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Pacing and Clinical Electrophysiology : PACE
|
February 20, 2024
Ion channel dysfunction and fibrosis in atrial fibrillation: Two sides of the same coin
Gianmarco Arabia, Maria Giulia Bellicini, Angelica Cersosimo, et al.
Nature Reviews. Genetics
|
October 7, 2024
Genome-wide association testing beyond SNPs
Laura Harris, Ellen M McDonagh, Xiaolei Zhang, et al.
European Journal of Preventive Cardiology
|
November 9, 2019
Sex-related differences in exercise performance and outcome of patients with hypertrophic cardiomyopathy
Luca Ghiselli, Alberto Marchi, Carlo Fumagalli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 8, 2018
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center
Francesco Mazzarotto, Francesca Girolami, Beatrice Boschi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 18, 2016
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
Roddy Walsh, Kate L Thomson, James S Ware, et al.
JMIR Medical Informatics
|
February 2, 2022
Disease Progression of Hypertrophic Cardiomyopathy: Modeling Using Machine Learning
Matej Pičulin, Tim Smole, Bojan Žunkovič, et al.
Computers in Biology and Medicine
|
July 19, 2021
A machine learning-based risk stratification model for ventricular tachycardia and heart failure in hypertrophic cardiomyopathy
Tim Smole, Bojan Žunkovič, Matej Pičulin, et al.
European Heart Journal
|
September 24, 2021
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death
Roddy Walsh, Arnon Adler, Ahmad S Amin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 30, 2021
Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation
Andrea D Thompson, Adam S Helms, Anamika Kannan, et al.
Frontiers in Physiology
|
November 24, 2022
Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: The impact of full-length dystrophin deficiency
Josè Manuel Pioner, Lorenzo Santini, Chiara Palandri, et al.
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Search research articles
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Showing results (11-20 of 41) with videos related to
Sort By:
Page
of 5
Pacing and Clinical Electrophysiology : PACE
|
February 20, 2024
Ion channel dysfunction and fibrosis in atrial fibrillation: Two sides of the same coin
Gianmarco Arabia, Maria Giulia Bellicini, Angelica Cersosimo, et al.
Nature Reviews. Genetics
|
October 7, 2024
Genome-wide association testing beyond SNPs
Laura Harris, Ellen M McDonagh, Xiaolei Zhang, et al.
European Journal of Preventive Cardiology
|
November 9, 2019
Sex-related differences in exercise performance and outcome of patients with hypertrophic cardiomyopathy
Luca Ghiselli, Alberto Marchi, Carlo Fumagalli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 8, 2018
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center
Francesco Mazzarotto, Francesca Girolami, Beatrice Boschi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 18, 2016
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
Roddy Walsh, Kate L Thomson, James S Ware, et al.
JMIR Medical Informatics
|
February 2, 2022
Disease Progression of Hypertrophic Cardiomyopathy: Modeling Using Machine Learning
Matej Pičulin, Tim Smole, Bojan Žunkovič, et al.
Computers in Biology and Medicine
|
July 19, 2021
A machine learning-based risk stratification model for ventricular tachycardia and heart failure in hypertrophic cardiomyopathy
Tim Smole, Bojan Žunkovič, Matej Pičulin, et al.
European Heart Journal
|
September 24, 2021
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death
Roddy Walsh, Arnon Adler, Ahmad S Amin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 30, 2021
Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation
Andrea D Thompson, Adam S Helms, Anamika Kannan, et al.
Frontiers in Physiology
|
November 24, 2022
Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: The impact of full-length dystrophin deficiency
Josè Manuel Pioner, Lorenzo Santini, Chiara Palandri, et al.
Page
of 5