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Journal Abstract Search

302 related items for PubMed ID: 24176992

  • 21.
    ; . PubMed ID:
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  • 22. Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis.
    Kozlowska WJ, Bush A, Wade A, Aurora P, Carr SB, Castle RA, Hoo AF, Lum S, Price J, Ranganathan S, Saunders C, Stanojevic S, Stroobant J, Wallis C, Stocks J, London Cystic Fibrosis Collaboration.
    Am J Respir Crit Care Med; 2008 Jul 01; 178(1):42-9. PubMed ID: 18403721
    [Abstract] [Full Text] [Related]

  • 23. The effect of early Pseudomonas aeruginosa treatment on lung function in pediatric cystic fibrosis.
    Amin R, Lam M, Dupuis A, Ratjen F.
    Pediatr Pulmonol; 2011 Jun 01; 46(6):554-8. PubMed ID: 21337727
    [Abstract] [Full Text] [Related]

  • 24. Lung function in South African children with cystic fibrosis.
    Zar HJ, Moore B, Argent A, Ireland J, Westwood AT.
    S Afr Med J; 1998 Aug 01; 88(8):994-7. PubMed ID: 9754213
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  • 25.
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  • 26. 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]

  • 27. Prospective evaluation of resting energy expenditure, nutritional status, pulmonary function, and genotype in children with cystic fibrosis.
    Zemel BS, Kawchak DA, Cnaan A, Zhao H, Scanlin TF, Stallings VA.
    Pediatr Res; 1996 Oct 01; 40(4):578-86. PubMed ID: 8888286
    [Abstract] [Full Text] [Related]

  • 28.
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  • 29. Predictors of deterioration of lung function in cystic fibrosis.
    Schaedel C, de Monestrol I, Hjelte L, Johannesson M, Kornfält R, Lindblad A, Strandvik B, Wahlgren L, Holmberg L.
    Pediatr Pulmonol; 2002 Jun 01; 33(6):483-91. PubMed ID: 12001283
    [Abstract] [Full Text] [Related]

  • 30.
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  • 31. Changes in lung function in young cystic fibrosis patients between two courses of intravenous antibiotics against Pseudomonas aeruginosa.
    Béghin L, Michaud L, Loeuille GA, Wizla-Derambure N, Sayah H, Sardet A, Thumerelle C, Deschildre A, Turck D, Gottrand F.
    Pediatr Pulmonol; 2009 May 01; 44(5):464-71. PubMed ID: 19360849
    [Abstract] [Full Text] [Related]

  • 32. Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization with Pseudomonas aeruginosa.
    Kerem E, Corey M, Gold R, Levison H.
    J Pediatr; 1990 May 01; 116(5):714-9. PubMed ID: 2109790
    [Abstract] [Full Text] [Related]

  • 33. Assessment of Aspergillus sensitization or persistent carriage as a factor in lung function impairment in cystic fibrosis patients.
    Fillaux J, Brémont F, Murris M, Cassaing S, Rittié JL, Tétu L, Segonds C, Abbal M, Bieth E, Berry A, Pipy B, Magnaval JF.
    Scand J Infect Dis; 2012 Nov 01; 44(11):842-7. PubMed ID: 22831545
    [Abstract] [Full Text] [Related]

  • 34.
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  • 35. Longitudinal assessment of lung function from infancy to childhood in patients with cystic fibrosis.
    Harrison AN, Regelmann WE, Zirbes JM, Milla CE.
    Pediatr Pulmonol; 2009 Apr 01; 44(4):330-9. PubMed ID: 19274621
    [Abstract] [Full Text] [Related]

  • 36. Infections with Pseudomonas aeruginosa in patients with cystic fibrosis.
    Tümmler B, Bosshammer J, Breitenstein S, Brockhausen I, Gudowius P, Herrmann C, Herrmann S, Heuer T, Kubesch P, Mekus F, Römling U, Schmidt KD, Spangenberg C, Walter S.
    Behring Inst Mitt; 1997 Feb 01; (98):249-55. PubMed ID: 9382747
    [Abstract] [Full Text] [Related]

  • 37. Jointly modelling the relationship between survival and pulmonary function in cystic fibrosis patients.
    Schluchter MD, Konstan MW, Davis PB.
    Stat Med; 2002 May 15; 21(9):1271-87. PubMed ID: 12111878
    [Abstract] [Full Text] [Related]

  • 38.
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  • 39. Probability of treatment following acute decline in lung function in children with cystic fibrosis is related to baseline pulmonary function.
    Morgan WJ, Wagener JS, Yegin A, Pasta DJ, Millar SJ, Konstan MW, Scientific Advisory Group, investigators, coordinators of the Epidemiologic Study of Cystic Fibrosis.
    J Pediatr; 2013 Oct 15; 163(4):1152-7.e2. PubMed ID: 23810128
    [Abstract] [Full Text] [Related]

  • 40. 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]

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