Mucus plugging, air trapping, and bronchiectasis are important outcome measures in assessing progressive childhood cystic fibrosis lung disease-Reference-Cited by-同舟云学术

Mucus plugging, air trapping, and bronchiectasis are important outcome measures in assessing progressive childhood cystic fibrosis lung disease

Published:2020-01-21 Issue:4 Volume:55 Page:929-938
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatr Pulmonol

Author:

Robinson Terry E.¹^ORCID,Goris Michael L.²,Moss Richard B.¹,Tian Lu³,Kan Peiyi⁴,Yilma Mignote¹,McCoy Karen S.⁵,Newman Beverley⁶,Jong Pim A.⁷,Long Frederick R.⁸,Brody Alan S.⁹,Behrje Rhett¹⁰,Yates Denise P.¹¹,Cornfield David N.¹

Affiliation:

1. Department of Pediatrics, Center of Excellence in Pulmonary Biology Stanford University School of Medicine Stanford California

2. Division of Nuclear Medicine/Radiology Stanford University School of Medicine Stanford California

3. Department of Biomedical Data Science Stanford University School of Medicine Stanford California

4. Department of Pediatrics Research and Statistical Unit Stanford University School of Medicine Stanford California

5. Division of Pulmonary Medicine, Department of Pediatrics Nationwide Children's Hospital Columbus Ohio

6. Department of Radiology Stanford University School of Medicine Stanford California

7. Department of Radiology University Medical Center Utrecht The Netherlands

8. Department of Radiology Nationwide Children's Hospital Columbus Ohio

9. Department of Radiology Cincinnati Children's Hospital Cincinnati Ohio

10. Department of Global Development Takeda Pharmaceuticals Cambridge Massachusetts

11. Department of Biomarker Development Novartis Institutes for BioMedical Research Cambridge Massachusetts

Funder

Novartis Institutes for Biomedical Research, Cambridge, MA, USA

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ppul.24646

Reference26 articles.

1. PRAGMA-CF. A Quantitative Structural Lung Disease Computed Tomography Outcome in Young Children with Cystic Fibrosis

2. Automatic Airway Analysis on Multidetector Computed Tomography in Cystic Fibrosis

3. Objective airway artery dimensions compared to CT scoring methods assessing structural cystic fibrosis lung disease

4. Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification

5. An Automated Approach to Quantitative Air Trapping Measurements in Mild Cystic Fibrosis

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