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Journal of Personalized Medicine|February 25, 2022
Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic SyndromesEstefanía Martínez-Barrios, Georgia Sarquella-Brugada, Alexandra Pérez-Serra, et al.
Human Genetics|September 21, 2021
Clinical impact of rare variants associated with inherited channelopathies: a 5-year updateGeorgia Sarquella-Brugada, Anna Fernandez-Falgueras, Sergi Cesar, et al.
Plos One|February 7, 2017
Correction: Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic InvestigationOlallo Sanchez, Oscar Campuzano, Anna Fernández-Falgueras, et al.
Journal of Personalized Medicine|March 3, 2021
Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years LaterMarta Vallverdú-Prats, Mireia Alcalde, Georgia Sarquella-Brugada, et al.
International Journal of Legal Medicine|January 24, 2023
Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohortEstefanía Martinez-Barrios, Georgia Sarquella-Brugada, Alexandra Perez-Serra, et al.
Plos One|December 9, 2016
Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic InvestigationOlallo Sanchez, Oscar Campuzano, Anna Fernández-Falgueras, et al.
Forensic Science International. Genetics|April 6, 2020
Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?Jesus Mates, Irene Mademont-Soler, Anna Fernandez-Falgueras, et al.
Frontiers in Genetics|April 10, 2023
LMNA-related muscular dystrophy: Identification of variants in alternative genes and personalized clinical translationSergi Cesar, Monica Coll, Victoria Fiol, et al.
Frontiers in Pediatrics|August 16, 2021
Early Identification of Prolonged QT Interval for Prevention of Sudden Infant DeathGeorgia Sarquella-Brugada, Oscar García-Algar, María Dolores Zambrano, et al.
European Journal of Human Genetics : EJHG|March 8, 2018
Role of copy number variants in sudden cardiac death and related diseases: genetic analysis and translation into clinical practiceJesus Mates, Irene Mademont-Soler, Bernat Del Olmo, et al.
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