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3. Mucoactive agents for chronic, non-cystic fibrosis lung disease: A systematic review and meta-analysis. Tarrant BJ; Le Maitre C; Romero L; Steward R; Button BM; Thompson BR; Holland AE Respirology; 2017 Aug; 22(6):1084-1092. PubMed ID: 28397992 [TBL] [Abstract][Full Text] [Related]
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7. The immotile-cilia syndrome compared to other obstructive lung diseases: a clue to their pathogenesis. Mossberg B; Camner P; Afzelius BA Eur J Respir Dis Suppl; 1983; 127():129-36. PubMed ID: 6604645 [TBL] [Abstract][Full Text] [Related]
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9. Cystic fibrosis. An overview. Ruzal-Shapiro C Radiol Clin North Am; 1998 Jan; 36(1):143-61. PubMed ID: 9465872 [TBL] [Abstract][Full Text] [Related]
10. Nasal mucociliary clearance and ciliary beat frequency in cystic fibrosis compared with sinusitis and bronchiectasis. Rutland J; Cole PJ Thorax; 1981 Sep; 36(9):654-8. PubMed ID: 7314040 [TBL] [Abstract][Full Text] [Related]
11. Ciliary function in health and disease. Greenstone M; Cole PJ Br J Dis Chest; 1985 Jan; 79(1):9-26. PubMed ID: 3885993 [No Abstract] [Full Text] [Related]
12. [Mucociliary transport in obstructive lung disease]. Lieberman D; Kieberman D Harefuah; 1987 Apr; 112(7):338-41. PubMed ID: 3305238 [No Abstract] [Full Text] [Related]
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14. Management of airway mucus hypersecretion in chronic airway inflammatory disease: Chinese expert consensus (English edition). Shen Y; Huang S; Kang J; Lin J; Lai K; Sun Y; Xiao W; Yang L; Yao W; Cai S; Huang K; Wen F Int J Chron Obstruct Pulmon Dis; 2018; 13():399-407. PubMed ID: 29430174 [TBL] [Abstract][Full Text] [Related]
15. Mucociliary transport and cough as clearance mechanisms in obstructive lung disease. Mossberg B; Camner P Eur J Respir Dis Suppl; 1980; 111():18-20. PubMed ID: 6938404 [No Abstract] [Full Text] [Related]
16. Evaluation of nebulised hypertonic saline (7%) as an adjunct to physiotherapy in patients with stable bronchiectasis. Kellett F; Redfern J; Niven RM Respir Med; 2005 Jan; 99(1):27-31. PubMed ID: 15672845 [TBL] [Abstract][Full Text] [Related]
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19. Physical and functional properties of airway secretions in cystic fibrosis--therapeutic approaches. Puchelle E; de Bentzmann S; Zahm JM Respiration; 1995; 62 Suppl 1():2-12. PubMed ID: 7792436 [TBL] [Abstract][Full Text] [Related]
20. Rheology of cystic fibrosis sputum after in vitro treatment with hypertonic saline alone and in combination with recombinant human deoxyribonuclease I. King M; Dasgupta B; Tomkiewicz RP; Brown NE Am J Respir Crit Care Med; 1997 Jul; 156(1):173-7. PubMed ID: 9230743 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]