Results 81 to 90 of about 445,510 (263)

Hereditary dilated cardiomyopathy

open access: yesClinical Cardiology, 1995
AbstractDilated cardiomyopathy (DCM) is a common and important cause of morbidity and mortality. Many factors can contribute to the development of this disorder, although most commonly the etiology is unexplained. However, recent studies in individuals with idiopathic DCM now reveal a heritable cause in 20–30% of individuals.
John Ross, Thomas R. Mcminn
openaire   +3 more sources

Taurine deficiency and dilated cardiomyopathy in golden retrievers fed commercial diets

open access: yesPLoS ONE, 2018
Introduction Golden retrievers are over-represented in cases of taurine-deficient dilated cardiomyopathy and recently a surge in cases has prompted further investigation.
J. Kaplan   +22 more
semanticscholar   +1 more source

Left Ventricular Unloading in Nonischemic Dilated Cardiomyopathy Improves Coronary Haemodynamic Reserve

open access: yesCatheterization and Cardiovascular Interventions, EarlyView.
ABSTRACT Background The Impella CP is a catheter‐based ventricular assist device used in the management of cardiogenic shock and to support high‐risk percutaneous coronary interventions (PCI). Despite its growing use, the effects of Impella CP on coronary flow dynamics as measured by intracoronary continuous thermodilution have not been fully ...
Samer Fawaz   +9 more
wiley   +1 more source

Automatic Segmentation and Disease Classification Using Cardiac Cine MR Images [PDF]

open access: yesarXiv, 2017
Segmentation of the heart in cardiac cine MR is clinically used to quantify cardiac function. We propose a fully automatic method for segmentation and disease classification using cardiac cine MR images. A convolutional neural network (CNN) was designed to simultaneously segment the left ventricle (LV), right ventricle (RV) and myocardium in end ...
arxiv  

Comparison of long‐term outcome in anthracycline‐related versus idiopathic dilated cardiomyopathy: a single centre experience

open access: yesEuropean Journal of Heart Failure, 2018
Cardiac dysfunction is a severe complication of anthracycline‐containing anticancer therapy. The outcome of anthracycline‐induced cardiomyopathy (AICM) compared with other non‐ischaemic causes of heart failure (HF), such as idiopathic dilated ...
A. Fornaro   +12 more
semanticscholar   +1 more source

Dilated cardiomyopathy due to hypocalcaemia: a case report

open access: yesJournal of Medical Case Reports
Background Hypocalcaemia is a rare, but reversible, cause of dilated cardiomyopathy causing heart failure. Several case reports have been reported on reversible cardiomyopathy secondary to hypocalcaemia.
Nilushka Rupasinghe   +2 more
doaj   +1 more source

Molecular studies in familial dilated cardiomyopathy – A pilot study

open access: yesInternational Journal of Cardiology: Heart & Vasculature, 2022
Aim: To study genetic variants in patients of familial dilated cardiomyopathy. Methodology: Patients with reduced ejection fraction of less than 45% and dilated left ventricle are considered to have dilated cardiomyopathy.
Vyom Mori   +11 more
doaj  

Deep learning approach to left ventricular non-compaction measurement [PDF]

open access: yesarXiv, 2020
Left ventricular non-compaction (LVNC) is a rare cardiomyopathy characterized by abnormal trabeculations in the left ventricle cavity. Although traditional computer vision approaches exist for LVNC diagnosis, deep learning-based tools could not be found in the literature.
arxiv  

Association Between Midwall Late Gadolinium Enhancement and Sudden Cardiac Death in Patients With Dilated Cardiomyopathy and Mild and Moderate Left Ventricular Systolic Dysfunction

open access: yesCirculation, 2017
Background: Current guidelines only recommend the use of an implantable cardioverter defibrillator in patients with dilated cardiomyopathy for the primary prevention of sudden cardiac death (SCD) in those with a left ventricular ejection fraction (LVEF ...
B. Halliday   +24 more
semanticscholar   +1 more source

Knockout of rbm24a and rbm24b genes in zebrafish impairs skeletal and cardiac muscle integrity and function during development

open access: yesDevelopmental Dynamics, EarlyView.
Abstract Backgound Skeletal and cardiac muscles are contractile tissues whose development and function are dependent on genetic programs that must be precisely orchestrated in time and space. In addition to transcription factors, RNA‐binding proteins tightly regulate gene expression by controlling the fate of RNA transcripts, thus specific proteins ...
Audrey Saquet   +3 more
wiley   +1 more source

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