Inhaled antibiotic therapy in non-cystic fibrosis patients with bronchiectasis and chronic bronchial infection by Pseudomonas aeruginosa
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine
Reference29 articles.
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2. Mucoid Pseudomonas aeruginosa is a marker of poor survival in cystic fibrosis;Henry;Pediatr Pulmonol,1992
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4. Inhaled antibiotics in cystic fibrosis;Wall;Lancet,1983
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