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How Many Billions Is Enough? Prioritizing Profits Over Patients With Cystic Fibrosis.
Sociodemographic factors associated with tracheostomy and mortality in bronchopulmonary dysplasia.
Pulmonary hypertension is an important co-morbidity in developmental lung diseases of infancy: Bronchopulmonary dysplasia and congenital diaphragmatic hernia.
Association of patient weight status with plasma surfactant protein D, a biomarker of alveolar epithelial injury, in children with acute respiratory failure.
The many faces and outcomes of pulmonary vein stenosis in early childhood.
Respiratory medication use in extremely premature (<29 weeks) infants during initial NICU hospitalization: Results from the prematurity and respiratory outcomes program.
Outcomes of pulmonary vascular disease in infants conceived with non-IVF fertility treatment and assisted reproductive technologies at 1 year of age.
Regional variations in longitudinal pulmonary function: A comparison of Hispanic and non-Hispanic subjects with cystic fibrosis in the United States.
Mortality in infants with bronchopulmonary dysplasia: Data from cardiac catheterization.
A novel, noninvasive assay shows that distal airway oxygen tension is low in cystic fibrosis, but not in primary ciliary dyskinesia.