Risk factors for lung function decline in a large cohort of young cystic fibrosis patients-Reference-Cited by-同舟云学术

Risk factors for lung function decline in a large cohort of young cystic fibrosis patients

Published:2015-06-09 Issue:8 Volume:50 Page:763-770
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatr Pulmonol.

Author:

Cogen Jonathan¹,Emerson Julia¹,Sanders Don B.²,Ren Clement³,Schechter Michael S.⁴,Gibson Ronald L.¹,Morgan Wayne⁵,Rosenfeld Margaret¹,

Affiliation:

1. Division of Pulmonary Medicine; Department of Pediatrics; University of Washington; Seattle Washington

2. Department of Pediatrics; American Family Children's Hospital; Madison Wisconsin

3. Division of Pediatric Pulmonology; University of Rochester; Rochester New York

4. Division of Pulmonary Medicine; Department of Pediatrics; Virginia Commonwealth University; Children's Hospital of Richmond at VCU; Richmond Virginia

5. Departments of Pediatrics and Physiology; Pediatric Pulmonary Center; University of Arizona; Tucson Arizona

Funder

Cystic Fibrosis Foundation Therapeutics

Nemours Children's Clinic Research Program, Jacksonville, FL

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ppul.23217/fullpdf

Reference31 articles.

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2. Jointly modelling the relationship between survival and pulmonary function in cystic fibrosis patients;Schluchter;Stat Med,2002

3. Effect of high-dose ibuprofen in patients with cystic fibrosis;Konstan;N Engl J Med,1995

4. Relationship between inhaled corticosteroid therapy and rate of lung function decline in children with cystic fibrosis;Ren;J Pediatr,2008

5. Clinical use of dornase alpha is associated with a slower rate of FEV1 decline in cystic fibrosis;Konstan;Pediatr Pulmonol,2011

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