Tracking CF disease progression with CT and respiratory symptoms in a cohort of children aged 6-19 years-Reference-Cited by-同舟云学术

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Tracking CF disease progression with CT and respiratory symptoms in a cohort of children aged 6-19 years

Published:2014-02-12 Issue:12 Volume:49 Page:1182-1189
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatr Pulmonol.

Author:

Tepper Leonie A.¹²,Caudri Daan¹,Utens Elisabeth M.W.J.³,van der Wiel Els C.¹²,Quittner Alexandra L.⁴,Tiddens Harm A.W.M.¹²

Affiliation:

1. Department of Pediatric Pulmonology; Erasmus Medical Centre-Sophia Children's Hospital; Rotterdam The Netherlands

2. Department of Radiology; Erasmus MC; Rotterdam The Netherlands

3. Department of Child and Adolescent Psychiatry/Psychology; Erasmus MC; Rotterdam The Netherlands

4. Departments of Psychology and Pediatrics; University of Miami; Coral Gables Florida

Funder

Gilead Sciences

Publisher

Wiley

Subject

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

Reference31 articles.

1. Endpoints for clinical trials in young children with cystic fibrosis;Davis;Proc Am Thorac Soc,2007

2. An overview of endpoints for cystic fibrosis clinical trials: one size does not fit all;Rosenfeld;Proc Am Thorac Soc,2007

3. Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis;de Jong;Eur Respir J,2004

4. Chest computed tomography scans should be considered as a routine investigation in cystic fibrosis;Tiddens;Paediatr Respir Rev,2006

5. Lung Clearance Index and HRCT are complementary markers of lung abnormalities in young children with CF;Owens;Thorax,2011

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