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The European Respiratory Journal
|
November 5, 2002
Measurements of interrupter resistance: reference values for children 3-13 yrs of age
P J F M Merkus, H G M Arets, T Joosten, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
April 22, 2011
Assessment of CFTR function in homozygous R117H-7T subjects
R A de Nooijer, J M Nobel, H G M Arets, et al.
Medicine and Science in Sports and Exercise
|
May 23, 2014
Prediction of mortality in adolescents with cystic fibrosis
Erik H J Hulzebos, Hanna Bomhof-Roordink, Pauline B van de Weert-van Leeuwen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 10, 2013
Lung clearance index: evidence for use in clinical trials in cystic fibrosis
L Kent, P Reix, J A Innes, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
January 12, 2020
Clinical effect of lumacaftor/ivacaftor in F508del homozygous CF patients with FEV<sub>1</sub> ≥ 90% predicted at baseline
B L Aalbers, K M de Winter-de Groot, H G M Arets, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
May 26, 2020
Females with cystic fibrosis have a larger decrease in sweat chloride in response to lumacaftor/ivacaftor compared to males
B L Aalbers, R W Hofland, I Bronsveld, et al.
Microbiology Spectrum
|
May 18, 2023
16S rRNA-Based Microbiota Profiling Assists Conventional Culture Analysis of Airway Samples from Pediatric Cystic Fibrosis Patients
Maartje Kristensen, Emma M de Koff, Mei Ling Chu, et al.
Annals of the American Thoracic Society
|
April 24, 2013
An official American Thoracic Society workshop report: optimal lung function tests for monitoring cystic fibrosis, bronchopulmonary dysplasia, and recurrent wheezing in children less than 6 years of age
Margaret Rosenfeld, Julian Allen, Bert H G M Arets, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
The European Respiratory Journal
|
November 5, 2002
Measurements of interrupter resistance: reference values for children 3-13 yrs of age
P J F M Merkus, H G M Arets, T Joosten, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
April 22, 2011
Assessment of CFTR function in homozygous R117H-7T subjects
R A de Nooijer, J M Nobel, H G M Arets, et al.
Medicine and Science in Sports and Exercise
|
May 23, 2014
Prediction of mortality in adolescents with cystic fibrosis
Erik H J Hulzebos, Hanna Bomhof-Roordink, Pauline B van de Weert-van Leeuwen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 10, 2013
Lung clearance index: evidence for use in clinical trials in cystic fibrosis
L Kent, P Reix, J A Innes, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
January 12, 2020
Clinical effect of lumacaftor/ivacaftor in F508del homozygous CF patients with FEV<sub>1</sub> ≥ 90% predicted at baseline
B L Aalbers, K M de Winter-de Groot, H G M Arets, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
May 26, 2020
Females with cystic fibrosis have a larger decrease in sweat chloride in response to lumacaftor/ivacaftor compared to males
B L Aalbers, R W Hofland, I Bronsveld, et al.
Microbiology Spectrum
|
May 18, 2023
16S rRNA-Based Microbiota Profiling Assists Conventional Culture Analysis of Airway Samples from Pediatric Cystic Fibrosis Patients
Maartje Kristensen, Emma M de Koff, Mei Ling Chu, et al.
Annals of the American Thoracic Society
|
April 24, 2013
An official American Thoracic Society workshop report: optimal lung function tests for monitoring cystic fibrosis, bronchopulmonary dysplasia, and recurrent wheezing in children less than 6 years of age
Margaret Rosenfeld, Julian Allen, Bert H G M Arets, et al.
Page
of 3