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The Lancet. Respiratory Medicine
|
June 15, 2016
Efficacy and safety of lumacaftor/ivacaftor combination therapy in patients with cystic fibrosis homozygous for Phe508del CFTR by pulmonary function subgroup: a pooled analysis
J Stuart Elborn, Bonnie W Ramsey, Michael P Boyle, et al.
Diagnostic Microbiology and Infectious Disease
|
November 26, 2008
Identification of Pseudomonas aeruginosa by a duplex real-time polymerase chain reaction assay targeting the ecfX and the gyrB genes
Snehal N Anuj, David M Whiley, Timothy J Kidd, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 18, 2025
The changing face of cystic fibrosis research: challenges of multi-centre microbiology cohort studies
Ieuan Es Evans, Christine M Duplancic, Timothy A Kidd, et al.
British Journal of Clinical Pharmacology
|
November 1, 2006
A d-optimal designed population pharmacokinetic study of oral itraconazole in adult cystic fibrosis patients
Stefanie Hennig, Timothy H Waterhouse, Scott C Bell, et al.
Clinical Therapeutics
|
April 24, 2026
Lumacaftor-Ivacaftor in Pediatric Patients With Cystic Fibrosis and Advanced Liver Disease: A Pilot Study
Adeline Y L Lim, Maria P Hernández-Mitre, Peter J Lewindon, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 5, 2018
Differential expression of genes and receptors in monocytes from patients with cystic fibrosis
Abdullah A Tarique, Peter D Sly, Diana G Cardenas, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 5, 2025
Improvements in health-related quality of life in people with cystic fibrosis ≥6 years of age treated with vanzacaftor/tezacaftor/deutivacaftor
Claire E Wainwright, Teja Thorat, Sarah Conner, et al.
Journal of Paediatrics and Child Health
|
July 15, 2005
Pubertal development and its influences on bone mineral density in Australian children and adolescents with cystic fibrosis
Helen M Buntain, Ristan M Greer, Joseph C H Wong, et al.
The Lancet. Respiratory Medicine
|
June 11, 2018
Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a CFTR gating mutation (ARRIVAL): a phase 3 single-arm study
Margaret Rosenfeld, Claire E Wainwright, Mark Higgins, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
August 21, 2025
Validation of an artificial intelligence-based automated PRAGMA and mucus plugging algorithm in pediatric cystic fibrosis
Pranali Raut, Yuxin Chen, Ahmad Taleb, et al.
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Search research articles
Search
Showing results (31-40 of 96) with videos related to
Sort By:
Page
of 10
The Lancet. Respiratory Medicine
|
June 15, 2016
Efficacy and safety of lumacaftor/ivacaftor combination therapy in patients with cystic fibrosis homozygous for Phe508del CFTR by pulmonary function subgroup: a pooled analysis
J Stuart Elborn, Bonnie W Ramsey, Michael P Boyle, et al.
Diagnostic Microbiology and Infectious Disease
|
November 26, 2008
Identification of Pseudomonas aeruginosa by a duplex real-time polymerase chain reaction assay targeting the ecfX and the gyrB genes
Snehal N Anuj, David M Whiley, Timothy J Kidd, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 18, 2025
The changing face of cystic fibrosis research: challenges of multi-centre microbiology cohort studies
Ieuan Es Evans, Christine M Duplancic, Timothy A Kidd, et al.
British Journal of Clinical Pharmacology
|
November 1, 2006
A d-optimal designed population pharmacokinetic study of oral itraconazole in adult cystic fibrosis patients
Stefanie Hennig, Timothy H Waterhouse, Scott C Bell, et al.
Clinical Therapeutics
|
April 24, 2026
Lumacaftor-Ivacaftor in Pediatric Patients With Cystic Fibrosis and Advanced Liver Disease: A Pilot Study
Adeline Y L Lim, Maria P Hernández-Mitre, Peter J Lewindon, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 5, 2018
Differential expression of genes and receptors in monocytes from patients with cystic fibrosis
Abdullah A Tarique, Peter D Sly, Diana G Cardenas, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 5, 2025
Improvements in health-related quality of life in people with cystic fibrosis ≥6 years of age treated with vanzacaftor/tezacaftor/deutivacaftor
Claire E Wainwright, Teja Thorat, Sarah Conner, et al.
Journal of Paediatrics and Child Health
|
July 15, 2005
Pubertal development and its influences on bone mineral density in Australian children and adolescents with cystic fibrosis
Helen M Buntain, Ristan M Greer, Joseph C H Wong, et al.
The Lancet. Respiratory Medicine
|
June 11, 2018
Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a CFTR gating mutation (ARRIVAL): a phase 3 single-arm study
Margaret Rosenfeld, Claire E Wainwright, Mark Higgins, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
August 21, 2025
Validation of an artificial intelligence-based automated PRAGMA and mucus plugging algorithm in pediatric cystic fibrosis
Pranali Raut, Yuxin Chen, Ahmad Taleb, et al.
Page
of 10