Results 41 to 50 of about 7,984 (209)
A global perspective of arrhythmogenic right ventricular cardiomyopathy. [PDF]
, 2012 Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a progressive inherited heart disease characterized by ventricular arrhythmias and sudden cardiac death especially in the young. ARVC has been traditionally associated with the Mediterranean basin,
Alhashemi, M +3 more
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A meta-analysis for echocardiographic assessment of right ventricular structure and function in ARVC. [PDF]
, 2016 INTRODUCTION: Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is an inherited pathology that can increase the risk of sudden death. Current Task Force Criteria for echocardiographic diagnosis do not include new, regional assessment tools which may
Bhattacharrya, S +18 more
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Is arrhythmogenic right ventricular cardiomyopathy a paediatric problem too? [PDF]
, 2001 Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disease that is often familial, characterized by arrhythmias of right ventricular origin, due to transmural fatty or fibrofatty replacement of atrophic myocardium. ARVC is usually
Basso, Cristina +4 more
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Alternative Lead ECG Placements
Annals of Noninvasive Electrocardiology, Volume 31, Issue 3, May 2026.Alternative ECG lead placements can improve diagnostic yield when the standard 12‐lead ECG is suboptimal or infeasible. This review summarizes practical, scenario‐driven modifications (right‐sided, posterior, seated/prone, Lewis, Fontaine, torso‐based, and monitoring configurations) to better detect ischemia, right ventricular disease/ARVD, and ...
José Luis Morales‐Arteaga +12 more
wiley +1 more source
, 2005 Since 1995, according to the World Health Organisation’s classification of cardiomyopathies, Naxos disease has been considered as the recessive form of arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C).1 It is a stereotype association of
Protonotarios, Nikos +1 more
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Clinical Cardiology, Volume 49, Issue 4, April 2026.Methods and cohort: HF patients with normal to mild renal insufficiency (n = 637), divided into HFpEF, HFmrEF, and HFrEF. Statistical Method: Cox regression models, Kaplan‐Meier Curves, C‐index, IDI, and NRI. Findings: Over a follow‐up of 9.4 years, significant associations of elevated CysC levels with increased risks of all‐cause mortality and HF ...
Lyu Lyu +5 more
wiley +1 more source
Zdravniški Vestnik, 2019 Arrhythmogenic cardiomyopathy (AC) is a genetic disease of the myocardium characterized by fibro-fatty replacement of the apoptotic myocardium. It primarily affects the right ventricle, however in advanced stages of the disease the left ventricle can ...
Blaž Podgoršek +4 more
doaj +1 more source
Fatty images of the heart: spectrum of normal and pathological findings at computed tomography and cardiac magnetic resonance imaging. [PDF]
, 2018 Ectopic cardiac fatty images are not rarely detected incidentally at computed tomography and cardiac magnetic resonance, either in exams focused on the heart as in general thoracic imaging evaluations.
Cannavale, Giuseppe +6 more
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Veterinary Record Case Reports, Volume 14, Issue 1, February 2026.Abstract A 10‐year‐old, female, spayed Pitbull mix presented for evaluation of an arrhythmia. Echocardiography revealed enlargement of all cardiac chambers and decreased left ventricular systolic function. Electrocardiography demonstrated isolated, ventricular premature complexes.
Nathan Mitchell +3 more
wiley +1 more source
Catheter Ablation in Arrhythmic Cardiac Diseases: Endocardial and Epicardial Ablation
Reviews in Cardiovascular Medicine, 2022 Arrhythmogenic cardiomyopathy (ACM) is a group of arrhythmogenic disorders of the myocardium that are not caused by ischemic, hypertensive, or valvular heart disease.
Wen-Han Cheng +15 more
doaj +1 more source