Head and neck manifestations of cystic fibrosis and ciliary dyskinesia

Otolaryngologic Clinics of North America

Volumn 33, Issue 6, 2000, Pages 1333-1341

  Hulka, Gregory F ^b  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

AMINOGLYCOSIDE ANTIBIOTIC AGENT; ANTIBIOTIC AGENT; ANTIHISTAMINIC AGENT; DEOXYRIBONUCLEASE; QUINOLINE DERIVED ANTIINFECTIVE AGENT; STEROID; URIDINE TRIPHOSPHATE;

ANTIBIOTIC THERAPY; CILIARY DYSKINESIA; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CYSTIC FIBROSIS; DISEASE ASSOCIATION; EAR DISEASE; HEAD AND NECK DISEASE; HUMAN; LAVAGE; OTITIS MEDIA; PATHOGENESIS; PATHOPHYSIOLOGY; REVIEW; SINUSITIS; STEROID THERAPY;

EID: 0034531180     PISSN: 00306665     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0030-6665(05)70284-X     Document Type: Article

References (27)

1. Asymmetry of cilia and of mice and men
2. Intraoperative diagnosis of primary ciliary dyskinesia
3. Pathological changes of the lateral nasal wall in patients with cystic fibrosis (mucoviddosis)
4. Two rights make a wrong: Human left-right malformations
5. Incidence of primary ciliary dyskinesia in children with recurrent respiratory diseases
6. Management of chronic sinusitis m cystic fibrosis
7. Paranasal sinus mucoceles in cystic fibrosis
8. Results of tympanoplasty in children with primary ciliary dyskinesia
9. Longitudinal study of lung function in a cohort of primary source
10. Otological manifestations of primary ciliary dyskinesia
11. Treatment of otitis media with effusion in children with primary ciliary dyskinesia
12. Regulation of mucociliary clearance in health and disease
13. A possible mechanism of primary ciliary dyskinesia: A case of a segmental defect in ciliary microtubules
14. Correlations among mucociliary transport, ciliary function, and ciliary structure
15. Nasal and lower airway level of nitric oxide in children
16. Identification of the cystic fibrosis gene: Genetic analysis
17. The evaluation of ciliary function: Electron versus light microscopy
18. Management of sinusitis in cystic fibrosis by endoscopic surgery and serial antimicrobial lavage
19. Cystic fibrosis in adults: Diagnosis and management
20. Effect of aerosolized uridine-5′-triphosphate on airway: Clearance with cough in patients with primary ciliary dyskinesia
21. Sinusitis and cystic fibrosis
22. Chloride impermeability in cystic fibrosis
23. Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
24. Identification of the cystic fibrosis gene: Chromosome walking and jumping
25. Polypoidal rhinosinusitis in cystic fibrosis: A clinical and histopathological study
26. Ciliary motility at light microscopy: A screening technique for ciliary defects
27. Lung transplantation in cystic fibrosis