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Mitochondrial cardiomyopathies [PDF]
Frontiers 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
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Sex‐Related Differences in Genetic Cardiomyopathies
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2022 Cardiomyopathies are a heterogeneous collection of diseases that have in common primary functional and structural abnormalities of the heart muscle, often genetically determined.
Alessia Argirò +8 more
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Myocardial Inflammation as a Manifestation of Genetic Cardiomyopathies: From Bedside to the Bench
Biomolecules, 2023 Over recent years, preclinical and clinical evidence has implicated myocardial inflammation (M-Infl) in the pathophysiology and phenotypes of traditionally genetic cardiomyopathies. M-Infl resembling myocarditis on imaging and histology occurs frequently
Giovanni Peretto +8 more
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Overview of Cardiomyopathies in Childhood
Frontiers 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
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Cardiac Magnetic Resonance Imaging in the Evaluation and Prognosis of Infiltrative Cardiomyopathies [PDF]
Journal of Cardiovascular Development and DiseaseAdvancements in cardiac magnetic resonance (CMR) imaging quality and availability have made it an essential tool in the care of individuals living with cardiomyopathies.
Merna Hussien +5 more
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Survival of patients with cardiomyopathies [PDF]
Българска 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
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Diagnostic and prognostic role of late gadolinium enhancement in cardiomyopathies
European Heart Journal, Supplement, 2023 Late gadolinium enhancement (LGE) is the most relevant tool of cardiac magnetic resonance for tissue characterization, and it plays a pivotal role for diagnostic and prognostic assessment of cardiomyopathies.
G. Aquaro +6 more
semanticscholar +1 more source
Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies
Science, 2022 Pathogenic variants in genes that cause dilated cardiomyopathy (DCM) and arrhythmogenic cardiomyopathy (ACM) convey high risks for the development of heart failure through unknown mechanisms.
D. Reichart +53 more
semanticscholar +1 more source
Non Coding RNAs as Regulators of Wnt/β-Catenin and Hippo Pathways in Arrhythmogenic Cardiomyopathy
Biomedicines, 2022 Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiomyopathy histologically characterized by the replacement of myocardium by fibrofatty infiltration, cardiomyocyte loss, and inflammation.
Marina Piquer-Gil +5 more
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Re-Definition of the Epidemiology of Cardiac Amyloidosis
Biomedicines, 2022 The epidemiology of cardiac amyloidosis (CA), traditionally considered a rare and incurable disease, has changed drastically over the last ten years, particularly due to the advances in diagnostic methods and therapeutic options in the field of ...
Maddalena Rossi +9 more
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