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Heart Rhythm
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April 29, 2014
Reply to the Editor--PQ-segment depression in short QT syndrome patients: a novel marker for diagnosing short QT syndrome?
Erol Tülümen, Carla Giustetto, Christian Wolpert, et al.
Circulation. Genomic and Precision Medicine
|
December 21, 2018
Reduced Na<sup>+</sup> Current in Native Cardiomyocytes of a Brugada Syndrome Patient Associated With β-2-Syntrophin Mutation
Constanze Schmidt, Felix Wiedmann, Ibrahim El-Battrawy, et al.
The American Journal of Cardiology
|
July 6, 2010
Usefulness of short-term variability of QT intervals as a predictor for electrical remodeling and proarrhythmia in patients with nonischemic heart failure
Martin Hinterseer, Britt-Maria Beckmann, Morten B Thomsen, et al.
Heart Rhythm
|
November 8, 2011
Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8
Hector Barajas-Martínez, Dan Hu, Tania Ferrer, et al.
Circulation
|
December 17, 2003
Sudden death associated with short-QT syndrome linked to mutations in HERG
Ramon Brugada, Kui Hong, Robert Dumaine, et al.
Heart Rhythm
|
December 14, 2011
A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents
Dan Hu, Hector Barajas-Martínez, Argelia Medeiros-Domingo, et al.
International Journal of Cardiology
|
January 21, 2014
ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene
Dan Hu, Hector Barajas-Martínez, Andre Terzic, et al.
Heart Rhythm
|
September 7, 2010
Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death
Elena 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 death
Charles Antzelevitch, Guido D Pollevick, Jonathan M Cordeiro, et al.
Journal of the American College of Cardiology
|
July 7, 2014
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
Dan Hu, Hector Barajas-Martínez, Ryan Pfeiffer, et al.
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Search research articles
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Showing results (81-90 of 91) with videos related to
Sort By:
Page
of 10
Heart Rhythm
|
April 29, 2014
Reply to the Editor--PQ-segment depression in short QT syndrome patients: a novel marker for diagnosing short QT syndrome?
Erol Tülümen, Carla Giustetto, Christian Wolpert, et al.
Circulation. Genomic and Precision Medicine
|
December 21, 2018
Reduced Na<sup>+</sup> Current in Native Cardiomyocytes of a Brugada Syndrome Patient Associated With β-2-Syntrophin Mutation
Constanze Schmidt, Felix Wiedmann, Ibrahim El-Battrawy, et al.
The American Journal of Cardiology
|
July 6, 2010
Usefulness of short-term variability of QT intervals as a predictor for electrical remodeling and proarrhythmia in patients with nonischemic heart failure
Martin Hinterseer, Britt-Maria Beckmann, Morten B Thomsen, et al.
Heart Rhythm
|
November 8, 2011
Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8
Hector Barajas-Martínez, Dan Hu, Tania Ferrer, et al.
Circulation
|
December 17, 2003
Sudden death associated with short-QT syndrome linked to mutations in HERG
Ramon Brugada, Kui Hong, Robert Dumaine, et al.
Heart Rhythm
|
December 14, 2011
A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents
Dan Hu, Hector Barajas-Martínez, Argelia Medeiros-Domingo, et al.
International Journal of Cardiology
|
January 21, 2014
ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene
Dan Hu, Hector Barajas-Martínez, Andre Terzic, et al.
Heart Rhythm
|
September 7, 2010
Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death
Elena 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 death
Charles Antzelevitch, Guido D Pollevick, Jonathan M Cordeiro, et al.
Journal of the American College of Cardiology
|
July 7, 2014
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome
Dan Hu, Hector Barajas-Martínez, Ryan Pfeiffer, et al.
Page
of 10