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Guido D Pollevick

Showing results (11-20 of 23) with videos related to

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Circulation. Cardiovascular Genetics|December 25, 2009
A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotypeDan Hu, Hector Barajas-Martinez, Elena Burashnikov, et al.
Heart Rhythm|August 7, 2007
Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarctionDan Hu, Sami Viskin, Antonio Oliva, et al.
Heart Rhythm|February 18, 2012
Torsades de pointes following acute myocardial infarction: evidence for a deadly link with a common genetic variantLia Crotti, Dan Hu, Hector Barajas-Martinez, et al.
Circulation|November 3, 2004
Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutationsKui Hong, Josep Brugada, Antonio Oliva, et al.
Circulation. Arrhythmia and Electrophysiology|January 6, 2009
Functional effects of KCNE3 mutation and its role in the development of Brugada syndromeEva Delpón, Jonathan M Cordeiro, Lucía Núñez, et al.
Heart Rhythm|March 4, 2008
Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillationLasse S Ravn, Yoshiyasu Aizawa, Guido D Pollevick, et al.
Circulation|December 17, 2003
Sudden death associated with short-QT syndrome linked to mutations in HERGRamon Brugada, Kui Hong, Robert Dumaine, et al.
Heart Rhythm|September 7, 2010
Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac deathElena Burashnikov, Ryan Pfeiffer, Héctor Barajas-Martinez, et al.
Circulation|January 17, 2007
Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac deathCharles Antzelevitch, Guido D Pollevick, Jonathan M Cordeiro, et al.
Journal of the American College of Cardiology|June 4, 2011
Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noiseJamie D Kapplinger, Andrew P Landstrom, Benjamin A Salisbury, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Circulation. Cardiovascular Genetics|December 25, 2009
A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotypeDan Hu, Hector Barajas-Martinez, Elena Burashnikov, et al.
Heart Rhythm|August 7, 2007
Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarctionDan Hu, Sami Viskin, Antonio Oliva, et al.
Heart Rhythm|February 18, 2012
Torsades de pointes following acute myocardial infarction: evidence for a deadly link with a common genetic variantLia Crotti, Dan Hu, Hector Barajas-Martinez, et al.
Circulation|November 3, 2004
Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutationsKui Hong, Josep Brugada, Antonio Oliva, et al.
Circulation. Arrhythmia and Electrophysiology|January 6, 2009
Functional effects of KCNE3 mutation and its role in the development of Brugada syndromeEva Delpón, Jonathan M Cordeiro, Lucía Núñez, et al.
Heart Rhythm|March 4, 2008
Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillationLasse S Ravn, Yoshiyasu Aizawa, Guido D Pollevick, et al.
Circulation|December 17, 2003
Sudden death associated with short-QT syndrome linked to mutations in HERGRamon Brugada, Kui Hong, Robert Dumaine, et al.
Heart Rhythm|September 7, 2010
Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac deathElena Burashnikov, Ryan Pfeiffer, Héctor Barajas-Martinez, et al.
Circulation|January 17, 2007
Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac deathCharles Antzelevitch, Guido D Pollevick, Jonathan M Cordeiro, et al.
Journal of the American College of Cardiology|June 4, 2011
Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noiseJamie D Kapplinger, Andrew P Landstrom, Benjamin A Salisbury, et al.
Pageof 3