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PUBMED FOR HANDHELDS

Journal Abstract Search


115 related items for PubMed ID: 9620905

  • 41.
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  • 42. Cystic fibrosis and other respiratory diseases of impaired mucus clearance.
    Livraghi A, Randell SH.
    Toxicol Pathol; 2007 Jan; 35(1):116-29. PubMed ID: 17325980
    [Abstract] [Full Text] [Related]

  • 43. Role of magnesium in the failure of rhDNase therapy in patients with cystic fibrosis.
    Sanders NN, Franckx H, De Boeck K, Haustraete J, De Smedt SC, Demeester J.
    Thorax; 2006 Nov; 61(11):962-8. PubMed ID: 17071834
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  • 44. DNA quantification and fragmentation in sputum after inhalation of recombinant human deoxyribonuclease.
    Riethmueller J, Vonthein R, Borth-Bruhns T, Grassmé H, Eyrich M, Schilbach K, Stern M, Gulbins E.
    Cell Physiol Biochem; 2008 Nov; 22(1-4):347-52. PubMed ID: 18769062
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  • 45. Respiratory mucus from asymptomatic smokers is better hydrated and more easily cleared by mucociliary action.
    Rubin BK, Ramirez O, Zayas JG, Finegan B, King M.
    Am Rev Respir Dis; 1992 Mar; 145(3):545-7. PubMed ID: 1546833
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  • 46. Mucoactive agents for airway mucus hypersecretory diseases.
    Rogers DF.
    Respir Care; 2007 Sep; 52(9):1176-93; discussion 1193-7. PubMed ID: 17716385
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  • 47. Recombinant human DNase nebulisation in children with cystic fibrosis: before bedtime or after waking up?
    van der Giessen LJ, Gosselink R, Hop WC, Tiddens HA.
    Eur Respir J; 2007 Oct; 30(4):763-8. PubMed ID: 17596273
    [Abstract] [Full Text] [Related]

  • 48. Numerical and experimental investigation of mucociliary clearance breakdown in cystic fibrosis.
    Chatelin R, Anne-Archard D, Murris-Espin M, Thiriet M, Poncet P.
    J Biomech; 2017 Feb 28; 53():56-63. PubMed ID: 28117099
    [Abstract] [Full Text] [Related]

  • 49. Aerosolized recombinant human DNase in hospitalized cystic fibrosis patients with acute pulmonary exacerbations.
    Wilmott RW, Amin RS, Colin AA, DeVault A, Dozor AJ, Eigen H, Johnson C, Lester LA, McCoy K, McKean LP, Moss R, Nash ML, Jue CP, Regelmann W, Stokes DC, Fuchs HJ.
    Am J Respir Crit Care Med; 1996 Jun 28; 153(6 Pt 1):1914-7. PubMed ID: 8665055
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  • 54. Sodium chloride increases the ciliary transportability of cystic fibrosis and bronchiectasis sputum on the mucus-depleted bovine trachea.
    Wills PJ, Hall RL, Chan W, Cole PJ.
    J Clin Invest; 1997 Jan 01; 99(1):9-13. PubMed ID: 9011581
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  • 57. Inhaled dry powder mannitol in cystic fibrosis: an efficacy and safety study.
    Bilton D, Robinson P, Cooper P, Gallagher CG, Kolbe J, Fox H, Jaques A, Charlton B, CF301 Study Investigators.
    Eur Respir J; 2011 Nov 01; 38(5):1071-80. PubMed ID: 21478216
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  • 58.
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  • 59. Deficient hydrophilic lung surfactant proteins A and D with normal surfactant phospholipid molecular species in cystic fibrosis.
    Postle AD, Mander A, Reid KB, Wang JY, Wright SM, Moustaki M, Warner JO.
    Am J Respir Cell Mol Biol; 1999 Jan 01; 20(1):90-8. PubMed ID: 9870921
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  • 60.
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