Improved air trapping evaluation in chest computed tomography in children with cystic fibrosis using real-time spirometric monitoring and biofeedback-Reference-Cited by-同舟云学术

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Improved air trapping evaluation in chest computed tomography in children with cystic fibrosis using real-time spirometric monitoring and biofeedback

Published:2013-12 Issue:6 Volume:12 Page:559-566
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Kongstad Thomas,Buchvald Frederik F.,Green Kent,Lindblad Anders,Robinson Terry E.,Nielsen Kim G.

Funder

John & Birthe Meyer Foundation

Toyota Foundation

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Reference33 articles.

1. Computed tomography in the evaluation of cystic fibrosis lung disease;Brody;Am J Respir Crit Care Med,2005

2. Cystic fibrosis lung disease: genetic influences, microbial interactions, and radiological assessment;Moskowitz;Pediatr Radiol,2005

3. Progression of lung disease on computed tomography and pulmonary function tests in children and adults with cystic fibrosis;de Jong;Thorax,2006

4. Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosis;Davis;Am J Respir Crit Care Med,2007

5. Cystic fibrosis HRCT scores correlate strongly with Pseudomonas infection;Robinson;Pediatr Pulmonol,2009

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1. Comparative sensitivity of early cystic fibrosis lung disease detection tools in school aged children;Journal of Cystic Fibrosis;2024-07

2. Comparative sensitivity of Early Cystic Fibrosis Lung Disease detection tools in school aged children;2023-11-07

3. Implementation and evaluation of ultra-low dose CT in early cystic fibrosis lung disease;European Respiratory Journal;2023-06-29

4. Chronic airway disease in primary ciliary dyskinesia—spiced with geno–phenotype associations;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2022-03

5. A Short extension to multiple breath washout provides additional signal of distal airway disease in people with CF: A pilot study;Journal of Cystic Fibrosis;2022-01

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