Results 11 to 20 of about 15,555 (263)
Педиатрическая фармакология, 2011 The authors are citing the literature data and share their own experiences of observation of two patients with cardiomyopathy associated with restrictive phenotype caused by mutations in defined genes encoding the synthesis of cardiac troponin I and ...
M.V. Tural'chuk +2 more
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Heart transplant outcomes in restrictive cardiomyopathy: UNOS registry analysis of the last three decades. [PDF]
JHLT Open, 2023 Miklin DJ, DePasquale EC.
europepmc +2 more sources
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood. [PDF]
Orphanet J Rare Dis, 2022 Muravyev A +15 more
europepmc +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
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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
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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
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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
openaire +2 more sources
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
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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
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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
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