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Current Cardiology Reviews
|
September 14, 2018
Electrocardiographic Assessment and Genetic Analysis in Neonates: a Current Topic of Discussion
Georgia Sarquella-Brugada, Sergi Cesar, Maria Dolores Zambrano, et al.
Epilepsia
|
August 1, 2013
Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death
Sara Partemi, Sandrine Cestèle, Marianna Pezzella, et al.
Journal of the American College of Cardiology
|
October 14, 2017
Patients With Brugada Syndrome and Implanted Cardioverter-Defibrillators: Long-Term Follow-Up
Jaime Hernandez-Ojeda, Elena Arbelo, Roger Borras, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
August 15, 2009
The phenotype and potential origin of nestin+ cardiac myocyte-like cells following infarction
Pauline C Béguin, Viviane El-Helou, John Assimakopoulos, et al.
American Heart Journal
|
March 12, 2011
Increase in sudden death from coronary artery disease in young adults
Dabit Arzamendi, Begoña Benito, Helena Tizon-Marcos, et al.
Journal of Medical Genetics
|
March 8, 2013
Genetics of arrhythmogenic right ventricular cardiomyopathy
Oscar Campuzano, Mireia Alcalde, Catarina Allegue, et al.
Forensic Science International
|
December 19, 2016
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia
Cristina Bosch, Oscar Campuzano, Georgia Sarquella-Brugada, et al.
Journal of Cardiovascular Electrophysiology
|
December 18, 2007
Differences in 12-lead electrocardiogram between symptomatic and asymptomatic Brugada syndrome patients
M Juhani Junttila, Pedro Brugada, Kui Hong, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
December 14, 2021
High-quality RNA improves sensitivity of SARS-CoV-2 detection by colorimetric RT-LAMP
Marta Puigmulé, Mònica Coll, Alexandra Pérez-Serra, et al.
Frontiers in Pediatrics
|
March 11, 2021
Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in <i>TRDN</i>: A Comprehensive Interpretation
Georgia Sarquella-Brugada, Anna Fernandez-Falgueras, Sergi Cesar, et al.
Page
of 34
Search research articles
Search
Showing results (211-220 of 332) with videos related to
Sort By:
Page
of 34
Current Cardiology Reviews
|
September 14, 2018
Electrocardiographic Assessment and Genetic Analysis in Neonates: a Current Topic of Discussion
Georgia Sarquella-Brugada, Sergi Cesar, Maria Dolores Zambrano, et al.
Epilepsia
|
August 1, 2013
Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death
Sara Partemi, Sandrine Cestèle, Marianna Pezzella, et al.
Journal of the American College of Cardiology
|
October 14, 2017
Patients With Brugada Syndrome and Implanted Cardioverter-Defibrillators: Long-Term Follow-Up
Jaime Hernandez-Ojeda, Elena Arbelo, Roger Borras, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
August 15, 2009
The phenotype and potential origin of nestin+ cardiac myocyte-like cells following infarction
Pauline C Béguin, Viviane El-Helou, John Assimakopoulos, et al.
American Heart Journal
|
March 12, 2011
Increase in sudden death from coronary artery disease in young adults
Dabit Arzamendi, Begoña Benito, Helena Tizon-Marcos, et al.
Journal of Medical Genetics
|
March 8, 2013
Genetics of arrhythmogenic right ventricular cardiomyopathy
Oscar Campuzano, Mireia Alcalde, Catarina Allegue, et al.
Forensic Science International
|
December 19, 2016
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia
Cristina Bosch, Oscar Campuzano, Georgia Sarquella-Brugada, et al.
Journal of Cardiovascular Electrophysiology
|
December 18, 2007
Differences in 12-lead electrocardiogram between symptomatic and asymptomatic Brugada syndrome patients
M Juhani Junttila, Pedro Brugada, Kui Hong, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
December 14, 2021
High-quality RNA improves sensitivity of SARS-CoV-2 detection by colorimetric RT-LAMP
Marta Puigmulé, Mònica Coll, Alexandra Pérez-Serra, et al.
Frontiers in Pediatrics
|
March 11, 2021
Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in <i>TRDN</i>: A Comprehensive Interpretation
Georgia Sarquella-Brugada, Anna Fernandez-Falgueras, Sergi Cesar, et al.
Page
of 34