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Journal Abstract Search

297 related items for PubMed ID: 15531750

  • 1. Ventilation inhomogeneities in relation to standard lung function in patients with cystic fibrosis.
    Kraemer R, Blum A, Schibler A, Ammann RA, Gallati S.
    Am J Respir Crit Care Med; 2005 Feb 15; 171(4):371-8. PubMed ID: 15531750
    [Abstract] [Full Text] [Related]

  • 2. Progression of pulmonary hyperinflation and trapped gas associated with genetic and environmental factors in children with cystic fibrosis.
    Kraemer R, Baldwin DN, Ammann RA, Frey U, Gallati S.
    Respir Res; 2006 Nov 30; 7(1):138. PubMed ID: 17137500
    [Abstract] [Full Text] [Related]

  • 3. Effect of allergic bronchopulmonary aspergillosis on lung function in children with cystic fibrosis.
    Kraemer R, Deloséa N, Ballinari P, Gallati S, Crameri R.
    Am J Respir Crit Care Med; 2006 Dec 01; 174(11):1211-20. PubMed ID: 16959918
    [Abstract] [Full Text] [Related]

  • 4. Early cystic fibrosis lung disease detected by bronchoalveolar lavage and lung clearance index.
    Belessis Y, Dixon B, Hawkins G, Pereira J, Peat J, MacDonald R, Field P, Numa A, Morton J, Lui K, Jaffe A.
    Am J Respir Crit Care Med; 2012 Apr 15; 185(8):862-73. PubMed ID: 22323305
    [Abstract] [Full Text] [Related]

  • 5. Determining presence of lung disease in young children with cystic fibrosis: lung clearance index, oxygen saturation and cough frequency.
    Bakker EM, van der Meijden JC, Nieuwhof EM, Hop WC, Tiddens HA.
    J Cyst Fibros; 2012 May 15; 11(3):223-30. PubMed ID: 22265603
    [Abstract] [Full Text] [Related]

  • 6. Lung clearance index in the assessment of airways disease.
    Horsley A.
    Respir Med; 2009 Jun 15; 103(6):793-9. PubMed ID: 19246184
    [Abstract] [Full Text] [Related]

  • 7. Effects of cystic fibrosis lung disease on gas mixing indices derived from alveolar slope analysis.
    Horsley AR, Macleod KA, Robson AG, Lenney J, Bell NJ, Cunningham S, Greening AP, Gustafsson PM, Innes JA.
    Respir Physiol Neurobiol; 2008 Aug 31; 162(3):197-203. PubMed ID: 18625345
    [Abstract] [Full Text] [Related]

  • 8. Improvements in lung function outcomes in children with cystic fibrosis are associated with better nutrition, fewer chronic pseudomonas aeruginosa infections, and dornase alfa use.
    McPhail GL, Acton JD, Fenchel MC, Amin RS, Seid M.
    J Pediatr; 2008 Dec 31; 153(6):752-7. PubMed ID: 18760423
    [Abstract] [Full Text] [Related]

  • 9. Multiple-breath washout as a marker of lung disease in preschool children with cystic fibrosis.
    Aurora P, Bush A, Gustafsson P, Oliver C, Wallis C, Price J, Stroobant J, Carr S, Stocks J, London Cystic Fibrosis Collaboration.
    Am J Respir Crit Care Med; 2005 Feb 01; 171(3):249-56. PubMed ID: 15516530
    [Abstract] [Full Text] [Related]

  • 10. Using index of ventilation to assess response to treatment for acute pulmonary exacerbation in children with cystic fibrosis.
    Robinson PD, Cooper P, Van Asperen P, Fitzgerald D, Selvadurai H.
    Pediatr Pulmonol; 2009 Aug 01; 44(8):733-42. PubMed ID: 19598271
    [Abstract] [Full Text] [Related]

  • 11. Modulatory effect of the SLC9A3 gene on susceptibility to infections and pulmonary function in children with cystic fibrosis.
    Dorfman R, Taylor C, Lin F, Sun L, Sandford A, Paré P, Berthiaume Y, Corey M, Durie P, Zielenski J, Members of Canadian Consortium for CF Genetic Studies.
    Pediatr Pulmonol; 2011 Apr 01; 46(4):385-92. PubMed ID: 20967843
    [Abstract] [Full Text] [Related]

  • 12. Sensitivity of Lung Clearance Index and chest computed tomography in early CF lung disease.
    Ellemunter H, Fuchs SI, Unsinn KM, Freund MC, Waltner-Romen M, Steinkamp G, Gappa M.
    Respir Med; 2010 Dec 01; 104(12):1834-42. PubMed ID: 20637585
    [Abstract] [Full Text] [Related]

  • 13. Early detection of lung disease and its association with the nutritional status, genetic background and life events in patients with cystic fibrosis.
    Kraemer R, Aebi C, Casaulta Aebischer C, Gallati S.
    Respiration; 2000 Dec 01; 67(5):477-90. PubMed ID: 11070449
    [Abstract] [Full Text] [Related]

  • 14. Long-term gas exchange characteristics as markers of deterioration in patients with cystic fibrosis.
    Kraemer R, Latzin P, Pramana I, Ballinari P, Gallati S, Frey U.
    Respir Res; 2009 Nov 12; 10(1):106. PubMed ID: 19909502
    [Abstract] [Full Text] [Related]

  • 15. Longitudinal relationship between physical activity and lung health in patients with cystic fibrosis.
    Schneiderman JE, Wilkes DL, Atenafu EG, Nguyen T, Wells GD, Alarie N, Tullis E, Lands LC, Coates AL, Corey M, Ratjen F.
    Eur Respir J; 2014 Mar 12; 43(3):817-23. PubMed ID: 24176992
    [Abstract] [Full Text] [Related]

  • 16. Multiple breath inert gas washout as a measure of ventilation distribution in children with cystic fibrosis.
    Aurora P, Gustafsson P, Bush A, Lindblad A, Oliver C, Wallis CE, Stocks J.
    Thorax; 2004 Dec 12; 59(12):1068-73. PubMed ID: 15563707
    [Abstract] [Full Text] [Related]

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  • 19. Long-term effects of birth order and age at diagnosis in cystic fibrosis: a sibling cohort study.
    Slieker MG, van den Berg JM, Kouwenberg J, van Berkhout FT, Heijerman HG, van der Ent CK.
    Pediatr Pulmonol; 2010 Jun 12; 45(6):601-7. PubMed ID: 20503286
    [Abstract] [Full Text] [Related]

  • 20. Infection, inflammation, and lung function decline in infants with cystic fibrosis.
    Pillarisetti N, Williamson E, Linnane B, Skoric B, Robertson CF, Robinson P, Massie J, Hall GL, Sly P, Stick S, Ranganathan S, Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST CF).
    Am J Respir Crit Care Med; 2011 Jul 01; 184(1):75-81. PubMed ID: 21493738
    [Abstract] [Full Text] [Related]

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