Nebulised amiloride in respiratory exacerbations of cystic fibrosis: a randomised controlled trial.

Author:

Bowler I M,Kelman B,Worthington D,Littlewood J M,Watson A,Conway S P,Smye S W,James S L,Sheldon T A

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference16 articles.

1. Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation. J7 Clin Invest;Boucher, R.C.; Stutts, M.J.; Knowles, M.R.; Cantley, L.; Gatzy, J.T.,1986

2. Evidence for reduced Clpermeability and increased Na+ permeability in cystic fibrosis human primary cell cultures;Boucher, R.C.; Cotton, C.U.; Gatzy, J.T.; Knowles, M.R.; Yankaskas, JR;JPhysiol (Lond),1988

3. Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis;Knowles, M.R.; Gatzy, J.T.; Boucher, R.C.;NEnglJMed,1981

4. Inhalation of amiloride improves mucociliary and cough clearance in patients with cystic fibrosis;Kohler, D.; App, E.; Schmitz-Schumann, M.; Wurtemburger, G.; Matthys, H.;EurJRespirDis,1986

5. Acute and long-term amiloride inhalation in cystic fibrosis lung disease. A rational approach to cystic fibrosis therapy;App, E.; King, M.; Helferieder, R.; K6hler, D.; Matthys, H.;Am Rev Respir Dis,1990

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