Results 11 to 20 of about 337,480 (272)

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

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

Sudden Cardiac Death and Myocardial Fibrosis, Determined by Autopsy, in Persons with HIV.

New England Journal of Medicine, 2021
BACKGROUND The incidence of sudden cardiac death and sudden death caused by arrhythmia, as determined by autopsy, in persons with human immunodeficiency virus (HIV) infection has not been clearly established.
Z. Tseng, E. Moffatt, A. Kim, E. Vittinghoff, P. Ursell, A. Connolly, J. Olgin, Joseph K Wong, P. Hsue   +8 more
semanticscholar   +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

Sudden cardiac death in athletes

Trends in Urology & Men s Health, 2020
Exercise is generally a good thing. However, for some it holds hidden danger. The following review discusses the incidence and aetiology of sudden cardiac death (SCD) and measures to reduce the burden of SCD.
N. Mannakkara, Sanjay Sharma
semanticscholar   +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

A Validated Model for Sudden Cardiac Death Risk Prediction in Pediatric Hypertrophic Cardiomyopathy

Circulation, 2020
Supplemental Digital Content is available in the text. Background: Hypertrophic cardiomyopathy is the leading cause of sudden cardiac death (SCD) in children and young adults.
A. Miron, M. Lafreniere-Roula, Chun-Po Steve Fan, K. Armstrong, A. Dragulescu, Tanya Papaz, C. Manlhiot, B. Kaufman, R. Butts, L. Gardin, E. Stephenson, Taylor S. Howard, P. Aziz, S. Balaji, Virginie Beauséjour Ladouceur, L. Benson, S. Colan, J. Godown, H. Henderson, J. Ingles, A. Jeewa, J. Jefferies, A. Lal, J. Mathew, E. Jean-St-Michel, M. Michels, S. Nakano, I. Olivotto, J. Parent, A. Pereira, C. Semsarian, R. Whitehill, S. Wittekind, M. Russell, J. Conway, M. Richmond, C. Villa, R. Weintraub, J. Rossano, P. Kantor, Carolyn Y. Ho, S. Mital   +41 more
semanticscholar   +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