| scholarly article | Q13442814 |
| P2093 | author name string | Taylor CJ | |
| Duerden BI | |||
| Baxter PS | |||
| McGaw J | |||
| Howden R | |||
| P2860 | cites work | Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation | Q30449378 |
| Role of adherence in the pathogenesis of Pseudomonas aeruginosa lung infection in cystic fibrosis patients | Q33911265 | ||
| Bacterial contamination of home nebuliser | Q34072501 | ||
| THE POTENTIAL ROLE OF INHALATION THERAPY EQUIPMENT IN NOSOCOMIAL PULMONARY INFECTION | Q34078948 | ||
| Selective decontamination | Q44197837 | ||
| The pathogenicity of Haemophilus influenzae. | Q53775934 | ||
| Pseudomonas aeruginosa in the oral cavity and sputum of patients with cystic fibrosis. | Q54449202 | ||
| SPACED ADMINISTRATION OF ANTIBIOTIC COMBINATIONS TO ELIMINATE PSEUDOMONAS FROM SPUTUM IN CYSTIC FIBROSIS | Q60531077 | ||
| Nebulizer contamination in a burn unit | Q69499559 | ||
| Microbial contamination of domiciliary nebuliser therapy equipment | Q69853793 | ||
| Nebulised colomycin for early pseudomonas colonisation in cystic fibrosis | Q69859518 | ||
| Serratia marcescens Infections from Inhalation Therapy Medications: Nosocomial Outbreak | Q69912311 | ||
| A new medium for the isolation of Staphylococcus aureus, including thymine requiring strains, from sputum | Q70883184 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cystic fibrosis | Q178194 |
| P304 | page(s) | 175-177 | |
| P577 | publication date | 1990-02-01 | |
| P1433 | published in | Archives of Disease in Childhood | Q4787296 |
| P1476 | title | Bacterial reservoirs in cystic fibrosis | |
| P478 | volume | 65 |
| Q35800789 | A case of failed eradication of cystic fibrosis-related sinus colonisation by Pseudomonas aeruginosa |
| Q38769187 | Acquisition and adaptation of the airway microbiota in the early life of cystic fibrosis patients |
| Q33883196 | Alpha-AP-2 directs myosin VI-dependent endocytosis of cystic fibrosis transmembrane conductance regulator chloride channels in the intestine |
| Q33734772 | Bronchiectasis in Children: Current Concepts in Immunology and Microbiology |
| Q57838884 | COMPLEMENTARY ROLE OF MR IMAGING OF ETHMOMAXILLARY SINUS DISEASE DEPICTED AT CT IN CYSTIC FIBROSIS |
| Q39218303 | Clinical implications of Pseudomonas aeruginosa location in the lungs of patients with cystic fibrosis |
| Q35563535 | Epidemiology of chronic Pseudomonas aeruginosa infections in the airways of lung transplant recipients with cystic fibrosis |
| Q36263103 | Extrapulmonary sites of Pseudomonas aeruginosa in adults with cystic fibrosis |
| Q37624582 | New insights into the pathogenesis of cystic fibrosis sinusitis |
| Q35607468 | Pseudomonas aeruginosa and Periodontal Pathogens in the Oral Cavity and Lungs of Cystic Fibrosis Patients: a Case-Control Study |
| Q38599404 | Sinus bacteriology in patients with cystic fibrosis or primary ciliary dyskinesia: A systematic review |
| Q38130897 | Staphylococcus aureus in early cystic fibrosis lung disease |
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