A screening tool to identify risk for bronchiectasis progression in children with cystic fibrosis-Reference-Cited by-同舟云学术

A screening tool to identify risk for bronchiectasis progression in children with cystic fibrosis

Published:2021-10-12 Issue:1 Volume:57 Page:122-131
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatric Pulmonology

Author:

Caudri Daan¹²³^ORCID,Turkovic Lidija¹,Klerk Nicholas H.¹,Rosenow Tim¹^ORCID,Murray Conor P.⁴,Steyerberg Ewout W.⁵⁶,Ranganathan Sarath C.⁷⁸⁹,Sly Peter¹⁰^ORCID,Stick Stephen M.¹²,Breuer Oded¹²¹¹^ORCID,

Affiliation:

1. Telethon Kids Institute The University of Western Australia Perth Australia

2. Department of Respiratory Medicine Princess Margaret Hospital Perth Australia

3. Department of Pediatrics/Respiratory Medicine Erasmus MC Rotterdam The Netherlands

4. Department of Diagnostic Imaging Princess Margaret Hospital for Children Perth Western Australia Australia

5. Department of Public Health Erasmus MC Rotterdam The Netherlands

6. Department of Medical Statistics and Bioinformatics Leiden University Medical Center Leiden The Netherlands

7. Murdoch Children's Research Institute Parkville Australia

8. Department of Respiratory Medicine Royal Children's Hospital Parkville Australia

9. Department of Paediatrics University of Melbourne Parkville Australia

10. Child Health Research Centre The University of Queensland Brisbane Australia

11. Pediatric Pulmonology and CF Unit, Department of Pediatrics Hadassah‐Hebrew University Medical Center Jerusalem Israel

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ppul.25712

Reference35 articles.

1. Cystic fibrosis lung inflammation: early, sustained, and severe;Cantin A;Am J Respir Crit Care Med,1995

2. Genetic Variation and Clinical Heterogeneity in Cystic Fibrosis

3. Predicting disease progression in cystic fibrosis

4. Pulmonary outcome prediction (POP) tools for cystic fibrosis patients

5. Early detection of cystic fibrosis lung disease: multiple-breath washout versus raised volume tests

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