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1.
Bosso John A. Efficacy of ciprofloxacin in patients with cystic fibrosis // Drug Intell. and Clin. Pharm., 1988. Vol. 22, N 7-8.-С.551-553

2.
Fibronectin-cleaving activity of bronchial secretions of patients with cystic fibrosis // J. Infec. Diseases, 1988. Vol. 158, N 1.-С.89-100

3.
Genome fingerprinting of Pseudomonas aeruginosa indicates colonization of cystic fibrosis siblings with closely related strains // J. Clin. Microbiol., 1988. Vol. 26, N 10.-С.1973-1977

4.
Thompson Geoffrey N. Taurine uptake by normal and cystic fibrosis fibroblasts // Biochem. and Cell Biol., 1988. Vol. 66, N 7.-С.702-706

5.
Short-term nutritional supplementation during management of pulmonary exacerbations in cystic fibrosis: a controlled study, including effects of protein turnover // Amer. J. Clin. Nutr., 1988. Vol. 48, N 2.-С.235-239

6.
Durand J. Physiologie de l'epithelium tracheal // Arch. int. physiol. et biochim, 1988. Vol. 96, N 4.-С.347-362

7.
Comparative evaluation of selective media for isolation of Pseudomonas cepacia from cystic fibrosis patients and environmental sources // J. Clin. Microbiol., 1988. Vol. 26, N 10.-С.2096-2100

8.
Rectum has abnormal ion transport but normal cAMP-binding proteins in cystic fibrosis // Amer. J. Physiol., 1988. Vol. 254, N 5.-С.С719-С724

9.
Brautigan David L. Molecular defects in ion channel regulation in cystic fibrosis predicted from analysis of protein phosphorylation/dephosphorilation // Int. J. Biechem., 1988. Vol. 20, N 8.-С.745-752

10.
Impaired chloride secretion, as well as bicarbonate secretion, underlies the fluid secretory defect in the cystic fibrosis pancreas // Gastroenterology, 1988. Vol. 95, N 2.-С.349-355

11.
Pier Gerald B. Polysaccharide antigens of Pseudomonas aeruginosa // Rev. Infec. Diseases, 1988. Vol. 10, N 2.-С.337-340

12.
Gilleland H.E. Adaptive alterations in the outer membrane of gram-negative bacteria during human infection // Can. J. Microbiol., 1988. Vol. 34, N 4.-С.499-502

13.
Karbocystein - ucinne mukolytikum pri cystickej fibroze pluc // Cs. pediat., 1988. Vol. 43, N 10.-С.602-664

14.
Longitudinal study of antibody response to lipopolysaccharides during chronic Pseudomonas aeruginosa lung infection in cystic fibrosis // Infec. and Immun., 1988. Vol. 56, N 9.-С.2270-2278

15.
Gordon C.A. Antibiotic interaction and diffusion through alginate and exopolysaccharide of cystic fibrosis-derived Pseudomonas aeruginosa // J. Antimicrob. Chemother., 1988. Vol. 22, N 5.-С.667-674

16.
Visual and somatosensory evoked potentials in vitamin E deficiency with cystic fibrosis // Electroencephalogr. and Clin. Neurophysiol., 1988. Vol. 71, N 4.-С.266-272

17.
Unusual clastering of allergic bronchopulmonary aspergillosis in children with cystic fibrosis // Pediatrics, 1988. Vol. 82, N 6.-С.835-839

18.
Antibiotici anti-Pseudomonas in fibrosi cistica: studio microbiologico // Gaslini, 1988. Vol. 20, N 2.-С.208-214

19.
Effects of five antibiotics on adhesion and haemagglutinating properties of Pseudomonas aeruginosa isolated from cystic fibrosis patients // Drugs Exp. and Clin. Res., 1988. Vol. 14, N 10.-С.635-643

20.
Aronoff Stephen C. Outer membrane permeability in Pseudomonas cepacia: diminished porin content in a 'бета'-lactam-resistant mutant and in resistant cystic fibrosis isolates // Antimicrob. Agents and Chemother., 1988. Vol. 32, N 11.-С.1636-1639

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