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Arrhythmogenic Cardiomyopathy. [PDF]
Circulation Research, 2021 Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to sudden cardiac death, particularly in young patients and athletes.
D. Corrado, C. Basso, D. Judge
semanticscholar +4 more sources
Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy
New England Journal of Medicine, 2018 Background Transthyretin amyloid cardiomyopathy is caused by the deposition of transthyretin amyloid fibrils in the myocardium. The deposition occurs when wild‐type or variant transthyretin becomes unstable and misfolds. Tafamidis binds to transthyretin,
Mathew S Maurer +2 more
exaly +2 more sources
Nature Reviews Disease Primers, 2019 Dilated cardiomyopathy (DCM) is a clinical diagnosis characterized by left ventricular or biventricular dilation and impaired contraction that is not explained by abnormal loading conditions (for example, hypertension and valvular heart disease) or ...
H. Schultheiss +10 more
semanticscholar +6 more sources
Cardiomyopathy in obesity, insulin resistance and diabetes
Journal of Physiology, 2020 The prevalence of obesity, insulin resistance and diabetes is increasing rapidly. Most patients with these disorders have hypertriglyceridaemia and increased plasma levels of fatty acids, which are taken up and stored in lipid droplets in the heart ...
Junichi Sadoshima, Michinari Nakamura
exaly +2 more sources
Characteristics and Outcomes of Elderly Patients With Hypertrophic Cardiomyopathy
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2021 Background We report characteristics and outcomes of elderly patients with hypertrophic cardiomyopathy (HCM) with basal septal hypertrophy and dynamic left ventricular outflow tract obstruction.
Alaa Alashi +8 more
doaj +1 more source
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2021 Background Hypertrophic cardiomyopathy (HCM) and aortic stenosis can cause obstruction to the flow of blood out of the left ventricular outflow tract into the aorta, with obstructive HCM resulting in dynamic left ventricular outflow tract obstruction and
Milind Y. Desai +9 more
doaj +1 more source
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2021 Background In patients with obstructive hypertrophic cardiomyopathy, surgical myectomy (SM) is indicated for severe symptoms. We sought to compare long‐term outcomes of patients with obstructive hypertrophic cardiomyopathy where SM was based on guideline‐
Alaa Alashi +7 more
doaj +1 more source
Expanding the deep-learning model to diagnosis LVNC: Limitations and trade-offs [PDF]
Computer Methods in Biomechanics and Biomedical Engineering:
Imaging & Visualization. 2024, 2023 Hyper-trabeculation or non-compaction in the left ventricle of the myocardium (LVNC) is a recently classified form of cardiomyopathy. Several methods have been proposed to quantify the trabeculae accurately in the left ventricle, but there is no general agreement in the medical community to use a particular approach.
arxiv +1 more source
Takotsubo is not a cardiomyopathy [PDF]
International Journal of Cardiology, 2018 Unraveling the mechanisms underlying Takotsubo (TTS) leads to question the current inclusion of the condition within the spectrum of cardiomyopathies. Indeed, the clinical presentation and pathophysiology of TTS clearly differ from cardiomyopathies, i.e.
Francesco Pelliccia +5 more
openaire +9 more sources