Showing results (51-60 of 180) with videos related to
Sort By:
Pageof 18
Plos One|July 18, 2019
Gene-based genome-wide association studies and meta-analyses of conotruncal heart defectsAnshuman Sewda, A J Agopian, Elizabeth Goldmuntz, et al.Pediatric Cardiology|December 19, 2014
The impact of pulmonary insufficiency on the right ventricle: a comparison of isolated valvar pulmonary stenosis and tetralogy of fallotLaura Mercer-Rosa, Eitan Ingall, Xuemei Zhang, et al.Journal of Cardiovascular Imaging|January 27, 2022
Right Ventricular Strain Is Associated With Increased Length of Stay After Tetralogy of Fallot RepairRanjini Srinivasan, Jennifer A Faerber, Grace DeCost, et al.Pediatric Cardiology|June 8, 2018
Perioperative Factors Influence the Long-Term Outcomes of Children and Adolescents with Repaired Tetralogy of FallotLaura Mercer-Rosa, Xuemei Zhang, Ronn E Tanel, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|September 5, 2008
Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndromeElizabeth Goldmuntz, Deborah A Driscoll, Beverly S Emanuel, et al.Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|April 9, 2018
Longitudinal Changes in Right Ventricular Function in Tetralogy of Fallot in the Initial Years after Surgical RepairMichael P DiLorenzo, Okan U Elci, Yan Wang, et al.Circulation|November 13, 2002
Analysis of cardiovascular phenotype and genotype-phenotype correlation in individuals with a JAG1 mutation and/or Alagille syndromeDoff B McElhinney, Ian D Krantz, Lynn Bason, et al.Plos One|June 10, 2020
Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defectsAnshuman Sewda, A J Agopian, Elizabeth Goldmuntz, et al.Pediatric Cardiology|April 23, 2013
22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive casesShabnam Peyvandi, Philip J Lupo, Jennifer Garbarini, et al.Congenital Heart Disease|October 21, 2011
Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomaliesElizabeth Goldmuntz, Prasuna Paluru, Joseph Glessner, et al.Pageof 18