Structural lung changes, lung function and non-invasive inflammatory markers in cystic fibrosis

Autor: Robroeks, C.M., Roozeboom, M.H., de Jong, P.A., Tiddens, H.A., Jöbsis, Q., Hendriks, J.J.E., Yntema, J.B., Brackel, H.L., van Gent, R., Robben, S., Dompeling, E.D.

Publikováno v: Pediatric Allergy and Immunology, 21, 493-500. Blackwell Publishing
Pediatric Allergy and Immunology, 21, 3, pp. 493-500
Pediatric Allergy and Immunology, 21, 493-500
Pediatric Allergy and Immunology, 21(3), 493-500. Wiley

Contains fulltext : 89139.pdf (Publisher’s version ) (Closed access) Cystic fibrosis (CF) lung disease is characterized by chronic airway inflammation and recurrent infections, resulting in (ir)reversible structural lung changes and a progressive d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3b45fc9d76b3bdfb614bc54153d11432
https://pure.eur.nl/en/publications/d0709bfa-9d6c-4844-882a-254d4d1dcd11