Results 11 to 20 of about 38,525 (259)

Mitochondrial cardiomyopathies [PDF]

open access: yesFrontiers in Cardiovascular Medicine, 2016
Mitochondria are found in all nucleated human cells and perform a variety of essential functions, including the generation of cellular energy. Mitochondria are under dual genome control.
Ayman W. El-Hattab, Fernando Scaglia
doaj   +3 more sources

Atrial Cardiomyopathy

open access: yesESC Heart Failure
ESC Heart Failure, Volume 12, Issue 2, Page 727-729, April 2025.
Wojciech Kosmala   +1 more
openaire   +4 more sources

Stress Cardiomyopathy (Takotsubo Cardiomyopathy) [PDF]

open access: yesClinical medicine. Cardiology, 2009
Background Due to the rise in the number of reports of stress cardiomyopathy in the literature, awareness of this condition is increasing. Although different names have been used to describe this condition, the similarities in clinical, electrocardiographic, echocardiographic and angiographic features suggest ...
Samer Khouri, Naser Imran
openaire   +3 more sources

Cardiomyopathies

open access: yesJournal de Radiologie, 2004
Cardiomyopathies include a wide variety of cardiac diseases. The value of MR imaging is not only to provide information about cardiac function, but also to detect the underlying cause of the disease.
J P, Laissy   +3 more
openaire   +4 more sources

Cardiomyopathies.

open access: yesActa bio-medica : Atenei Parmensis, 2019
The most common cardiomyopathies often present to primary care physicians with similar symptoms, despite the fact that they involve a variety of phenotypes and etiologies (1). Many have signs and symptoms common in heart failure, such as reduced ejection fraction, peripheral edema, fatigue, orthopnea, exertion dyspnea, paroxysmal nocturnal dyspnea ...
Precone, Vincenza   +9 more
openaire   +2 more sources

Cardiomyopathies in China: A 2018–2019 state-of-the-art review

open access: yesChronic Diseases and Translational Medicine, 2020
Cardiomyopathies are diseases of the cardiac muscle and are often characterized by ventricular dilation, hypertrophy, and cardiac arrhythmia. Patients with cardiomyopathies often experience sudden death and cardiac failure and require cardiac ...
Tian-Rui Hua, Shu-Yang Zhang
doaj   +1 more source

Arrhythmogenic Cardiomyopathy [PDF]

open access: yesCirculation Research, 2017
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to sudden cardiac death, particularly in young patients and athletes. Pathological features include loss of myocytes and fibrofatty replacement of right ventricular myocardium; biventricular involvement is often observed.
Corrado, Domenico   +2 more
openaire   +3 more sources

Targeting lipid metabolism as a new therapeutic strategy for inherited cardiomyopathies

open access: yesFrontiers in Cardiovascular Medicine, 2023
Inherited cardiomyopathies caused by pathological genetic variants include multiple subtypes of heart disease. Advances in next-generation sequencing (NGS) techniques have allowed for the identification of numerous genetic variants as pathological ...
Karen R. Gaar-Humphreys   +16 more
doaj   +1 more source

Transcriptome data analysis of primary cardiomyopathies reveals perturbations in arachidonic acid metabolism

open access: yesFrontiers in Cardiovascular Medicine, 2023
IntroductionCardiomyopathies are complex heart diseases with significant prevalence around the world. Among these, primary forms are the major contributors to heart failure and sudden cardiac death.
Pankaj Kumar Chauhan   +3 more
doaj   +1 more source

Dilated cardiomyopathies and non-compaction cardiomyopathy [PDF]

open access: yesHerz, 2020
AbstractDilated cardiomyopathy (DCM) is the most common form of cardiomyopathy and one of the most common causes of heart failure. It is characterized by left or biventricular dilation and a reduced systolic function. The causes are manifold and range from myocarditis to alcohol and other toxins, to rheumatological, endocrinological, and metabolic ...
Hänselmann, A.   +3 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy