Fellowship · Salt Lake City, UT
Sponsored by University of Utah Health
The global prevalence and ethnic heterogeneity of primary ciliary dyskinesia gene variants: a genetic database analysis.
The Lancet. Respiratory medicine · 2022 · 183 citations · Kristen Ameel
Inhaled mRNA therapy for treatment of cystic fibrosis: Interim results of a randomized, double-blind, placebo-controlled phase 1/2 clinical study.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2023 · 116 citations · Theodore Liou
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features.
The Journal of clinical investigation · 2024 · 43 citations · Khanh Lai
Respiratory Outcomes for Ventilator-Dependent Children With Bronchopulmonary Dysplasia.
Pediatrics · 2023 · 31 citations · Khanh Lai
Outcomes of infants and children with bronchopulmonary dysplasia-associated pulmonary hypertension who required home ventilation.
Pediatric research · 2025 · 11 citations · Khanh Lai
Impact of CFTR Modulators on Longitudinal Cystic Fibrosis Survival and Mortality: Review and Secondary Analysis.
Pulmonary therapy · 2025 · 12 citations · Theodore Liou
Approaches to Interdisciplinary Care for Infants with Severe Bronchopulmonary Dysplasia: A Survey of the Bronchopulmonary Dysplasia Collaborative.
American journal of perinatology · 2024 · 11 citations · Khanh Lai
A Phase 3, Open-Label Study of Lumacaftor/Ivacaftor in Children 1 to Less Than 2 Years of Age with Cystic Fibrosis Homozygous for F508del-CFTR.
American journal of respiratory and critical care medicine · 2022 · 34 citations · Fadi Asfour