Results 1 to 10 of about 27,486 (234)

Early-onset restrictive cardiomyopathy with life-threatening arrhythmia caused by a homozygous desmin mutation: a case report [PDF]

open access: yesBMC Pediatrics
Restrictive cardiomyopathy (RCM) is a rare cardiac disease characterized by the predominance of severe diastolic dysfunction, normal or mildly increased ventricular wall thickness, and either normal or mildly reduced ejection fraction.
Tianjiao Wang   +6 more
doaj   +2 more sources

Multimodality Imaging Clues for Restrictive Cardiomyopathy

open access: yesJournal 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 cardiomyopathy: from genetics and clinical overview to animal modeling

open access: yesReviews 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

Unusual case of restrictive cardiomyopathy in young

open access: yesIHJ 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

open access: yesLiaquat 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

open access: yesESC 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

Atrial Fibrillation in Patients With Cardiomyopathy: Prevalence and Clinical Outcomes From Real‐World Data

open access: yesJournal 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]

open access: yes, 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]

open access: yes, 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

Focus on Paediatric Restrictive Cardiomyopathy: Frequently Asked Questions

open access: yesDiagnostics, 2023
Restrictive cardiomyopathy (RCM) is characterized by restrictive ventricular pathophysiology determined by increased myocardial stiffness. While suspicion of RCM is initially raised by clinical evaluation and supported by electrocardiographic and ...
Mattia Zampieri   +16 more
doaj   +1 more source

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