Prospective longitudinal association between repeated multiple breath washout measurements and computed tomography scores in children with cystic fibrosis-Reference-Cited by-同舟云学术

Prospective longitudinal association between repeated multiple breath washout measurements and computed tomography scores in children with cystic fibrosis

Published:2021-07 Issue:4 Volume:20 Page:632-640
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Sandvik Rikke Mulvad,Kongstad Thomas,Green Kent,Voldby Christian^ORCID,Buchvald Frederik,Skov Marianne,Pressler Tacjana,Nielsen Kim Gjerum^ORCID

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Reference33 articles.

1. Cystic fibrosis;Davis;Am J Respir Crit Care Med,1996

2. Chest computed tomography scores are predictive of survival in patients with cystic fibrosis awaiting lung transplantation;Loeve;Am J Respir Crit Care Med,2012

3. PRAGMA-CF. A quantitative structural lung disease computed tomography outcome in young children with cystic fibrosis;Rosenow;Am J Respir Crit Care Med,2015

4. The cumulative effect of inflammation and infection on structural lung disease in early cystic fibrosis;Rosenow;Eur Respir J,2019

5. Risk factors for progression of structural lung disease in school-age children with cystic fibrosis;Svedberg;J Cyst Fibros,2019

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Impact of Reanalysis of Nitrogen Multiple-Breath Washout on its Relationship with Chest Magnetic Resonance Imaging Findings in Clinically Stable and Pulmonary Exacerbated Children with Cystic Fibrosis;Klinische Pädiatrie;2023-12-18

2. Automatic analysis of bronchus-artery dimensions to diagnose and monitor airways disease in cystic fibrosis;Thorax;2023-09-21

3. 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;Journal of Cystic Fibrosis;2023-09

4. Nationwide lung function monitoring from infancy in newborn-screened children with cystic fibrosis;ERJ Open Research;2023-08-17

5. The clinical impact of Lumacaftor-Ivacaftor on structural lung disease and lung function in children aged 6–11 with cystic fibrosis in a real-world setting;Respiratory Research;2023-08-11