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The Pediatric Infectious Disease Journal|April 16, 2014
Acute myopericarditis associated with cat scratch disease in an adolescentWilliam J Barson, J Robert Honegger, Karen Texter
The Pediatric Infectious Disease Journal|April 14, 2017
Multiorgan Involvement Confounding the Diagnosis of Bartonella henselae Infective Endocarditis in Children With Congenital Heart DiseaseChristopher P Ouellette, Sarita Joshi, Karen Texter, et al.
The Journal of Pediatrics|March 16, 2015
Diagnosis of systemic-onset juvenile idiopathic arthritis after treatment for presumed Kawasaki diseaseSiwen Dong, Sharon Bout-Tabaku, Karen Texter, et al.
International Journal of Cardiology|December 2, 2019
Serial fetal echocardiograms in hypoplastic left heart syndrome fetuses: Does it affect immediate post-natal care?Bernadette Richards, Lesley Freel, Corey Stiver, et al.
Birth Defects Research|February 24, 2022
Probing single ventricle heart defects with patient-derived induced pluripotent stem cells and emerging technologiesBailey Hall, Matthew Alonzo, Karen Texter, et al.
Pediatric Cardiology|November 3, 2019
Early Integration of Palliative Care in Families of Children with Single Ventricle Congenital Heart Defects: A Quality Improvement Project to Enhance Family SupportJo Ann M Davis, Alice Bass, Lisa Humphrey, et al.
Annals of Thoracic Surgery Short Reports|January 10, 2025
Efficiency at Heart: Navigating the Hybrid Single-Ventricle PathwayDariya Hardisky, Divyaam Satija, Karen Texter, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|July 17, 2007
Persistence of bilateral arterial ducts in pulmonary atresia despite confluent branch pulmonary arteries: opportunity for two percutaneous therapeutic alternativesKaren Texter, Anjan Shah, Karina Carlson, et al.
Stem Cell Research|July 2, 2023
Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defectsMatthew Alonzo, Shiqiao Ye, Brian Beckman, et al.
Stem Cell Research|January 4, 2023
Establishment of NCHi009-A, an iPSC line from a patient with hypoplastic left heart syndrome (HLHS) carrying a heterozygous NOTCH1 mutationSubhodip Adhicary, Shiqiao Ye, Hui Lin, et al.
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