Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Editorial
. 2013 Dec;31(4):418-9.
doi: 10.1590/S0103-05822013000400001.

Dornase alpha use in patients with cystic fibrosis

[Article in English, Portuguese]
Affiliations
Editorial

Dornase alpha use in patients with cystic fibrosis

[Article in English, Portuguese]
Paulo José C Marostica. Rev Paul Pediatr. 2013 Dec.
No abstract available

PubMed Disclaimer

Conflict of interest statement

Conflito de interesse: nada a declarar

Comment on

References

    1. Raskin S, Pereira-Ferrari L, Reis FC, Abreu F, Marostica P, Rozov T, et al. Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients. J Cyst Fibros. 2008;7:15–22. - PubMed
    1. Chernick WS, Barbero GJ. Composition of tracheobronchial secretions in cystic fibrosis of the pancreas and bronchiectasis. Pediatrics. 1959;24:739–745. - PubMed
    1. Fuchs HJ, Borowitz DS, Christiansen DH, Morris EM, Nash M, Ramsey BW, et al. Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study Group. N Engl J Med. 1994;331:637–642. - PubMed
    1. Amin R, Subbarao P, Lou W, Jabar A, Balkovec S, Jensen R, et al. The effect of dornase alfa on ventilation inhomogeneity in patients with cystic fibrosis. Eur Respir J. 2011;37:806–812. - PubMed
    1. Robinson TE, Goris ML, Zhu HJ, Chen X, Bhise P, Sheikh F, et al. Dornase alfa reduces air trapping in children with mild cystic fibrosis lung disease: a quantitative analysis. Chest. 2005;128:2327–2335. - PubMed

MeSH terms