Results 21 to 30 of about 3,052,792 (294)

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, Elena Arbelo, Elena Arbelo, Elena Arbelo, Elena Arbelo, Estefanía Martínez-Barrios, Patricia Cerralbo, Sergi Cesar, José Cruzalegui, Freddy Chipa, Victoria Fiol, Irene Zschaeck, Clara Hernández, Oscar Campuzano, Oscar Campuzano, Oscar Campuzano, Georgia Sarquella-Brugada, Georgia Sarquella-Brugada, Georgia Sarquella-Brugada   +18 more
doaj   +1 more source

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

Fayixue 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   +1 more source

Sudden Cardiac Death [PDF]

Circulation, 1998
Sudden cardiac death describes the unexpected natural death from a cardiac cause within a short time period, generally ≤ 1 h from the onset of symptoms, in a person without any prior condition that would appear fatal [1, 2]. Such a rapid death is often attributed to a cardiac arrhythmia, but with the advent of monitoring capabilities from implantable ...
D P, Zipes, H J, Wellens
openaire   +2 more sources

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

Frontiers 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, Elena Arbelo, Elena Arbelo, Elena Arbelo, Sergi Cesar, José Cruzalegui, Victoria Fiol, Nuria Díez-Escuté, Clara Hernández, Ramon Brugada, Ramon Brugada, Ramon Brugada, Ramon Brugada, Josep Brugada, Josep Brugada, Josep Brugada, Josep Brugada, Oscar Campuzano, Oscar Campuzano, Oscar Campuzano, Georgia Sarquella-Brugada, Georgia Sarquella-Brugada   +21 more
doaj   +1 more source

Inherited Arrhythmogenic Syndromes

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

Genetics of Heritable Thoracic Aortic Disease

Cardiogenetics, 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, Dimitrios Degiannis, Aris Anastasakis   +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

Annals 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, Borje Darpo, Randy Brown, Todd Rudo, Svetlana Chamoun, David E. Albert, Johan Martijn Bos, Michael J. Ackerman   +7 more
doaj   +1 more source

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

Scientific 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, J. Martijn Bos, Surendra Dasari, Kenneth L. Johnson, David J. Tester, John R. Giudicessi, Cristobal dos Remedios, Joseph J. Maleszewski, Steve R. Ommen, Joseph A. Dearani, Michael J. Ackerman   +10 more
doaj   +1 more source

Aetiology of sudden cardiac death in sport: a histopathologist's perspective. [PDF]

, 2012
In the UK, when a young person dies suddenly, the coroner is responsible for establishing the cause of death. They will ask a consultant pathologist to carry out an autopsy in order to ascertain when, where and how that person died.
Sheppard, MN
core   +1 more source

Omega-3 Index and Sudden Cardiac Death [PDF]

, 2010
Sudden cardiac death (SCD) is an unresolved health issue, and responsible for 15% of all deaths in Western countries. Epidemiologic evidence, as well as evidence from clinical trials, indicates that increasing intake and high levels of eicosapentaenoic ...
Schacky, Clemens von, Von Schacky
core   +1 more source