Results 1 to 10 of about 605,333 (128)
Cardiovascular Pathology, 2000 The rate of cardiac deaths that are sudden is approximately 50%, and decreases with age. The causes of sudden cardiac death are diverse, and are a function of age. In children and adolescents, coronary anomalies, hypertrophic cardiomyopathy and myocarditis are frequent substrates for lethal arrhythmias; in adults, coronary atherosclerosis and acquired ...
Bayés de Luna, Antoni +3 more
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Forensic Sciences Research, 2019 Cardiovascular disease represents the main cause of death in developed countries. Cardiovascular disease frequently may account for premature fatal outcomes, even in the apparently healthy young, a...
Joaquín S. Lucena
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EDIS, 2004 Sudden oak death is a new disease capable of causing a range of symptoms from leaf spots to plant death on many woody hosts. Because sudden oak death is a new disease, much about the pathogen, host range, and the disease epidemiology is unknown.
Philip F. Harmon, Carrie L. Harmon
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Journal of the Practice of Cardiovascular Sciences, 2015 Sudden cardiac death is one of the most common cause of mortality worldwide. Despite significant advances in the medical science, there is little improvement in the sudden cardiac death related mortality.
Neeraj Parakh
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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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Advanced Genetics, 2023 In sudden unexplained death in pediatrics (SUDP) the cause of death is unknown despite an autopsy and investigation. The role of copy number variations (CNVs) in SUDP has not been well‐studied. Chromosomal microarray (CMA) data are generated for 116 SUDP
Catherine A. Brownstein +14 more
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Journal of Cardiovascular Development and Disease, 2022 We report a pediatric patient with persistent left superior vena cava and a D-transposition of great arteries, which is an uncommon relation. It is crucial to know the anatomy of the persistent left superior vena cava and the dilated coronary sinus to ...
José Cruzalegui +5 more
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Sex differences in long QT syndrome
Frontiers in Cardiovascular Medicine, 2023 Long QT Syndrome (LQTS) is a rare, inherited channelopathy characterized by cardiac repolarization dysfunction, leading to a prolonged rate-corrected QT interval in patients who are at risk for malignant ventricular tachyarrhythmias, syncope, and even ...
Nuria Díez-Escuté +18 more
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Val50Met hereditary transthyretin amyloidosis: not just a medical problem, but a psychosocial burden
Orphanet Journal of Rare Diseases, 2021 Background Hereditary transthyretin (TTR) amyloidosis (ATTRv) is a heterogeneous disease with a clinical presentation that varies according to geographical area and TTR mutation.
Juan González-Moreno +11 more
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Structural imaging biomarkers of sudden unexpected death in epilepsy. [PDF]
, 2015 Sudden unexpected death in epilepsy is a major cause of premature death in people with epilepsy. We aimed to assess whether structural changes potentially attributable to sudden death pathogenesis were present on magnetic resonance imaging in people who ...
Balestrini, Simona +12 more
core +3 more sources