Results 11 to 20 of about 347,198 (324)

Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and Phenocopies [PDF]

open access: yesJournal of Clinical Medicine, 2021
Hypertrophic cardiomyopathy (HCM) and primary restrictive cardiomyopathy (RCM) have a similar genetic background as they are both caused mainly by variants in sarcomeric genes.
Riccardo Vio   +9 more
semanticscholar   +2 more sources

Desmin-related cardiomyopathy presenting as restrictive cardiomyopathy: A case report with review of literature

open access: yesJournal of the Practice of Cardiovascular Sciences, 2016
Isolated cardiac involvement due to deposition of desmin is a rare cause of restrictive cardiomyopathy due to pathogenic mutation in desmin related genes.
Kalpana Kumari   +3 more
doaj   +2 more sources

Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype [PDF]

open access: yesCardiogenetics, 2012
Restrictive cardiomyopathy (RCM) is defined on the basis of the haemodynamic finding of restrictive ventricular physiology. However, restrictive ventricular pathophysiology is also a feature of other subtypes of cardiomyopathy, including hypertrophic ...
Juan Pablo Kaski   +4 more
doaj   +2 more sources

Clinical Outcomes and Genetic Analyses of Restrictive Cardiomyopathy in Children [PDF]

open access: yesCirculation Genomic and Precision Medicine, 2023
BACKGROUND: Restrictive cardiomyopathy in children is rare and outcomes are very poor. However, little information is available concerning genotype-outcome correlations.
H. Ishida   +16 more
semanticscholar   +2 more sources

Restrictive cardiomyopathy. Report of seven cases

open access: yesActa Pediátrica de México, 2014
Restrictive cardiomyopathy is a disease characterized by ventricular diastolic failure with elevation of end-dyastolic pressure and preserved systolic function.
Fonseca Sánchez Luis Alfonso   +2 more
doaj   +2 more sources

A Case of Rare Inherited Restrictive Cardiomyopathy With Severe Biatrial Enlargement

open access: yesJACC: Case Reports, 2019
We describe a case of inherited restrictive cardiomyopathy in a patient presenting with severe biatrial enlargement. We review the evaluation and management of restrictive cardiomyopathy with a focus on genetic etiologies.
Navid A. Nafissi, MD   +5 more
doaj   +2 more sources

Restrictive cardiomyopathy

open access: yesMedicine of Ukraine, 2017
Restrictive cardiomyopathy (RCM) is characterized by nondilated left or right ventricle with diastolic dysfunction. The restrictive cardiomyopathies are a heterogenous group of myocardial diseases that vary according to pathogenesis, clinical ...
B. Bellmann   +4 more
semanticscholar   +4 more sources

Restrictive cardiomyopathy: difficulties desminopathy diagnostics

open access: yesРоссийский кардиологический журнал, 2019
The article provides a brief overview of the problems of diagnostics and etiological verification of restrictive cardiomyopathy (RCMP). Multiple causes lead to the restrictive phenotype of intracardiac hemodynamics and diastolic dysfunction of the heart:
T. G. Vaikhanskaya   +5 more
doaj   +3 more sources

Desmin-related restrictive cardiomyopathy in a pediatric patient: A case report

open access: yesIndian Journal of Pathology and Microbiology, 2013
Restrictive cardiomyopathies in the pediatric population have diverse etiologies, including storage diseases like hemosiderosis, glycogenoses and desmin with its associated proteins.
Shruti Sharma   +4 more
doaj   +2 more sources

Restrictive cardiomyopathy. Presentation of seven cases

open access: yesActa Pediátrica de México, 2014
Restrictive cardiomyopathy is a disease characterized by diastolic ventricular failure with increase in telediastolic pressure and systolic function preserved.
Luis Alfonso Fonseca Sánchez   +2 more
doaj   +2 more sources

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