Gender differences in cystic fibrosis: Pseudomonas aeruginosa infection

Journal of Clinical Epidemiology

Volumn 48, Issue 8, 1995, Pages 1041-1049

  Demko, Catherine A ^a,b   Byard, Pamela J ^a,b   Davis, Pamela B ^a,b  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

^b CASE WESTERN RESERVE UNIVERSITY   (United States)

Author keywords

Cystic fibrosis; Gender differences; Pseudomonas aeruginosa

Indexed keywords

ARTICLE; CHILD; CYSTIC FIBROSIS; FEMALE; FORCED EXPIRATORY VOLUME; GRAM NEGATIVE INFECTION; HUMAN; LUNG DISEASE; LUNG FUNCTION TEST; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PSEUDOMONAS AERUGINOSA; SCORING SYSTEM; SEX DIFFERENCE; SURVIVAL TIME; THORAX RADIOGRAPHY;

ADOLESCENT; AGE FACTORS; CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; FEMALE; HUMAN; INFANT; LIKELIHOOD FUNCTIONS; MALE; PROGNOSIS; PSEUDOMONAS AERUGINOSA; PSEUDOMONAS INFECTIONS; REGRESSION ANALYSIS; RESPIRATORY FUNCTION TESTS; RESPIRATORY TRACT INFECTIONS; SEX FACTORS; SUPPORT, U.S. GOV'T, P.H.S.; SURVIVAL ANALYSIS;

EID: 0029016495     PISSN: 08954356     EISSN: None     Source Type: Journal    
DOI: 10.1016/0895-4356(94)00230-N     Document Type: Article

References (32)

1. The changing epidemiology of cystic fibrosis
2. Relationship between clinical parameters and linear growth in children with cystic fibrosis
3. The adolescent growth spurt in children with cystic fibrosis
4. Pulmonary disease associated with Pseudomonas aeruginosa in cystic fibrosis: Current status of the host-bacterium interaction
5. An atypical Pseudomonas aeruginosa associated with cystic fibrosis of the pancreas
6. Pseudomonas aeruginosa infection in cystic fibrosis
7. Microbiology of lung infection in cystic fibrosis patients
8. Mucoid Pseudomonas aeruginosa is a marker of poor survival in cystic fibrosis
9. Multiple isolates of Pseudomonas aeruginosa with differing antimicrobial susceptibility patterns from patients with cystic fibrosis
10. Mucoid Pseudomonas aeruginosa in cystic fibrosis
11. Role of alginate in infection with mucoid Pseudomonas aeruginosa in cystic fibrosis
12. Pseudomonas and related genera
13. Cultures of thoracotomy specimens confirm usefulness of sputum cultures in cystic fibrosis
14. Predictive value of oropharyngeal cultures for identifying lower airway bacteria in cystic fibrosis patients
15. Comparison of throat with bronchoalveolar lavage cultures in determining lower airway bacterial colonization in cystic fibrosis
16. The identification of atypical strains of Pseudomonas aeruginosa
17. Long-term study of one hundred five patients with cystic fibrosis
18. Evaluation of a prophylactic and therapeutic program for patients with cystic fibrosis
19. Standardization of spirometry—1987 update
20. patients with cystic fibrosis with or without meconium ileus
21. Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization with Pseudomonas aeruginosa
22. Pseudomonas aeruginosa infection in cystic fibrosis, Relationship between mucoid strains of Pseudomonas aeruginosa and the humoral immune response
23. Characterization and use of a DNA probe as an epidemiological marker for Pseudomonas aeruginosa
24. In vivo regulation of virulence in Pseudomonas aeruginosa associated genetic rearrangement
25. Pulmonary dehydration and infection in cystic fibrosis: evidence that ethanol activates alginate gene expression and induction of mucoidy
26. High osmolarity is a signal for enhanced aged transcription in mucoid and nonmucoid Pseudomonas aeruginosa strains
27. Role of energy metabolism in conversion of nonmucoid Pseudomonas aeruginosa to the mucoid phenotype
28. Heterogeneity, persistence, and distribution of Pseudomonas aeruginosa genotypes in cystic fibrosis patients
29. Ecology of Pseudomonas aeruginosa in patients with cystic fibrosis
30. Molecular epidemiology of chronic pulmonary colonization by Pseudomonas aeruginosa in cystic fibrosis