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Pediatric Research
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October 13, 2010
Skeletal muscle metabolism in cystic fibrosis and primary ciliary dyskinesia
Greg D Wells, Donna L Wilkes, Jane E Schneiderman, et al.
Annals of the American Thoracic Society
|
July 10, 2020
Clinical Effectiveness of Lumacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for F508del-CFTR. A Clinical Trial
Scott D Sagel, Umer Khan, Sonya L Heltshe, 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 trial
Harm A W M Tiddens, Yuxin Chen, Eleni-Rosalina Andrinopoulou, et al.
Plos One
|
June 16, 2016
A Systematic Approach to Multiple Breath Nitrogen Washout Test Quality
Renee Jensen, Sanja Stanojevic, Michelle Klingel, et al.
Respiratory Medicine
|
April 22, 2026
Real-World Impact of Elexacaftor/Tezacaftor/Ivacaftor on Health-Related Quality of Life in Adults with Cystic Fibrosis: A 12-Month Multicenter Cohort Study
Razan Kharraz, Elizabeth Tullis, Jenna Sykes, et al.
Chest
|
November 15, 2025
Structural and Functional Pulmonary MRI to Predict Pulmonary Exacerbations in Cystic Fibrosis
Alexander M Matheson, Abdullah S Bdaiwi, Matthew M Willmering, et al.
JAMA
|
May 6, 2010
Effect of azithromycin on pulmonary function in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa: a randomized controlled trial
Lisa Saiman, Michael Anstead, Nicole Mayer-Hamblett, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 17, 2014
Serology as a diagnostic tool for predicting initialPseudomonas aeruginosa acquisition in children with cystic fibrosis
Cori Daines, Donald VanDeVanter, Umer Khan, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
November 5, 2019
Antimicrobial resistance in cystic fibrosis: A Delphi approach to defining best practices
Edith Zemanick, Pierre-Régis Burgel, Giovanni Taccetti, et al.
Pediatric Pulmonology
|
February 3, 2015
Novel outcome measures for clinical trials in cystic fibrosis
Harm A W M Tiddens, Michael Puderbach, Jose G Venegas, et al.
Page
of 33
Search research articles
Search
Showing results (241-250 of 326) with videos related to
Sort By:
Page
of 33
Pediatric Research
|
October 13, 2010
Skeletal muscle metabolism in cystic fibrosis and primary ciliary dyskinesia
Greg D Wells, Donna L Wilkes, Jane E Schneiderman, et al.
Annals of the American Thoracic Society
|
July 10, 2020
Clinical Effectiveness of Lumacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for F508del-CFTR. A Clinical Trial
Scott D Sagel, Umer Khan, Sonya L Heltshe, 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 trial
Harm A W M Tiddens, Yuxin Chen, Eleni-Rosalina Andrinopoulou, et al.
Plos One
|
June 16, 2016
A Systematic Approach to Multiple Breath Nitrogen Washout Test Quality
Renee Jensen, Sanja Stanojevic, Michelle Klingel, et al.
Respiratory Medicine
|
April 22, 2026
Real-World Impact of Elexacaftor/Tezacaftor/Ivacaftor on Health-Related Quality of Life in Adults with Cystic Fibrosis: A 12-Month Multicenter Cohort Study
Razan Kharraz, Elizabeth Tullis, Jenna Sykes, et al.
Chest
|
November 15, 2025
Structural and Functional Pulmonary MRI to Predict Pulmonary Exacerbations in Cystic Fibrosis
Alexander M Matheson, Abdullah S Bdaiwi, Matthew M Willmering, et al.
JAMA
|
May 6, 2010
Effect of azithromycin on pulmonary function in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa: a randomized controlled trial
Lisa Saiman, Michael Anstead, Nicole Mayer-Hamblett, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 17, 2014
Serology as a diagnostic tool for predicting initialPseudomonas aeruginosa acquisition in children with cystic fibrosis
Cori Daines, Donald VanDeVanter, Umer Khan, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
November 5, 2019
Antimicrobial resistance in cystic fibrosis: A Delphi approach to defining best practices
Edith Zemanick, Pierre-Régis Burgel, Giovanni Taccetti, et al.
Pediatric Pulmonology
|
February 3, 2015
Novel outcome measures for clinical trials in cystic fibrosis
Harm A W M Tiddens, Michael Puderbach, Jose G Venegas, et al.
Page
of 33