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Journal of the American College of Cardiology
|
April 20, 2004
Short QT syndrome: pharmacological treatment
Fiorenzo Gaita, Carla Giustetto, Francesca Bianchi, et al.
Global Cardiology Science & Practice
|
October 3, 2022
Evaluation of a novel rapid genomic test including polygenic risk scores for the diagnosis and management of familial hypercholesterolaemia
Emma Neves, Tina Khan, Maggie Williams, et al.
Journal of Cardiac Failure
|
December 16, 2014
A novel mutation in lamin a/c causing familial dilated cardiomyopathy associated with sudden cardiac death
Alexandra Pérez-Serra, Rocío Toro, Oscar Campuzano, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society
|
March 18, 2017
Short QT syndrome in pediatrics
Roberta Pereira, Oscar Campuzano, Georgia Sarquella-Brugada, et al.
International Journal of Legal Medicine
|
June 7, 2024
Investigating cardiac genetic background in sudden infant death syndrome (SIDS)
Francesca Cazzato, Mònica Coll, Simone Grassi, et al.
Heart (British Cardiac Society)
|
June 23, 2011
Meta-analyses of the association between cytochrome CYP2C19 loss- and gain-of-function polymorphisms and cardiovascular outcomes in patients with coronary artery disease treated with clopidogrel
Michel Zabalza, Isaac Subirana, Joan Sala, et al.
Journal of Cardiovascular Electrophysiology
|
July 14, 2006
Familial pseudo-Wolff-Parkinson-White syndrome
Eduardo Back Sternick, Antonio Oliva, Luiz P Magalhães, et al.
Cardiology
|
November 1, 2007
Clinical heterogeneity in sodium channelopathies. What is the meaning of carrying a genetic mutation?
Antonio Oliva, Preben Bjerregaard, Kui Hong, et al.
The American Journal of Case Reports
|
July 11, 2017
Wolff-Parkinson-White Syndrome with Ventricular Hypertrophy in a Brazilian Family
Lenises de Paula van der Steld, Oscar Campuzano, Alexandra Pérez-Serra, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society
|
November 16, 2014
Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy
Mireia Alcalde, Oscar Campuzano, Georgia Sarquella-Brugada, et al.
Page
of 34
Search research articles
Search
Showing results (131-140 of 332) with videos related to
Sort By:
Page
of 34
Journal of the American College of Cardiology
|
April 20, 2004
Short QT syndrome: pharmacological treatment
Fiorenzo Gaita, Carla Giustetto, Francesca Bianchi, et al.
Global Cardiology Science & Practice
|
October 3, 2022
Evaluation of a novel rapid genomic test including polygenic risk scores for the diagnosis and management of familial hypercholesterolaemia
Emma Neves, Tina Khan, Maggie Williams, et al.
Journal of Cardiac Failure
|
December 16, 2014
A novel mutation in lamin a/c causing familial dilated cardiomyopathy associated with sudden cardiac death
Alexandra Pérez-Serra, Rocío Toro, Oscar Campuzano, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society
|
March 18, 2017
Short QT syndrome in pediatrics
Roberta Pereira, Oscar Campuzano, Georgia Sarquella-Brugada, et al.
International Journal of Legal Medicine
|
June 7, 2024
Investigating cardiac genetic background in sudden infant death syndrome (SIDS)
Francesca Cazzato, Mònica Coll, Simone Grassi, et al.
Heart (British Cardiac Society)
|
June 23, 2011
Meta-analyses of the association between cytochrome CYP2C19 loss- and gain-of-function polymorphisms and cardiovascular outcomes in patients with coronary artery disease treated with clopidogrel
Michel Zabalza, Isaac Subirana, Joan Sala, et al.
Journal of Cardiovascular Electrophysiology
|
July 14, 2006
Familial pseudo-Wolff-Parkinson-White syndrome
Eduardo Back Sternick, Antonio Oliva, Luiz P Magalhães, et al.
Cardiology
|
November 1, 2007
Clinical heterogeneity in sodium channelopathies. What is the meaning of carrying a genetic mutation?
Antonio Oliva, Preben Bjerregaard, Kui Hong, et al.
The American Journal of Case Reports
|
July 11, 2017
Wolff-Parkinson-White Syndrome with Ventricular Hypertrophy in a Brazilian Family
Lenises de Paula van der Steld, Oscar Campuzano, Alexandra Pérez-Serra, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society
|
November 16, 2014
Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy
Mireia Alcalde, Oscar Campuzano, Georgia Sarquella-Brugada, et al.
Page
of 34