Elsevier

The Lancet

Volume 341, Issue 8852, 24 April 1993, Pages 1070-1074
The Lancet

SCIENCE & PRACTICE
Clinical management of pulmonary disease in cystic fibrosis

https://doi.org/10.1016/0140-6736(93)92423-QGet rights and content

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References (47)

  • M. Spector et al.

    Pneumothorax in cystic fibrosis: a 26-year experience

    Ann Thorac Surg

    (1989)
  • Be Noyes et al.

    Treatment of pneumothorax in cystic fibrosis in the era of lung transplantation

    Chest

    (1992)
  • A. Coates

    Oxygen therapy, exercise, and cystic fibrosis

    Chest

    (1992)
  • R. Zinman et al.

    Nocturnal home oxygen in the treatment of hypoxemic cystic fibrosis patients

    J Pediatr

    (1989)
  • M. Konstan et al.

    Ibuprofen in children with cystic fibrosis: pharmacokinetics and adverse effects

    J Pediatr

    (1991)
  • N. McElvaney et al.

    Aerosol alpha-1-antitrypsin treatment for cystic fibrosis

    Lancet

    (1991)
  • C. Falliers

    Controlled study of iodotherapy for childhood asthma

    J Allergy

    (1966)
  • T. Petty

    The national mucolytic study: results of a randomized, double-blind, placebo-controlled study of iodinated glycerol in chronic obstructive bronchitis

    Chest

    (1990)
  • Gb Winnie et al.

    Intravenous immune globulin treatment of pulmonary exacerbations in cystic fibrosis

    J Pediatr

    (1989)
  • L. Hjelte et al.

    Prospective study of mycobacterial infections in patients with cystic fibrosis

    Thorax

    (1990)
  • Cg Prober

    The impact of respiratory viral infections in patients with CF

    Clin Rev Allergy

    (1991)
  • J. Bosso

    Advances in the pharmacotherapy of cystic fibrosis

    J Clin Pharm Ther

    (1992)
  • K. Kerrebijn et al.

    Pulmonary infection and antibiotic treatment in cystic fibrosis

    Chest

    (1988)
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