Dr. Jennifer L Taylor-cousar M.D.
Pulmonologist (Pediatric) | Pediatric Pulmonology
1400 Jackson St National Jewish Heal Denver CO, 80206About
Dr. Jennifer Taylor-cousar practices Pediatric Pulmonology in Denver, CO. Dr. Taylor-cousar treats children who have breathing problems, or a problem with his or her lungs. Pediatric pulmonologists often treat children with chronic cough, difficulty breathing, recurring pneumonia, asthma, cystic fibrosis, apnea, chronic lung disease in premature infants, noisy breathing, and conditions that require special equipment to monitor and/or help with breathing at home.
Board Certification
Internal MedicineAmerican Board of Internal MedicineABIM- Pulmonary Disease
PediatricsAmerican Board of PediatricsABP- Pediatric Pulmonology
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Pharmacological modulation of cGMP levels by phosphodiesterase 5 inhibitors as a therapeutic strategy for treatment of respiratory pathology in cystic fibrosis.
- Elevated furin levels in human cystic fibrosis cells result in hypersusceptibility to exotoxin A-induced cytotoxicity.
- Hypoventilation in cystic fibrosis.
- Effects of gender and age at diagnosis on disease progression in long-term survivors of cystic fibrosis.
- Potential of anti-inflammatory treatment for cystic fibrosis lung disease.
- Blood mRNA biomarkers for detection of treatment response in acute pulmonary exacerbations of cystic fibrosis.
- Azithromycin may antagonize inhaled tobramycin when targeting Pseudomonas aeruginosa in cystic fibrosis.
- Comparison of radiographic and clinical characteristics of low-risk and high-risk cystic fibrosis genotypes.
- Lumacaftor and ivacaftor in the management of patients with cystic fibrosis: current evidence and future prospects.
- SINUSITIS, BRONCHIECTASIS, AND FLATUS IN A SUMATRAN ORANGUTAN (PONGO ABELII): COULD THIS BE CYSTIC FIBROSIS?
- Pregnancy among cystic fibrosis women in the era of CFTR modulators.
- Pharmacokinetics and safety of cavosonstat (N91115) in healthy and cystic fibrosis adults homozygous for F508DEL-CFTR.
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