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Circulation. Genomic and Precision Medicine|February 8, 2022
CELSR1 Risk Alleles in Familial Bicuspid Aortic Valve and Hypoplastic Left Heart SyndromeJeanne L Theis, Talha Niaz, Rhianna S Sundsbak, et al.Physiological Genomics|May 8, 2014
Transcriptional atlas of cardiogenesis maps congenital heart disease interactomeXing Li, Almudena Martinez-Fernandez, Katherine A Hartjes, et al.Heart (British Cardiac Society)|February 12, 2016
Spontaneous coronary artery dissection and its association with heritable connective tissue disordersStanislav Henkin, Sara M Negrotto, Marysia S Tweet, et al.Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|December 2, 2017
Characteristic Morphologies of the Bicuspid Aortic Valve in Patients with Genetic SyndromesTalha Niaz, Joseph T Poterucha, Timothy M Olson, et al.American Journal of Physiology. Heart and Circulatory Physiology|November 27, 2015
LRRC10 is required to maintain cardiac function in response to pressure overloadMatthew J Brody, Li Feng, Adrian C Grimes, et al.Plos One|January 28, 2014
A functional genetic variant (N521D) in natriuretic peptide receptor 3 is associated with diastolic dysfunction: the prevalence of asymptomatic ventricular dysfunction studyNaveen L Pereira, Margaret M Redfield, Christopher Scott, et al.JAMA Cardiology|May 7, 2020
Identification of Susceptibility Loci for Spontaneous Coronary Artery DissectionTamiel N Turley, Megan M O'Byrne, Matthew L Kosel, et al.Journal of Cardiovascular Development and Disease|September 27, 2023
Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological PathwaysTamiel N Turley, Jeanne L Theis, Jared M Evans, et al.The Annals of Thoracic Surgery|June 26, 2012
Late outcomes for surgical repair of supravalvar aortic stenosisSalil V Deo, Harold M Burkhart, Hartzell V Schaff, et al.Journal of the American College of Cardiology|August 29, 2009
Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathyKatharine M Brauch, Margaret L Karst, Kathleen J Herron, et al.Pageof 8