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UCSF School of Medicine | Department of Pediatrics UCSF Medical Center

Sociodemographic factors associated with tracheostomy and mortality in bronchopulmonary dysplasia.

  • Read more about 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.

  • Read more about 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.

  • Read more about 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.

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Respiratory medication use in extremely premature (<29 weeks) infants during initial NICU hospitalization: Results from the prematurity and respiratory outcomes program.

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Outcomes of pulmonary vascular disease in infants conceived with non-IVF fertility treatment and assisted reproductive technologies at 1 year of age.

  • Read more about 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.

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Mortality in infants with bronchopulmonary dysplasia: Data from cardiac catheterization.

  • Read more about 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.

  • Read more about A novel, noninvasive assay shows that distal airway oxygen tension is low in cystic fibrosis, but not in primary ciliary dyskinesia.

Case report: Giant cystic lesions with a rare pulmonary diagnosis.

  • Read more about Case report: Giant cystic lesions with a rare pulmonary diagnosis.

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