Results 11 to 20 of about 44,322 (189)

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   +4 more sources

Cardiomyopathies: Temporal Review and Genetic Determination [PDF]

open access: yesBiomedicines
Cardiomyopathies are a heterogeneous group of diseases of the myocardium associated with dysfunction, with or without a structural substrate. They are frequently genetically determined. The dysfunction may be mechanical, both of the systole and diastole,
Gaetano Thiene   +2 more
doaj   +3 more sources

Survival of patients with cardiomyopathies [PDF]

open access: yesБългарска кардиология, 2021
Cardiomyopathies are a heterogeneous group of diseases. The main pathogenetic mechanism is myocardial damage due to genetic mutations. Cardiomyopathies are one of the leading causes of heart failure, sudden cardiac death, and life-threatening arrhythmias.
Monika Shumkova   +4 more
doaj   +4 more sources

Infiltrative Cardiomyopathies

open access: yesClinical Medicine Insights: Cardiology, 2015
Infiltrative cardiomyopathies can result from a wide spectrum of both inherited and acquired conditions with varying systemic manifestations. They portend an adverse prognosis, with only a few exceptions (ie, glycogen storage disease), where early ...
David Bejar   +3 more
doaj   +3 more sources

Overview of Cardiomyopathies in Childhood

open access: yesFrontiers in Pediatrics, 2021
Paediatric cardiomyopathies are a heterogenous group of rare disorders, characterised by mechanical and electrical abnormalities of the heart muscle. The overall annual incidence of childhood cardiomyopathies is estimated at about 1 per 100,000 children ...
Anika Rath   +3 more
doaj   +3 more sources

ICD Outcome in Pediatric Cardiomyopathies

open access: yesJournal of Cardiovascular Development and Disease, 2022
Background: Pediatric patients with cardiomyopathies are at risk of malignant arrhythmias and sudden cardiac death (SCD). An ICD may prevent SCD. The aim of this study was to evaluate ICD implantation outcomes, and to compare transvenous and subcutaneous
Massimo Stefano Silvetti   +10 more
doaj   +2 more sources

Clinical genetic aspects of cardiomyopathies

open access: yesJournal of the Practice of Cardiovascular Sciences, 2015
Cardiomyopathies are a major cause of heart disease. Not only the patients, but also their families are severely burdened by these illnesses. In the past decade, studies revealed the heterogeneity of these diseases in terms of clinical presentation, as ...
Mitali Kapoor   +2 more
doaj   +2 more sources

Inherited Cardiomyopathies: Genetics and Clinical Genetic Testing

open access: yesCardiovascular Innovations and Applications, 2017
Inherited cardiomyopathies are major causes of morbidity and mortality and include a group of cardiac disorders such as hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy, arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C), left ...
Guoliang Wang   +4 more
doaj   +3 more sources

Role of cardiac MRI in nonischemic cardiomyopathies

open access: yesIndian Heart Journal, 2016
Cardiac magnetic resonance (CMR) with its higher spatial resolution is considered the gold standard for evaluating ventricular mass, volumes, and ejection fraction. CMR can be used for accurate diagnosis of several conditions, especially cardiomyopathies.
Senthil Anand, Rajesh Janardhanan
doaj   +2 more sources

Reversible Cardiomyopathies

open access: yesClinical Medicine Insights: Cardiology, 2015
Cardiomyopathies (CMs) have many etiological factors that can result in severe structural and functional dysregulation. Fortunately, there are several potentially reversible CMs that are known to improve when the root etiological factor is addressed.
Harsh Patel   +4 more
doaj   +3 more sources

Home - About - Disclaimer - Privacy