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Journal of Cardiovascular Electrophysiology
|
February 6, 2010
Comparative expression of proteins in left and right atrial appendages from patients with mitral valve disease at sinus rhythm and atrial fibrillation
Javier Modrego, Luis Maroto, Juan Tamargo, et al.
Biochemical Pharmacology
|
May 8, 2013
Propafenone blocks human cardiac Kir2.x channels by decreasing the negative electrostatic charge in the cytoplasmic pore
Irene Amorós, Pablo Dolz-Gaitón, Ricardo Gómez, et al.
Circulation. Arrhythmia and Electrophysiology
|
January 6, 2009
Functional effects of KCNE3 mutation and its role in the development of Brugada syndrome
Eva Delpón, Jonathan M Cordeiro, Lucía Núñez, et al.
Proteomics. Clinical Applications
|
December 8, 2010
Modifications by Olmesartan medoxomil treatment of the platelet protein profile of moderate hypertensive patients
Daniel Sacristán, María Marques, José J Zamorano-León, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 30, 2023
A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish family
Anabel Cámara-Checa, Francesca Perin, Marcos Rubio-Alarcón, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 18, 2010
Flecainide increases Kir2.1 currents by interacting with cysteine 311, decreasing the polyamine-induced rectification
Ricardo Caballero, Pablo Dolz-Gaitón, Ricardo Gómez, et al.
Heart Rhythm
|
November 27, 2010
Functional effects of a missense mutation in HERG associated with type 2 long QT syndrome
Irene Amorós, Juan Jiménez-Jáimez, Luis Tercedor, et al.
Journal of the American College of Cardiology
|
May 22, 2010
In humans, chronic atrial fibrillation decreases the transient outward current and ultrarapid component of the delayed rectifier current differentially on each atria and increases the slow component of the delayed rectifier current in both
Ricardo Caballero, Marta González de la Fuente, Ricardo Gómez, et al.
Revista Espanola De Cardiologia (English Ed.)
|
April 26, 2018
Digenic Heterozigosity in SCN5A and CACNA1C Explains the Variable Expressivity of the Long QT Phenotype in a Spanish Family
Paloma Nieto-Marín, Juan Jiménez-Jáimez, David Tinaquero, et al.
Plos One
|
December 24, 2013
Functional characterization of a novel frameshift mutation in the C-terminus of the Nav1.5 channel underlying a Brugada syndrome with variable expression in a Spanish family
Pablo Dolz-Gaitón, Mercedes Núñez, Lucía Núñez, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 81) with videos related to
Sort By:
Page
of 9
Journal of Cardiovascular Electrophysiology
|
February 6, 2010
Comparative expression of proteins in left and right atrial appendages from patients with mitral valve disease at sinus rhythm and atrial fibrillation
Javier Modrego, Luis Maroto, Juan Tamargo, et al.
Biochemical Pharmacology
|
May 8, 2013
Propafenone blocks human cardiac Kir2.x channels by decreasing the negative electrostatic charge in the cytoplasmic pore
Irene Amorós, Pablo Dolz-Gaitón, Ricardo Gómez, et al.
Circulation. Arrhythmia and Electrophysiology
|
January 6, 2009
Functional effects of KCNE3 mutation and its role in the development of Brugada syndrome
Eva Delpón, Jonathan M Cordeiro, Lucía Núñez, et al.
Proteomics. Clinical Applications
|
December 8, 2010
Modifications by Olmesartan medoxomil treatment of the platelet protein profile of moderate hypertensive patients
Daniel Sacristán, María Marques, José J Zamorano-León, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 30, 2023
A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish family
Anabel Cámara-Checa, Francesca Perin, Marcos Rubio-Alarcón, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 18, 2010
Flecainide increases Kir2.1 currents by interacting with cysteine 311, decreasing the polyamine-induced rectification
Ricardo Caballero, Pablo Dolz-Gaitón, Ricardo Gómez, et al.
Heart Rhythm
|
November 27, 2010
Functional effects of a missense mutation in HERG associated with type 2 long QT syndrome
Irene Amorós, Juan Jiménez-Jáimez, Luis Tercedor, et al.
Journal of the American College of Cardiology
|
May 22, 2010
In humans, chronic atrial fibrillation decreases the transient outward current and ultrarapid component of the delayed rectifier current differentially on each atria and increases the slow component of the delayed rectifier current in both
Ricardo Caballero, Marta González de la Fuente, Ricardo Gómez, et al.
Revista Espanola De Cardiologia (English Ed.)
|
April 26, 2018
Digenic Heterozigosity in SCN5A and CACNA1C Explains the Variable Expressivity of the Long QT Phenotype in a Spanish Family
Paloma Nieto-Marín, Juan Jiménez-Jáimez, David Tinaquero, et al.
Plos One
|
December 24, 2013
Functional characterization of a novel frameshift mutation in the C-terminus of the Nav1.5 channel underlying a Brugada syndrome with variable expression in a Spanish family
Pablo Dolz-Gaitón, Mercedes Núñez, Lucía Núñez, et al.
Page
of 9