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The American Journal of Cardiology|December 12, 2022
Cardiopulmonary Exercise Testing in Athletes With Hypertrophic CardiomyopathyDarrell B Newman, Ramin Garmany, Alejandra Meza Contreras, et al.
Journal of Medical Genetics|March 8, 2017
KCNQ1 p.L353L affects splicing and modifies the phenotype in a founder population with long QT syndrome type 1Jamie D Kapplinger, Anders Erickson, Sirisha Asuri, et al.
Cardiovascular Research|September 28, 2007
A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardiaBi-Hua Tan, Pedro Iturralde-Torres, Argelia Medeiros-Domingo, et al.
Acta Cardiologica|March 8, 2018
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathySalma I Patel, Michael J Ackerman, Fadi E Shamoun, et al.
Journal of Molecular and Cellular Cardiology|June 24, 2008
Molecular and functional characterization of novel hypertrophic cardiomyopathy susceptibility mutations in TNNC1-encoded troponin CAndrew P Landstrom, Michelle S Parvatiyar, Jose R Pinto, et al.
Cardiovascular Digital Health Journal|January 2, 2023
Tandem deep learning and logistic regression models to optimize hypertrophic cardiomyopathy detection in routine clinical practiceMaren Maanja, Peter A Noseworthy, Jeffrey B Geske, et al.
Circulation|January 28, 2021
Suppression-Replacement KCNQ1 Gene Therapy for Type 1 Long QT SyndromeSteven M Dotzler, C S John Kim, William A C Gendron, et al.
The Journal of Pediatrics|August 10, 2016
Clinical Presentation of Pediatric Patients at Risk for Sudden Cardiac ArrestAarti Dalal, Richard J Czosek, Joshua Kovach, et al.
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