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Ramon Brugada

Showing results (251-260 of 287) with videos related to

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Cerebral Cortex (New York, N.Y. : 1991)|March 21, 2022
The effect of external stimulation on functional networks in the aging healthy human brainAnira Escrichs, Yonatan Sanz Perl, Noelia Martínez-Molina, et al.
European Journal of Heart Failure|May 25, 2026
Genetic Determinants of Severity and Recurrence in Arrhytmia-Induced CardiomyopathyColoma Tiron, Marc Soriano-Amores, Raúl Ramos-Polo, et al.
International Journal of Molecular Sciences|September 27, 2025
Global and Sex-Stratified Genome-Wide Association Study of Long COVID Based on Patient-Driven Symptom RecallSara Polo-Alonso, Álvaro Hernáez, Irene R Dégano, 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.
Circulation|November 14, 2007
Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel functionStephan E Lehnart, Michael J Ackerman, D Woodrow Benson, et al.
Pageof 29

Showing results (251-260 of 287) with videos related to

Sort By:
Pageof 29
Cerebral Cortex (New York, N.Y. : 1991)|March 21, 2022
The effect of external stimulation on functional networks in the aging healthy human brainAnira Escrichs, Yonatan Sanz Perl, Noelia Martínez-Molina, et al.
European Journal of Heart Failure|May 25, 2026
Genetic Determinants of Severity and Recurrence in Arrhytmia-Induced CardiomyopathyColoma Tiron, Marc Soriano-Amores, Raúl Ramos-Polo, et al.
International Journal of Molecular Sciences|September 27, 2025
Global and Sex-Stratified Genome-Wide Association Study of Long COVID Based on Patient-Driven Symptom RecallSara Polo-Alonso, Álvaro Hernáez, Irene R Dégano, 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.
Circulation|November 14, 2007
Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel functionStephan E Lehnart, Michael J Ackerman, D Woodrow Benson, et al.
Pageof 29