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Journal Abstract Search

431 related items for PubMed ID: 9674466

  • 1. Sputum rheology changes in cystic fibrosis lung disease following two different types of physiotherapy: flutter vs autogenic drainage.
    App EM, Kieselmann R, Reinhardt D, Lindemann H, Dasgupta B, King M, Brand P.
    Chest; 1998 Jul; 114(1):171-7. PubMed ID: 9674466
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  • 2. Improved clearability of cystic fibrosis sputum with dextran treatment in vitro.
    Feng W, Garrett H, Speert DP, King M.
    Am J Respir Crit Care Med; 1998 Mar; 157(3 Pt 1):710-4. PubMed ID: 9517580
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  • 4. Acute effects of combined exercise and oscillatory positive expiratory pressure therapy on sputum properties and lung diffusing capacity in cystic fibrosis: a randomized, controlled, crossover trial.
    Radtke T, Böni L, Bohnacker P, Maggi-Beba M, Fischer P, Kriemler S, Benden C, Dressel H.
    BMC Pulm Med; 2018 Jun 14; 18(1):99. PubMed ID: 29898704
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  • 5. The Short-Term Effect of Breathing Tasks Via an Incentive Spirometer on Lung Function Compared With Autogenic Drainage in Subjects With Cystic Fibrosis.
    Sokol G, Vilozni D, Hakimi R, Lavie M, Sarouk I, Bat-El Bar, Dagan A, Ofek M, Efrati O.
    Respir Care; 2015 Dec 14; 60(12):1819-25. PubMed ID: 26374905
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  • 6. The effect of a first-generation antihistamine on sputum viscoelasticity in cystic fibrosis.
    Homnick DN, Marks JH, Rubin BK.
    J Aerosol Med; 2007 Dec 14; 20(1):45-9. PubMed ID: 17388752
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  • 7. Cystic Fibrosis Sputum Rheology Correlates With Both Acute and Longitudinal Changes in Lung Function.
    Ma JT, Tang C, Kang L, Voynow JA, Rubin BK.
    Chest; 2018 Aug 14; 154(2):370-377. PubMed ID: 29559310
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  • 8. Effects of flutter and PEP mask physiotherapy on symptoms and lung function in children with cystic fibrosis.
    van Winden CM, Visser A, Hop W, Sterk PJ, Beckers S, de Jongste JC.
    Eur Respir J; 1998 Jul 14; 12(1):143-7. PubMed ID: 9701429
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  • 12. In vivo effects of recombinant human DNase I on sputum in patients with cystic fibrosis.
    Shah PL, Scott SF, Knight RA, Marriott C, Ranasinha C, Hodson ME.
    Thorax; 1996 Feb 14; 51(2):119-25. PubMed ID: 8711640
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  • 16. Inhaled mannitol improves the hydration and surface properties of sputum in patients with cystic fibrosis.
    Daviskas E, Anderson SD, Jaques A, Charlton B.
    Chest; 2010 Apr 14; 137(4):861-8. PubMed ID: 19880909
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  • 17. Revisited physicochemical and transport properties of respiratory mucus in genotyped cystic fibrosis patients.
    Deneuville E, Perrot-Minot C, Pennaforte F, Roussey M, Zahm JM, Clavel C, Puchelle E, de Bentzmann S.
    Am J Respir Crit Care Med; 1997 Jul 14; 156(1):166-72. PubMed ID: 9230742
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