| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Zach MS | |
| P2860 | cites work | Production of mucoid microcolonies by Pseudomonas aeruginosa within infected lungs in cystic fibrosis | Q33903005 |
| Role of pili in adherence of Pseudomonas aeruginosa to mammalian buccal epithelial cells | Q33908183 | ||
| Role of adherence in the pathogenesis of Pseudomonas aeruginosa lung infection in cystic fibrosis patients | Q33911265 | ||
| Mucociliary transport in trachea of patients with cystic fibrosis | Q34988624 | ||
| Prospective, controlled study of a polyvalent pseudomonas vaccine in cystic fibrosis--three year results | Q35118667 | ||
| Reversible airway obstruction in cystic fibrosis | Q36465230 | ||
| Pulmonary changes and cor pulmonale in mucoviscidosis | Q36478998 | ||
| Effect of ciliostatic factors from Pseudomonas aeruginosa on rabbit respiratory cilia | Q37030786 | ||
| Rigidity of tracheae and bronchi during muscular constriction | Q72227916 | ||
| The systematic evaluation of the chest radiograph in cystic fibrosis | Q81635886 | ||
| A longitudinal study of bronchodilator responsiveness in cystic fibrosis | Q93566031 | ||
| Role of Pseudomonas aeruginosa mucoid exopolysaccharide in adherence to tracheal cells | Q37038466 | ||
| Role of pili in the adherence of Pseudomonas aeruginosa to injured tracheal epithelium | Q37080823 | ||
| Adherence of mucoid and nonmucoid Pseudomonas aeruginosa to acid-injured tracheal epithelium | Q37109863 | ||
| Lung disease in cystic fibrosis--an updated concept | Q37929015 | ||
| Pathogenesis of the pseudomonas lung lesion in cystic fibrosis | Q38227182 | ||
| The role of immune complexes in the pathogenesis of bacterial infections | Q39480111 | ||
| Bacterial Flora of Respiratory Tract in Patients with Cystic Fibrosis, 1950-1971 | Q39521472 | ||
| Chemistry and biology of the alginate of mucoid strains of Pseudomonas aeruginosa in cystic fibrosis | Q39602315 | ||
| Pulmonary host defense: defects that lead to chronic inflammation of the airway. | Q39609385 | ||
| Proteolytic cleavage of human IgG molecules by neutral proteases of polymorphonuclear leukocytes | Q39633584 | ||
| Antibacterial therapy in cystic fibrosis. A review of the literature published between 1980 and February 1987. | Q39654171 | ||
| Chest physiotherapy--the mechanical approach to antiinfective therapy in cystic fibrosis | Q39686178 | ||
| Imbalance between polymorphonuclear leukocyte proteases and antiproteases in chronic pyogenic infections and its relation to the proteolysis of complement component C3. | Q39740949 | ||
| Adherence of Pseudomonas aeruginosa to tracheal cells injured by influenza infection or by endotracheal intubation. | Q41156798 | ||
| Immunologic investigations of mucoid strains of Pseudomonas aeruginosa: comparison of susceptibility to opsonic antibody in mucoid and nonmucoid strains | Q41574037 | ||
| Effect of changing airway mechanics on maximum expiratory flow | Q41903133 | ||
| The lung in cystic fibrosis. A quantitative study including prevalence of pathologic findings among different age groups | Q42038566 | ||
| Levels of free granulocyte elastase in bronchial secretions from patients with cystic fibrosis: effect of antimicrobial treatment against Pseudomonas aeruginosa | Q44412123 | ||
| Obstructive disease of the airways in cystic fibrosis | Q45244117 | ||
| Pseudomonas hyperimmune globulin passive immunotherapy for pulmonary exacerbations in cystic fibrosis | Q46063609 | ||
| Pulmonary mucociliary clearance in cystic fibrosis | Q48013742 | ||
| Role of conventional physiotherapy in cystic fibrosis. | Q50563978 | ||
| Regional distribution of macroscopic lung disease in cystic fibrosis. | Q52643129 | ||
| Lung function abnormalities in cystic fibrosis and changes during growth | Q52774061 | ||
| Alternate-day prednisone reduces morbidity and improves pulmonary function in cystic fibrosis. | Q52868603 | ||
| Airway obstruction and airway wall instability in cystic fibrosis: The isolated and combined effect of theophylline and sympathomimetics | Q54390607 | ||
| The spectrum of cystic fibrosis. A study of pulmonary mechanics in 46 patients. | Q54647466 | ||
| Fibronectin binds to Staphylococcus aureus | Q59074971 | ||
| Proteolysis of human IgG by human polymorphonuclear leucocyte elastase produces an Fc fragment with in vitro biological activity | Q66940671 | ||
| Immunoglobulins and albumin in sputum from patients with cystic fibrosis. A study of protein stability and presence of proteases | Q67272968 | ||
| Reduction of sputum Pseudomonas aeruginosa density by antibiotics improves lung function in cystic fibrosis more than do bronchodilators and chest physiotherapy alone | Q67285211 | ||
| Randomized trial of ceftazidime versus placebo in the management of acute respiratory exacerbations in patients with cystic fibrosis | Q68205329 | ||
| Effect of airway instability and alveolar gas compression on bronchodilator-induced changes in flow-volume curves and airway resistance | Q68354241 | ||
| Acute and long-term amiloride inhalation in cystic fibrosis lung disease. A rational approach to cystic fibrosis therapy | Q68721870 | ||
| Forced expirations against a variable resistance: a new chest physiotherapy method in cystic fibrosis | Q68930735 | ||
| Lysosomal enzymes from polymorphonuclear leukocytes and proteinase inhibitors in patients with cystic fibrosis | Q68967630 | ||
| Quantitative aspects of lung pathology in cystic fibrosis | Q69584410 | ||
| Biochemical and pathologic evidence for proteolytic destruction of lung connective tissue in cystic fibrosis | Q69907533 | ||
| Heart-lung transplantation for cystic fibrosis | Q69921448 | ||
| Effects of long-term nutritional rehabilitation on body composition and clinical status in malnourished children and adolescents with cystic fibrosis | Q69955664 | ||
| Bronchodilators increase airway instability in cystic fibrosis | Q70102881 | ||
| Short-term pulmonary effects of total parenteral nutrition in children with cystic fibrosis | Q70476049 | ||
| Granulocyte neutral proteases and Pseudomonas elastase as possible causes of airway damage in patients with cystic fibrosis | Q70480655 | ||
| Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis | Q70982010 | ||
| Improved growth and clinical, nutritional, and respiratory changes in response to nutritional therapy in cystic fibrosis | Q71515779 | ||
| Pulmonary mechanics in asthma and cystic fibrosis | Q71800152 | ||
| Observations in cystic fibrosis of the pancreas. 3. Pulmonary lesions | Q72023657 | ||
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cystic fibrosis | Q178194 |
| P304 | page(s) | 10-17 | |
| P577 | publication date | 1991-01-01 | |
| P1433 | published in | Journal of the Royal Society of Medicine | Q6296198 |
| P1476 | title | Pathogenesis and management of lung disease in cystic fibrosis | |
| P478 | volume | 84 Suppl 18 |
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