Nebulized and oral thiol derivatives for pulmonary disease in cystic fibrosis

Author:

Tam Julian1,Nash Edward F2,Ratjen Felix3,Tullis Elizabeth4,Stephenson Anne4

Affiliation:

1. University of Saskatchewan; Division of Respirology, Critical Care, and Sleep Medicine. Department of Medicine; 5th Floor Ellis Hall 103 Hospital Drive Saskatoon SK Canada S7N 0W8

2. Birmingham Heartlands Hospital; Department of Respiratory Medicine; Bordesley Green East Birmingham UK B9 5SS

3. The Hospital for Sick Children; Department of Pediatrics; 555 University Avenue Toronto ON Canada M5G 1XB

4. St Michael's Hospital; Division of Respirology; Toronto ON Canada M5B 1W8

Publisher

Wiley

Subject

Pharmacology (medical)

Reference56 articles.

1. A pilot study of the effect of inhaled buffered reduced glutathione on the clinical status of patients with cystic fibrosis;Bishop;Chest,2005

2. The management of cystic fibrosis with carbocysteine lysine salt: single-blind comparative study with ambroxol hydrochloride;Caramia;The Journal of International Medical Research,1995

3. A phase II study on safety and efficacy of high-dose N-acetylcysteine in patients with cystic fibrosis;Dauletbaev;European Journal of Medical Research,2009

4. A double-blind study of the use of acetylcysteine in patients with cystic fibrosis;Howatt;University of Michigan Medical Center Journal,1966

5. Controlled trial of oral N-acetylcysteine in cystic fibrosis;Mitchell;Australian Paediatric Journal,1982

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