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Proceedings of the National Academy of Sciences of the United States of America
|
May 27, 2026
Multiple defects in macrophage antibacterial responses support intracellular survival of <i><i>Mycobacterium</i> abscessus</i> in cystic fibrosis
Abdullah A Tarique, Stefan Emming, Dean Kelk, et al.
Clinical Chemistry
|
August 19, 2007
Novel neutrophil-derived proteins in bronchoalveolar lavage fluid indicate an exaggerated inflammatory response in pediatric cystic fibrosis patients
Brendan J McMorran, Severine A Ouvry Patat, John B Carlin, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 12, 2025
Infection by Clonally Related <i>Mycobacterium abscessus</i> Isolates: The Role of Drinking Water
Rachel M Thomson, Nicole Wheeler, Rebecca E Stockwell, et al.
The Lancet. Respiratory Medicine
|
December 23, 2021
Efficacy and safety of elexacaftor plus tezacaftor plus ivacaftor versus tezacaftor plus ivacaftor in people with cystic fibrosis homozygous for F508del-CFTR: a 24-week, multicentre, randomised, double-blind, active-controlled, phase 3b trial
Sivagurunathan Sutharsan, Edward F McKone, Damian G Downey, et al.
The New England Journal of Medicine
|
November 4, 2011
A CFTR potentiator in patients with cystic fibrosis and the G551D mutation
Bonnie W Ramsey, Jane Davies, N Gerard McElvaney, et al.
Thorax
|
January 28, 2021
Assessing the impact of the 13 valent pneumococcal vaccine on childhood empyema in Australia
Roxanne Strachan, Nusrat Homaira, Sean Beggs, et al.
The New England Journal of Medicine
|
May 19, 2015
Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR
Claire E Wainwright, J Stuart Elborn, Bonnie W Ramsey, et al.
The Lancet. Respiratory Medicine
|
February 13, 2021
Long-term safety and efficacy of tezacaftor-ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND): an open-label extension study
Patrick A Flume, Reta Fischer Biner, Damian G Downey, et al.
Annals of the American Thoracic Society
|
September 8, 2025
Evaluating Long-Term Effectiveness of Cystic Fibrosis Modulator Therapies After Rapid Adoption: A Dual-Approach Study
Pedro Miranda Afonso, Grace C Zhou, Weiji Su, et al.
Pediatric Pulmonology
|
September 10, 2008
Safety of bronchoalveolar lavage in young children with cystic fibrosis
Claire E Wainwright, Keith Grimwood, John B Carlin, et al.
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Search research articles
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Showing results (81-90 of 96) with videos related to
Sort By:
Page
of 10
Proceedings of the National Academy of Sciences of the United States of America
|
May 27, 2026
Multiple defects in macrophage antibacterial responses support intracellular survival of <i><i>Mycobacterium</i> abscessus</i> in cystic fibrosis
Abdullah A Tarique, Stefan Emming, Dean Kelk, et al.
Clinical Chemistry
|
August 19, 2007
Novel neutrophil-derived proteins in bronchoalveolar lavage fluid indicate an exaggerated inflammatory response in pediatric cystic fibrosis patients
Brendan J McMorran, Severine A Ouvry Patat, John B Carlin, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 12, 2025
Infection by Clonally Related <i>Mycobacterium abscessus</i> Isolates: The Role of Drinking Water
Rachel M Thomson, Nicole Wheeler, Rebecca E Stockwell, et al.
The Lancet. Respiratory Medicine
|
December 23, 2021
Efficacy and safety of elexacaftor plus tezacaftor plus ivacaftor versus tezacaftor plus ivacaftor in people with cystic fibrosis homozygous for F508del-CFTR: a 24-week, multicentre, randomised, double-blind, active-controlled, phase 3b trial
Sivagurunathan Sutharsan, Edward F McKone, Damian G Downey, et al.
The New England Journal of Medicine
|
November 4, 2011
A CFTR potentiator in patients with cystic fibrosis and the G551D mutation
Bonnie W Ramsey, Jane Davies, N Gerard McElvaney, et al.
Thorax
|
January 28, 2021
Assessing the impact of the 13 valent pneumococcal vaccine on childhood empyema in Australia
Roxanne Strachan, Nusrat Homaira, Sean Beggs, et al.
The New England Journal of Medicine
|
May 19, 2015
Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR
Claire E Wainwright, J Stuart Elborn, Bonnie W Ramsey, et al.
The Lancet. Respiratory Medicine
|
February 13, 2021
Long-term safety and efficacy of tezacaftor-ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND): an open-label extension study
Patrick A Flume, Reta Fischer Biner, Damian G Downey, et al.
Annals of the American Thoracic Society
|
September 8, 2025
Evaluating Long-Term Effectiveness of Cystic Fibrosis Modulator Therapies After Rapid Adoption: A Dual-Approach Study
Pedro Miranda Afonso, Grace C Zhou, Weiji Su, et al.
Pediatric Pulmonology
|
September 10, 2008
Safety of bronchoalveolar lavage in young children with cystic fibrosis
Claire E Wainwright, Keith Grimwood, John B Carlin, et al.
Page
of 10