Pulmonary evolution of cystic fibrosis patients colonized by Pseudomonas aeruginosa and/or Burkholderia cepacia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s004310050844.pdf
Reference26 articles.
1. Anonymous (1993) United States Cystic Fibrosis Foundation (letter). 18 January
2. Aronoff SC, Quinn FJ, Stern J, RC (1991) Longitudinal serum IgG response to Pseudomonas cepacia surface antigens in cystic fibrosis. Pediatr Pulmonol 11:289–293
3. Bingen EH, Weber M, Derelle J, Brahimi N, Lambert-Zechovsky NY, Vidailhet M, Navarro J, Elion J (1993) Arbitrarily primed polymerase chain reaction as a rapid method to differentiate crossed from independent Pseudomonas cepacia infections in cystic fibrosis patients. J Clin Microbiol 31, 10:2589–2593
4. Chrispin AR, Norman AP (1974) The systematic evaluation of the chest radiograph with cystic fibrosis. Pediatr Radiol 2:101–105
5. Gladman G, Connor PJ, Williams RF, David TJ (1992) Controlled study of Pseudomonas cepacia and Pseudomonas mal-tophilia in cystic fibrosis. Arch Dis Child 67:192–195
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