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PAMELA ZEITLIN, M.D.
M.D.
Pediatric Pulmonology Physician
NPI: 1346278801Individual
Specialties, Licenses & Credentials
Pediatric Pulmonology PhysicianPrimary
Pediatrics — Pediatric Pulmonology
Code: 2080P0214X
D33202(MD)0057811(CO)
Research & Publications (20)
Pseudomonas aeruginosa: can studies in engineered cells tell us why is it such a problem in people with cystic fibrosis? Focus on "Cystic fibrosis transmembrane conductance regulator and caveolin-1 regulate epithelial cell internalization of Pseudomonas aeruginosa".
PMID 19553563·Am J Physiol Cell Physiol·2009
8-other
The penetration of fresh undiluted sputum expectorated by cystic fibrosis patients by non-adhesive polymer nanoparticles.
PMID 19176245·Biomaterials·2009
8-other
Proteome of synaptosome-associated proteins in spinal cord dorsal horn after peripheral nerve injury.
PMID 19206110·Proteomics·2009
7-preclinical
Spiperone, identified through compound screening, activates calcium-dependent chloride secretion in the airway.
PMID 18987251·Am J Physiol Cell Physiol·2009
7-preclinical
CFTR is a negative regulator of NFkappaB mediated innate immune response.
PMID 19247502·PLoS One·2009
7-preclinical
Lubiprostone activates non-CFTR-dependent respiratory epithelial chloride secretion in cystic fibrosis mice.
PMID 18805957·Am J Physiol Lung Cell Mol Physiol·2008
7-preclinical
Chemical rescue of deltaF508-CFTR mimics genetic repair in cystic fibrosis bronchial epithelial cells.
PMID 18285607·Mol Cell Proteomics·2008
8-other
Dietary supplement use in pediatric patients with cystic fibrosis.
PMID 18319503·Am J Health Syst Pharm·2008
8-other
Atypical cystic fibrosis and CFTR-related diseases.
PMID 18493878·Clin Rev Allergy Immunol·2008
6-review
Cystic fibrosis presenting as recurrent pancreatitis in a young child with a normal sweat test and pancreas divisum: a case report.
PMID 18501000·J Med Case Rep·2008
8-other
Pulmonary function in adolescents with ataxia telangiectasia.
PMID 18041755·Pediatr Pulmonol·2008
8-other
Current treatment recommendations for correcting vitamin D deficiency in pediatric patients with cystic fibrosis are inadequate.
PMID 18589445·J Pediatr·2008
8-other
CHOP transcription factor mediates IL-8 signaling in cystic fibrosis bronchial epithelial cells.
PMID 17709599·Am J Respir Cell Mol Biol·2008
8-other
No detectable improvements in cystic fibrosis transmembrane conductance regulator by nasal aminoglycosides in patients with cystic fibrosis with stop mutations.
PMID 17347447·Am J Respir Cell Mol Biol·2007
4-observational
Duration of treatment effect after tobramycin solution for inhalation in young children with cystic fibrosis.
PMID 17534969·Pediatr Pulmonol·2007
8-other
Patients with mutations in Gsalpha have reduced activation of a downstream target in epithelial tissues due to haploinsufficiency.
PMID 17652219·J Clin Endocrinol Metab·2007
8-other
Repeated aerosolized AAV-CFTR for treatment of cystic fibrosis: a randomized placebo-controlled phase 2B trial.
PMID 17685853·Hum Gene Ther·2007
3-trial
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1400 JACKSON ST
DENVER, CO 80206 - Phone
- (303) 388-4461
Quick Facts
- NPI
- 1346278801
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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