Histone lysine methyltransferase SETD2 regulates coronary vascular development in embryonic mouse hearts

F Chen, J Chen, H Wang, H Tang, L Huang… - Frontiers in Cell and …, 2021 - frontiersin.org
Congenital heart defects are the most common birth defect and have a clear genetic
component, yet genomic structural variations or gene mutations account for only a third of …

[HTML][HTML] Echocardiographic characteristics of isolated left ventricular noncompaction

A Fazlinezhad, M Vojdanparast, S Sarafan… - ARYA …, 2016 - ncbi.nlm.nih.gov
BACKGROUND Although isolated left ventricular noncompaction (ILVNC) has been
described almost two decades ago, our knowledge about its diagnosis, presentation …

Pathophysiology of cardiomyopathies

H Saini, S Tabtabai, JR Stone, PT Ellinor - Cellular and Molecular …, 2014 - Elsevier
Cardiomyopathies are a heterogeneous group of disorders characterized by myocardial
dysfunction that variably progress to a range of clinical symptoms including congestive heart …

[PDF][PDF] Fibrillin-1, function and dysfunction in myocardial tissue: observations in Marfan syndrome

F Steijns - 2020 - biblio.ugent.be
The information in this document is confidential to the person to whom it is addressed and
should not be disclosed to any other person. It may not be reproduced in whole, or in part …

Cardiomiopatia hipertrófica associada a ventrículo esquerdo não compactado: um relato de caso

LSC Mroginski, R Scalabrin… - Research, Society and …, 2021 - rsdjournal.org
Objective: Report the concomitance of two cardiomyopathies: Hypertrophic cardiomyopathy
and Left ventricular noncompaction on a 27 years old patient. Method: Literature research …

The cardiomyopathies

FL Lorini, A Rizza, F Ferri - Textbook of Echocardiography for Intensivists …, 2019 - Springer
The cardiomyopathies are a heterogeneous group of disease of the myocardium.
Historically in the WHO/International Society and Federation of Cardiology classification of …