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Stephanie D Davis

Showing results (91-100 of 167) with videos related to

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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2022
Comparative analysis of respiratory symptom scores to detect acute respiratory events in children with cystic fibrosisLucy Perrem, Sanja Stanojevic, Michelle Shaw, et al.
The Laryngoscope|August 13, 2015
Volumetric nasal cavity analysis in children with unilateral and bilateral cleft lip and palateZainab Farzal, Jonathan Walsh, Gabriella Lopes de Rezende Barbosa, et al.
Annals of the American Thoracic Society|August 9, 2018
Tidal Breathing Measurements at Discharge and Clinical Outcomes in Extremely Low Gestational Age NeonatesClement L Ren, Rui Feng, Stephanie D Davis, et al.
The Lancet. Respiratory Medicine|January 28, 2014
Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D-CFTR mutation and preserved spirometry: a randomised controlled trialJane Davies, Helen Sheridan, Nicholas Bell, et al.
American Journal of Respiratory and Critical Care Medicine|December 16, 2024
Editorial Position of the American Thoracic Society Journal Family on the Evolving Role of Artificial Intelligence in Scientific Research and ReviewNitin Seam, Sanjay H Chotirmall, Fernando J Martinez, et al.
Plos One|May 16, 2017
Early childhood lung function is a stronger predictor of adolescent lung function in cystic fibrosis than early Pseudomonas aeruginosa infectionJessica E Pittman, Hannah Noah, Hollin E Calloway, et al.
Neurology|August 17, 2016
Sleep and pulmonary outcomes for clinical trials of airway plexiform neurofibromas in NF1Scott R Plotkin, Stephanie D Davis, Kent A Robertson, et al.
American Journal of Respiratory and Critical Care Medicine|February 17, 2007
Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosisStephanie D Davis, Lynn A Fordham, Alan S Brody, et al.
The Lancet. Respiratory Medicine|March 14, 2022
The effect of inhaled hypertonic saline on lung structure in children aged 3-6 years with cystic fibrosis (SHIP-CT): a multicentre, randomised, double-blind, controlled trialHarm A W M Tiddens, Yuxin Chen, Eleni-Rosalina Andrinopoulou, et al.
Pediatric Pulmonology|February 3, 2015
Novel outcome measures for clinical trials in cystic fibrosisHarm A W M Tiddens, Michael Puderbach, Jose G Venegas, et al.
Pageof 17

Showing results (91-100 of 167) with videos related to

Sort By:
Pageof 17
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2022
Comparative analysis of respiratory symptom scores to detect acute respiratory events in children with cystic fibrosisLucy Perrem, Sanja Stanojevic, Michelle Shaw, et al.
The Laryngoscope|August 13, 2015
Volumetric nasal cavity analysis in children with unilateral and bilateral cleft lip and palateZainab Farzal, Jonathan Walsh, Gabriella Lopes de Rezende Barbosa, et al.
Annals of the American Thoracic Society|August 9, 2018
Tidal Breathing Measurements at Discharge and Clinical Outcomes in Extremely Low Gestational Age NeonatesClement L Ren, Rui Feng, Stephanie D Davis, et al.
The Lancet. Respiratory Medicine|January 28, 2014
Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D-CFTR mutation and preserved spirometry: a randomised controlled trialJane Davies, Helen Sheridan, Nicholas Bell, et al.
American Journal of Respiratory and Critical Care Medicine|December 16, 2024
Editorial Position of the American Thoracic Society Journal Family on the Evolving Role of Artificial Intelligence in Scientific Research and ReviewNitin Seam, Sanjay H Chotirmall, Fernando J Martinez, et al.
Plos One|May 16, 2017
Early childhood lung function is a stronger predictor of adolescent lung function in cystic fibrosis than early Pseudomonas aeruginosa infectionJessica E Pittman, Hannah Noah, Hollin E Calloway, et al.
Neurology|August 17, 2016
Sleep and pulmonary outcomes for clinical trials of airway plexiform neurofibromas in NF1Scott R Plotkin, Stephanie D Davis, Kent A Robertson, et al.
American Journal of Respiratory and Critical Care Medicine|February 17, 2007
Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosisStephanie D Davis, Lynn A Fordham, Alan S Brody, et al.
The Lancet. Respiratory Medicine|March 14, 2022
The effect of inhaled hypertonic saline on lung structure in children aged 3-6 years with cystic fibrosis (SHIP-CT): a multicentre, randomised, double-blind, controlled trialHarm A W M Tiddens, Yuxin Chen, Eleni-Rosalina Andrinopoulou, et al.
Pediatric Pulmonology|February 3, 2015
Novel outcome measures for clinical trials in cystic fibrosisHarm A W M Tiddens, Michael Puderbach, Jose G Venegas, et al.
Pageof 17