiomyopathy: Focus on 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
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Targeting arrhythmogenic macrophages: lessons learned from arrhythmogenic cardiomyopathy
Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiac condition characterized by cardiac remodeling and life-threatening ventricular arrhythmias.
Thassio Mesquita, Eugenio Cingolani
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Arrhythmogenic right ventricular cardiomyopathy
Kreimer, Fabienne +5 more
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Arrhythmogenic Right Ventricular Cardiomyopathy
New England Journal of Medicine, 2017Abstract 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, 2023Abstract 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
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