Results 31 to 40 of about 570,477 (309)

Restrictive cardiomyopathies [PDF]

open access: yesEuropean 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

Left ventricular strain‐curve morphology to distinguish between constrictive pericarditis and restrictive cardiomyopathy

open access: yesESC Heart Failure, 2021
To distinguish between constrictive pericarditis (CP) and restrictive cardiomyopathy (RCM) using cardiac magnetic resonance feature tracking (CMR‐FT) left ventricle (LV) diastolic time–strain curve patterns and myocardial strain.
Zhiyun Yang   +9 more
semanticscholar   +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

Outcomes of Restrictive Cardiomyopathy in Japanese Children - A Retrospective Cohort Study.

open access: yesCirculation Journal, 2021
BACKGROUND There has been no nationwide survey on the prognosis of pediatric restrictive cardiomyopathy (RCM) in Japan; therefore, this retrospective multicentered study was designed to investigate the long-term survival rate of pediatric patients with ...
Hiroki Mori   +8 more
semanticscholar   +1 more source

A homozygous nonsense mutation in DCBLD2 is a candidate cause of developmental delay, dysmorphic features and restrictive cardiomyopathy

open access: yesScientific Reports, 2021
DCBLD2 encodes discodin, CUB and LCCL domain-containing protein 2, a type-I transmembrane receptor that is involved in intracellular receptor signalling pathways and the regulation of cell growth.
Kheloud M. Alhamoudi   +10 more
semanticscholar   +1 more source

Left and Right Myocardial Functionality Assessed by Two-Dimensional Speckle-Tracking Echocardiography in Cats with Restrictive Cardiomyopathy

open access: yesAnimals, 2021
Simple Summary The endomyocardial form of restrictive cardiomyopathy, a primary disorder of the myocardium, is one of the diseases with poor prognosis in cats.
R. Suzuki   +5 more
semanticscholar   +1 more source

Overview of Restrictive Cardiomyopathies

open access: yesMethodist DeBakey Cardiovascular Journal, 2022
Restrictive cardiomyopathy (RCM) includes a heterogeneous group of diseases that cause increased myocardial stiffness, leading to impaired ventricular relaxation and severe diastolic dysfunction. Given that it is the least common type of cardiomyopathy, it can be a diagnostic challenge due to its varied pathogenesis, clinical presentation, and ...
Smitha Narayana Gowda   +2 more
openaire   +3 more sources

Restrictive Cardiomyopathy: A Rare Presentation of Gaucher Disease

open access: yesAnnals of African medicine, 2021
Restrictive cardiomyopathy is an unusual form of cardiomyopathy accounting only for 2%–5% of all pediatric cardiomyopathies. It is mostly idiopathic. Gaucher disease in association with restrictive cardiomyopathy is extremely rare.
Soumi Kundu   +3 more
semanticscholar   +1 more source

Generation of three TTN knock-out human induced pluripotent stem cell lines using CRISPR/Cas9 system

open access: yesStem Cell Research, 2022
TTN mutations are the common genetic cause for various types of cardiomyopathies (e.g., dilated cardiomyopathy, hypertrophic cardiomyopathy, restrictive cardiomyopathy, and arrhythmogenic right ventricular cardiomyopathy) and skeletal myopathies.
Ji-Young Kang   +7 more
doaj   +1 more source

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