Results 1 to 10 of about 11,936 (121)
Pediatric Restrictive Cardiomyopathies [PDF]
Frontiers in Pediatrics, 2022 Restrictive cardiomyopathy (RCM) is the least frequent phenotype among pediatric heart muscle diseases, representing only 2.5–3% of all cardiomyopathies diagnosed during childhood. Pediatric RCM has a poor prognosis, high incidence of pulmonary hypertension (PH), thromboembolic events, and sudden death, is less amenable to medical or surgical treatment
Raffaello Ditaranto +13 more
openaire +3 more sources
Restrictive cardiomyopathy: from genetics and clinical overview to animal modeling
Reviews in Cardiovascular Medicine, 2022 Restrictive cardiomyopathy (RCM), a potentially devastating heart muscle disorder, is characterized by diastolic dysfunction due to abnormal muscle relaxation and myocardial stiffness resulting in restrictive filling of the ventricles.
Michelle Chintanaphol +4 more
doaj +1 more source
Multimodality Imaging Clues for Restrictive Cardiomyopathy
Journal of the Indian Academy of Echocardiography & Cardiovascular Imaging, 2022 Restrictive cardiomyopathy is an entity that can be mistaken for several mimicking conditions, including hypertrophic cardiomyopathy. These patients present with heart failure, which is essentially due to left ventricular diastolic dysfunction, with ...
Srilakshmi M Adhyapak +6 more
doaj +1 more source
Restrictive cardiomyopathies [PDF]
European Journal of Echocardiography, 2009 Restrictive cardiomyopathies constitute a heterogenous group of heart muscle conditions that all have, in common, the symptoms of heart failure. Diastolic dysfunction with preserved systolic function is often the only echocardiographic abnormality that may be noted, although systolic dysfunction may also be an integral part of some specific pathologies,
Petros, Nihoyannopoulos, David, Dawson
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Unusual case of restrictive cardiomyopathy in young
IHJ Cardiovascular Case Reports, 2022 Restrictive cardiomyopathy (RCM) is an uncommon form of cardiomyopathy and is characterized by impaired ventricular filling due to increased myocardial stiffness.
Archit Dahiya +4 more
doaj +1 more source
NON ISCHEMIC CARDIOMYOPATHY – A CASE REPORT
Liaquat Medical Research Journal, 2023 Cardiomyopathies are a group of diseases characterized by the structural and functional abnormalities of the heart muscles in the absence of other illnesses that might be responsible for the observed myocardial anomaly.
Anny Ashiq Ali Anny Ashiq Ali +1 more
doaj +1 more source
Outcomes after heart transplantation in patients with cardiac sarcoidosis
ESC Heart Failure, 2022 Background The number of patients with sarcoidosis requiring heart transplantation (HT) is increasing. The aim of this study was to evaluate outcomes of isolated HT in patients with sarcoid cardiomyopathy and compare them to recipients with non‐ischaemic
Rabea Asleh +8 more
doaj +1 more source
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2021 Background Cardiomyopathy is a common cause of atrial fibrillation (AF) and may also present as a complication of AF. However, there is a scarcity of evidence of clinical outcomes for people with cardiomyopathy and concomittant AF. The aim of the present
Benjamin J. R. Buckley +5 more
doaj +1 more source
Exercise and hypertrophic cardiomyopathy: Two incompatible entities? [PDF]
, 2020 A greater understanding of the pathogenic mechanisms underpinning hypertrophic cardiomyopathy (HCM) has translated to improved medical care and better survival of affected individuals.
Basu, J, Malhotra, A, Papadakis, M
core +1 more source
Observational Study Design in Veterinary Pathology, Part 1: Study Design [PDF]
, 2018 Observational studies are the basis for much of our knowledge of veterinary pathology and are highly relevant to the daily practice of pathology. However, recommendations for conducting pathology-based observational studies are not readily available.
Amanda P. Beck +22 more
core +10 more sources