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Pediatric Pulmonology|September 17, 2020
Drug development for cystic fibrosisDon B Sanders, James F ChmielAnnals of the American Thoracic Society|January 21, 2021
Early-Life Height Attainment in Cystic Fibrosis Is Associated with Pulmonary Function at Age 6 YearsDon B Sanders, James E Slaven, Karen Maguiness, et al.BMJ Open Respiratory Research|March 27, 2026
Registry-based study of gastrostomy tube placement and nutritional recovery in children with cystic fibrosisBrittany Wall, James E Slaven, Molly A Bozic, et al.International Journal of Neonatal Screening|March 28, 2023
Immunoreactive Trypsinogen in Infants Born to Women with Cystic Fibrosis Taking Elexacaftor-Tezacaftor-IvacaftorPayal Patel, Jana Yeley, Cynthia Brown, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 17, 2023
Nasal airway inflammatory responses and pathogen detection in infants with cystic fibrosisBenjamin T Kopp, Sydney E Ross, Dinesh Bojja, et al.Pediatric Clinics of North America|July 30, 2016
Background and EpidemiologyDon B Sanders, Aliza K FinkRespiratory Research|September 27, 2003
State of the art: why do the lungs of patients with cystic fibrosis become infected and why can't they clear the infection?James F Chmiel, Pamela B DavisClinics in Chest Medicine|May 1, 2007
Inflammation and anti-inflammatory therapies for cystic fibrosisJames F Chmiel, Michael W KonstanTreatments in Respiratory Medicine|August 10, 2005
Anti-inflammatory medications for cystic fibrosis lung disease: selecting the most appropriate agentJames F Chmiel, Michael W KonstanPediatric Pulmonology|September 4, 2015
Inflammation and its genesis in cystic fibrosisDavid P Nichols, James F ChmielPageof 12