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Circulation. Arrhythmia and Electrophysiology
|
April 14, 2017
Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test Referrals
Andrew P Landstrom, Andrew L Dailey-Schwartz, Jill A Rosenfeld, et al.
Journal of the American College of Cardiology
|
August 27, 2013
Mutation E169K in junctophilin-2 causes atrial fibrillation due to impaired RyR2 stabilization
David L Beavers, Wei Wang, Sameer Ather, et al.
Pediatric Cardiology
|
March 8, 2024
Obesity Predisposes Anthracycline-Treated Survivors of Childhood and Adolescent Cancers to Subclinical Cardiac Dysfunction
Ian A George, BriAnna Souder, Amy Berkman, et al.
American Journal of Medical Genetics. Part A
|
December 28, 2020
TBX5-encoded T-box transcription factor 5 variant T223M is associated with long QT syndrome and pediatric sudden cardiac death
Alexandra M Markunas, Perathu K R Manivannan, Jordan E Ezekian, et al.
Journal of Cardiac Failure
|
October 19, 2019
Association of Wolff-Parkinson-White With Left Ventricular Noncompaction Cardiomyopathy in Children
Taylor S Howard, Santiago O Valdes, Kyle D Hope, et al.
Pediatric Research
|
July 5, 2024
Cardiovascular disease risk factors in congenital heart disease survivors are associated with heart failure
Andrew P Landstrom, Tracy Spears, Alfred D'Ottavio, et al.
Circulation
|
November 15, 2021
Inflammation and Immune Response in Arrhythmogenic Cardiomyopathy: State-of-the-Art Review
Babken Asatryan, Angeliki Asimaki, Andrew P Landstrom, et al.
Journal of Cellular and Molecular Medicine
|
June 10, 2021
Efficacy of RyR2 inhibitor EL20 in induced pluripotent stem cell-derived cardiomyocytes from a patient with catecholaminergic polymorphic ventricular tachycardia
Tarah A Word, Ann P Quick, Christina Y Miyake, et al.
Journal of Molecular and Cellular Cardiology
|
April 13, 2020
Meta-analysis of cardiomyopathy-associated variants in troponin genes identifies loci and intragenic hot spots that are associated with worse clinical outcomes
Hanna J Tadros, Chelsea S Life, Gustavo Garcia, et al.
Journal of the American Heart Association
|
February 27, 2020
Variant R94C in <i>TNNT2</i>-Encoded Troponin T Predisposes to Pediatric Restrictive Cardiomyopathy and Sudden Death Through Impaired Thin Filament Relaxation Resulting in Myocardial Diastolic Dysfunction
Jordan E Ezekian, Sarah R Clippinger, Jaquelin M Garcia, et al.
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Search research articles
Search
Showing results (61-70 of 113) with videos related to
Sort By:
Page
of 12
Circulation. Arrhythmia and Electrophysiology
|
April 14, 2017
Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test Referrals
Andrew P Landstrom, Andrew L Dailey-Schwartz, Jill A Rosenfeld, et al.
Journal of the American College of Cardiology
|
August 27, 2013
Mutation E169K in junctophilin-2 causes atrial fibrillation due to impaired RyR2 stabilization
David L Beavers, Wei Wang, Sameer Ather, et al.
Pediatric Cardiology
|
March 8, 2024
Obesity Predisposes Anthracycline-Treated Survivors of Childhood and Adolescent Cancers to Subclinical Cardiac Dysfunction
Ian A George, BriAnna Souder, Amy Berkman, et al.
American Journal of Medical Genetics. Part A
|
December 28, 2020
TBX5-encoded T-box transcription factor 5 variant T223M is associated with long QT syndrome and pediatric sudden cardiac death
Alexandra M Markunas, Perathu K R Manivannan, Jordan E Ezekian, et al.
Journal of Cardiac Failure
|
October 19, 2019
Association of Wolff-Parkinson-White With Left Ventricular Noncompaction Cardiomyopathy in Children
Taylor S Howard, Santiago O Valdes, Kyle D Hope, et al.
Pediatric Research
|
July 5, 2024
Cardiovascular disease risk factors in congenital heart disease survivors are associated with heart failure
Andrew P Landstrom, Tracy Spears, Alfred D'Ottavio, et al.
Circulation
|
November 15, 2021
Inflammation and Immune Response in Arrhythmogenic Cardiomyopathy: State-of-the-Art Review
Babken Asatryan, Angeliki Asimaki, Andrew P Landstrom, et al.
Journal of Cellular and Molecular Medicine
|
June 10, 2021
Efficacy of RyR2 inhibitor EL20 in induced pluripotent stem cell-derived cardiomyocytes from a patient with catecholaminergic polymorphic ventricular tachycardia
Tarah A Word, Ann P Quick, Christina Y Miyake, et al.
Journal of Molecular and Cellular Cardiology
|
April 13, 2020
Meta-analysis of cardiomyopathy-associated variants in troponin genes identifies loci and intragenic hot spots that are associated with worse clinical outcomes
Hanna J Tadros, Chelsea S Life, Gustavo Garcia, et al.
Journal of the American Heart Association
|
February 27, 2020
Variant R94C in <i>TNNT2</i>-Encoded Troponin T Predisposes to Pediatric Restrictive Cardiomyopathy and Sudden Death Through Impaired Thin Filament Relaxation Resulting in Myocardial Diastolic Dysfunction
Jordan E Ezekian, Sarah R Clippinger, Jaquelin M Garcia, et al.
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of 12