Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Stephanie D Davis

Showing results (101-110 of 167) with videos related to

Pageof 17
Sort By:
Pediatric Pulmonology|November 15, 2011
Lung function distinguishes preschool children with CF from healthy controls in a multi-center settingGwendolyn S Kerby, Margaret Rosenfeld, Clement L Ren, et al.
ERJ Open Research|May 1, 2018
The clinical utility of lung clearance index in early cystic fibrosis lung disease is not impacted by the number of multiple-breath washout trialsRachel E Foong, Alana J Harper, Billy Skoric, et al.
Pediatric Pulmonology|January 4, 2011
Age of Pseudomonas aeruginosa acquisition and subsequent severity of cystic fibrosis lung diseaseJessica E Pittman, Elizabeth H Calloway, Michelle Kiser, et al.
Annals of the American Thoracic Society|May 9, 2017
Multiple-Breath Washout Outcomes Are Sensitive to Inflammation and Infection in Children with Cystic FibrosisKathryn A Ramsey, Rachel E Foong, Jasmine Grdosic, et al.
Pediatric Pulmonology|November 15, 2011
Analysis of the associations between lung function and clinical features in preschool children with cystic fibrosisClement L Ren, Margaret Rosenfeld, Oscar H Mayer, et al.
Pediatric Pulmonology|November 15, 2021
Pulmonary function tests in extremely low gestational age infants at one year of ageJudith A Voynow, Rui Feng, Clement L Ren, et al.
Human Mutation|June 26, 2013
Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesiaM Leigh Anne Daniels, Margaret W Leigh, Stephanie D Davis, et al.
American Journal of Respiratory and Critical Care Medicine|December 13, 2016
Progression of Lung Disease in Preschool Patients with Cystic FibrosisSanja Stanojevic, Stephanie D Davis, George Retsch-Bogart, et al.
Chest|June 5, 2026
Accuracy of clinical phenotype for diagnosing adults with primary ciliary dyskinesiaAmanda Marino, Zofia N Zysman-Colman, Joy Agbonze, et al.
The Journal of Pediatrics|November 17, 2009
Cystic Fibrosis Foundation practice guidelines for the management of infants with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome during the first two years of life and beyond, Drucy Borowitz, Richard B Parad, et al.
Pageof 17

Showing results (101-110 of 167) with videos related to

Sort By:
Pageof 17
Pediatric Pulmonology|November 15, 2011
Lung function distinguishes preschool children with CF from healthy controls in a multi-center settingGwendolyn S Kerby, Margaret Rosenfeld, Clement L Ren, et al.
ERJ Open Research|May 1, 2018
The clinical utility of lung clearance index in early cystic fibrosis lung disease is not impacted by the number of multiple-breath washout trialsRachel E Foong, Alana J Harper, Billy Skoric, et al.
Pediatric Pulmonology|January 4, 2011
Age of Pseudomonas aeruginosa acquisition and subsequent severity of cystic fibrosis lung diseaseJessica E Pittman, Elizabeth H Calloway, Michelle Kiser, et al.
Annals of the American Thoracic Society|May 9, 2017
Multiple-Breath Washout Outcomes Are Sensitive to Inflammation and Infection in Children with Cystic FibrosisKathryn A Ramsey, Rachel E Foong, Jasmine Grdosic, et al.
Pediatric Pulmonology|November 15, 2011
Analysis of the associations between lung function and clinical features in preschool children with cystic fibrosisClement L Ren, Margaret Rosenfeld, Oscar H Mayer, et al.
Pediatric Pulmonology|November 15, 2021
Pulmonary function tests in extremely low gestational age infants at one year of ageJudith A Voynow, Rui Feng, Clement L Ren, et al.
Human Mutation|June 26, 2013
Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesiaM Leigh Anne Daniels, Margaret W Leigh, Stephanie D Davis, et al.
American Journal of Respiratory and Critical Care Medicine|December 13, 2016
Progression of Lung Disease in Preschool Patients with Cystic FibrosisSanja Stanojevic, Stephanie D Davis, George Retsch-Bogart, et al.
Chest|June 5, 2026
Accuracy of clinical phenotype for diagnosing adults with primary ciliary dyskinesiaAmanda Marino, Zofia N Zysman-Colman, Joy Agbonze, et al.
The Journal of Pediatrics|November 17, 2009
Cystic Fibrosis Foundation practice guidelines for the management of infants with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome during the first two years of life and beyond, Drucy Borowitz, Richard B Parad, et al.
Pageof 17