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Pediatric Pulmonology
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November 15, 2008
Genetic variations in inflammatory mediators influence lung disease progression in cystic fibrosis
Harriet Corvol, Pierre-Yves Boelle, Jacques Brouard, et al.
The European Respiratory Journal
|
December 22, 2019
Normative data for multiple breath washout outcomes in school-aged Caucasian children
Pinelopi Anagnostopoulou, Philipp Latzin, Renee Jensen, et al.
Thorax
|
April 30, 2021
Time to get serious about the detection and monitoring of early lung disease in cystic fibrosis
Katie J Bayfield, Tonia A Douglas, Tim Rosenow, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
January 12, 2023
Effects of elexacaftor/tezacaftor/ivacaftor therapy in children with cystic fibrosis - a comprehensive assessment using lung clearance index, spirometry, and functional and structural lung MRI
Carmen Streibel, Corin C Willers, Orso Pusterla, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
May 27, 2014
European Cystic Fibrosis Society Standards of Care: Best Practice guidelines
Alan R Smyth, Scott C Bell, Snezana Bojcin, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
June 4, 2021
Effect of lumacaftor-ivacaftor on mucociliary clearance and clinical outcomes in cystic fibrosis: Results from the PROSPECT MCC sub-study
Scott H Donaldson, Beth L Laube, Peter Mogayzel, et al.
Pediatric Pulmonology
|
May 24, 2018
Reference equations for the interpretation of forced expiratory and plethysmographic measurements in infants
Zihang Lu, Rachel E Foong, Krzysztof Kowalik, et al.
Journal of Magnetic Resonance Imaging : JMRI
|
September 11, 2024
Same-Day Repeatability and 28-Day Reproducibility of Xenon MRI Ventilation in Children With Cystic Fibrosis in a Multi-Site Trial
Laura L Walkup, David J Roach, Joseph W Plummer, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
May 28, 2023
Automatic bronchus and artery analysis on chest computed tomography to evaluate the effect of inhaled hypertonic saline in children aged 3-6 years with cystic fibrosis in a randomized clinical trial
Yuxin Chen, Qianting Lv, Eleni-Rosalina Andrinopoulou, et al.
Journal of Clinical Medicine
|
December 9, 2023
Reply to Eker et al. Comment on "Kilian et al. Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. <i>J. Clin. Med.</i> 2023, <i>12</i>, 2704"
Alexandra Kilian, Giuseppe A Latino, Andrew J White, et al.
Page
of 33
Search research articles
Search
Showing results (261-270 of 326) with videos related to
Sort By:
Page
of 33
Pediatric Pulmonology
|
November 15, 2008
Genetic variations in inflammatory mediators influence lung disease progression in cystic fibrosis
Harriet Corvol, Pierre-Yves Boelle, Jacques Brouard, et al.
The European Respiratory Journal
|
December 22, 2019
Normative data for multiple breath washout outcomes in school-aged Caucasian children
Pinelopi Anagnostopoulou, Philipp Latzin, Renee Jensen, et al.
Thorax
|
April 30, 2021
Time to get serious about the detection and monitoring of early lung disease in cystic fibrosis
Katie J Bayfield, Tonia A Douglas, Tim Rosenow, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
January 12, 2023
Effects of elexacaftor/tezacaftor/ivacaftor therapy in children with cystic fibrosis - a comprehensive assessment using lung clearance index, spirometry, and functional and structural lung MRI
Carmen Streibel, Corin C Willers, Orso Pusterla, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
May 27, 2014
European Cystic Fibrosis Society Standards of Care: Best Practice guidelines
Alan R Smyth, Scott C Bell, Snezana Bojcin, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
June 4, 2021
Effect of lumacaftor-ivacaftor on mucociliary clearance and clinical outcomes in cystic fibrosis: Results from the PROSPECT MCC sub-study
Scott H Donaldson, Beth L Laube, Peter Mogayzel, et al.
Pediatric Pulmonology
|
May 24, 2018
Reference equations for the interpretation of forced expiratory and plethysmographic measurements in infants
Zihang Lu, Rachel E Foong, Krzysztof Kowalik, et al.
Journal of Magnetic Resonance Imaging : JMRI
|
September 11, 2024
Same-Day Repeatability and 28-Day Reproducibility of Xenon MRI Ventilation in Children With Cystic Fibrosis in a Multi-Site Trial
Laura L Walkup, David J Roach, Joseph W Plummer, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
May 28, 2023
Automatic bronchus and artery analysis on chest computed tomography to evaluate the effect of inhaled hypertonic saline in children aged 3-6 years with cystic fibrosis in a randomized clinical trial
Yuxin Chen, Qianting Lv, Eleni-Rosalina Andrinopoulou, et al.
Journal of Clinical Medicine
|
December 9, 2023
Reply to Eker et al. Comment on "Kilian et al. Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. <i>J. Clin. Med.</i> 2023, <i>12</i>, 2704"
Alexandra Kilian, Giuseppe A Latino, Andrew J White, et al.
Page
of 33