Dr. John P Clancy M.D.
Pulmonologist (Pediatric) | Pediatric Pulmonology
3333 Burnet Ave. , Ml 2021 Cincinnati Children' Cincinnati OH, 45229About
Dr. John Clancy practices Pediatric Pulmonology in Cincinnati, OH. Dr. Clancy 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.
Education and Training
Baylor College of Medicine, Houston, Texas 1990
Provider Details
Expert Publications
Data provided by the National Library of Medicine- A macromolecular complex of beta 2 adrenergic receptor, CFTR, and ezrin/radixin/moesin-binding phosphoprotein 50 is regulated by PKA.
- Adenosine receptors and phosphodiesterase inhibitors stimulate Cl- secretion in Calu-3 cells.
- The Caregiver Quality of Life Cystic Fibrosis (CQOLCF) scale: modification and validation of an instrument to measure quality of life in cystic fibrosis family caregivers.
- Mutations in the amino terminus of the cystic fibrosis transmembrane conductance regulator enhance endocytosis.
- Advances in cystic fibrosis therapies.
- Restoration of W1282X CFTR activity by enhanced expression.
- Detection of cystic fibrosis transmembrane conductance regulator activity in early-phase clinical trials.
- Pharmaceuticals targeting nonsense mutations in genetic diseases: progress in development.
- Extracorporeal membrane oxygenation causes loss of intestinal epithelial barrier in the newborn piglet.
- Personalized medicine in cystic fibrosis: dawning of a new era.
- Optimizing nasal potential difference analysis for CFTR modulator development: assessment of ivacaftor in CF subjects with the G551D-CFTR mutation.
- Ivacaftor treatment of cystic fibrosis patients with the G551D mutation: a review of the evidence.
- A semiparametric approach to estimate rapid lung function decline in cystic fibrosis.
- Pulmonary matrix metalloproteinase-9 activity in mechanically ventilated children with respiratory syncytial virus.
- Nebulized liposomal amikacin for the treatment of Pseudomonas aeruginosa infection in cystic fibrosis patients.
Clinical Trials
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