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Application Prospects and Prospect of Metabolomics in the Identification of Sudden Cardiac Death [PDF]

open access: yesFayixue Zazhi, 2021
In cases of sudden death, the prevention of sudden cardiac death and the analysis of the cause of death after sudden cardiac death have always been a difficult problem.
GU Zhen, NIU Jia-jia, AN Guo-shuai, et al.
doaj   +3 more sources

Pediatric Left Posteroseptal Accessory Pathway Ablation from Giant Coronary Sinus with Persistent Left Superior Cava

open access: yesJournal 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
doaj   +1 more source

Sex differences in long QT syndrome

open access: yesFrontiers 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
doaj   +1 more source

Brugada Syndrome in Women: What Do We Know After 30 Years?

open access: yesFrontiers in Cardiovascular Medicine, 2022
Brugada syndrome (BrS) was initially described in 1992 by Josep and Pedro Brugada as an arrhythmogenic disease characterized by ST segment elevation in the right precordial leads and increased risk of sudden cardiac death (SCD).
Estefanía Martínez-Barrios   +21 more
doaj   +1 more source

Inherited Arrhythmogenic Syndromes

open access: yesCardiogenetics, 2023
Inherited arrhythmogenic syndromes (IASs) are a heterogeneous group of rare cardiac entities of genetic origin [...]
Georgia Sarquella-Brugada   +1 more
doaj   +1 more source

Genetics of Heritable Thoracic Aortic Disease

open access: yesCardiogenetics, 2022
Genetic testing plays an increasing diagnostic and prognostic role in the management of patients with heritable thoracic aortic disease (HTAD). The identification of a specific variant can establish or confirm the diagnosis of syndromic HTAD, dictate ...
Efstathios Papatheodorou   +2 more
doaj   +1 more source

Comparison of electrocardiograms (ECG) waveforms and centralized ECG measurements between a simple 6‐lead mobile ECG device and a standard 12‐lead ECG

open access: yesAnnals of Noninvasive Electrocardiology, 2021
Background Interval duration measurements (IDMs) were compared between standard 12‐lead electrocardiograms (ECGs) and 6‐lead ECGs recorded with AliveCor's KardiaMobile 6L, a hand‐held mobile device designed for use by patients at home.
Robert Kleiman   +7 more
doaj   +1 more source

Improved Cardiac Arrhythmia Prediction Based on Heart Rate Variability Analysis [PDF]

open access: yes, 2022
Many types of ventricular and atrial cardiac arrhythmias have been discovered in clinical practice in the past 100 years, and these arrhythmias are a major contributor to sudden cardiac death. Ventricular tachycardia, ventricular fibrillation, and paroxysmal atrial fibrillation are the most commonly-occurring and dangerous arrhythmias, therefore early ...
arxiv   +1 more source

Proteomic and phosphoproteomic analyses of myectomy tissue reveals difference between sarcomeric and genotype-negative hypertrophic cardiomyopathy

open access: yesScientific Reports, 2023
Hypertrophic cardiomyopathy (HCM) is a genetically heterogenous condition with about half of cases remaining genetically elusive or non-genetic in origin.
Ramin Garmany   +10 more
doaj   +1 more source

Sudden cardiac death [PDF]

open access: yesSrpski Arhiv za Celokupno Lekarstvo, 2004
Sudden cardiac death in an athlete is rare and tragic event. An athlete's death draws high public attention given that athletes are considered the healthiest category of society.
Aranđelović Aleksandra Č.   +3 more
doaj   +1 more source

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