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Ramon Brugada

Showing results (121-130 of 332) with videos related to

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Revista Espanola De Cardiologia (English Ed.)|October 6, 2018
Characterization of electrocardiographic findings in young studentsPau Vilardell, Josep Brugada, Jaime Aboal, et al.
Plos One|July 9, 2016
Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 GeneRocio Toro, Alexandra Pérez-Serra, Oscar Campuzano, et al.
American Journal of Physiology. Heart and Circulatory Physiology|April 2, 2013
DiBAC₄(3) hits a "sweet spot" for the activation of arterial large-conductance Ca²⁺-activated potassium channels independently of the β₁-subunitFabiana S Scornik, Ronald S Bucciero, Yuesheng Wu, et al.
Heart Failure Clinics|March 30, 2010
Genetic basis of ventricular arrhythmiasTim Boussy, Gaetano Paparella, Carlo de Asmundis, et al.
Heart Rhythm|November 26, 2023
Loss of sodium current caused by a Brugada syndrome-associated variant is determined by patient-specific genetic backgroundRebecca Martínez-Moreno, David Carreras, Georgia Sarquella-Brugada, et al.
European Heart Journal|March 18, 2010
Number of electrocardiogram leads displaying the diagnostic coved-type pattern in Brugada syndrome: a diagnostic consensus criterion to be revisedSergio Richter, Andrea Sarkozy, Gaetano Paparella, et al.
Pacing and Clinical Electrophysiology : PACE|August 30, 2007
Shocking truths about implantable cardioverter defibrillator monitoring zonesFadi Mansour, Bernard Thibault, Marc Dubuc, et al.
Pacing and Clinical Electrophysiology : PACE|September 2, 2009
A nonsense SCN5A mutation associated with Brugada-type electrocardiogram and intraventricular conduction defectsKaveh Samani, Tomohiko Ai, Jeffrey A Towbin, et al.
Heartrhythm Case Reports|May 12, 2017
Short QT and atrial fibrillation: A <i>KCNQ1</i> mutation-specific disease. Late follow-up in three unrelated childrenGeorgia Sarquella-Brugada, Oscar Campuzano, Anna Iglesias, et al.
Journal of Clinical Medicine|June 19, 2020
Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic InterpretationOscar Campuzano, Georgia Sarquella-Brugada, Elena Arbelo, et al.
Pageof 34

Showing results (121-130 of 332) with videos related to

Sort By:
Pageof 34
Revista Espanola De Cardiologia (English Ed.)|October 6, 2018
Characterization of electrocardiographic findings in young studentsPau Vilardell, Josep Brugada, Jaime Aboal, et al.
Plos One|July 9, 2016
Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 GeneRocio Toro, Alexandra Pérez-Serra, Oscar Campuzano, et al.
American Journal of Physiology. Heart and Circulatory Physiology|April 2, 2013
DiBAC₄(3) hits a "sweet spot" for the activation of arterial large-conductance Ca²⁺-activated potassium channels independently of the β₁-subunitFabiana S Scornik, Ronald S Bucciero, Yuesheng Wu, et al.
Heart Failure Clinics|March 30, 2010
Genetic basis of ventricular arrhythmiasTim Boussy, Gaetano Paparella, Carlo de Asmundis, et al.
Heart Rhythm|November 26, 2023
Loss of sodium current caused by a Brugada syndrome-associated variant is determined by patient-specific genetic backgroundRebecca Martínez-Moreno, David Carreras, Georgia Sarquella-Brugada, et al.
European Heart Journal|March 18, 2010
Number of electrocardiogram leads displaying the diagnostic coved-type pattern in Brugada syndrome: a diagnostic consensus criterion to be revisedSergio Richter, Andrea Sarkozy, Gaetano Paparella, et al.
Pacing and Clinical Electrophysiology : PACE|August 30, 2007
Shocking truths about implantable cardioverter defibrillator monitoring zonesFadi Mansour, Bernard Thibault, Marc Dubuc, et al.
Pacing and Clinical Electrophysiology : PACE|September 2, 2009
A nonsense SCN5A mutation associated with Brugada-type electrocardiogram and intraventricular conduction defectsKaveh Samani, Tomohiko Ai, Jeffrey A Towbin, et al.
Heartrhythm Case Reports|May 12, 2017
Short QT and atrial fibrillation: A <i>KCNQ1</i> mutation-specific disease. Late follow-up in three unrelated childrenGeorgia Sarquella-Brugada, Oscar Campuzano, Anna Iglesias, et al.
Journal of Clinical Medicine|June 19, 2020
Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic InterpretationOscar Campuzano, Georgia Sarquella-Brugada, Elena Arbelo, et al.
Pageof 34