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Journal Abstract Search

161 related items for PubMed ID: 22081584

  • 1. Analysis of the associations between lung function and clinical features in preschool children with cystic fibrosis.
    Ren CL, Rosenfeld M, Mayer OH, Davis SD, Kloster M, Castile RG, Hiatt PW, Hart M, Johnson R, Jones P, Brumback LC, Kerby GS.
    Pediatr Pulmonol; 2012 Jun; 47(6):574-81. PubMed ID: 22081584
    [Abstract] [Full Text] [Related]

  • 2. Lung function distinguishes preschool children with CF from healthy controls in a multi-center setting.
    Kerby GS, Rosenfeld M, Ren CL, Mayer OH, Brumback L, Castile R, Hart MA, Hiatt P, Kloster M, Johnson R, Jones P, Davis SD.
    Pediatr Pulmonol; 2012 Jun; 47(6):597-605. PubMed ID: 22081559
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  • 3. 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
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  • 4. Baseline characteristics and factors associated with nutritional and pulmonary status at enrollment in the cystic fibrosis EPIC observational cohort.
    Rosenfeld M, Emerson J, McNamara S, Joubran K, Retsch-Bogart G, Graff GR, Gutierrez HH, Kanga JF, Lahiri T, Noyes B, Ramsey B, Ren CL, Schechter M, Morgan W, Gibson RL, EPIC Study Group Participating Clinical Sites.
    Pediatr Pulmonol; 2010 Sep 01; 45(9):934-44. PubMed ID: 20597081
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  • 5. 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
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  • 6. 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
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  • 7. Mucus removal is impaired in children with cystic fibrosis who have been infected by Pseudomonas aeruginosa.
    Laube BL, Sharpless G, Benson J, Carson KA, Mogayzel PJ.
    J Pediatr; 2014 Apr 01; 164(4):839-45. PubMed ID: 24373575
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  • 12. 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 01; 45(6):601-7. PubMed ID: 20503286
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  • 13. 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 01; 43(3):817-23. PubMed ID: 24176992
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  • 14. Spirometry in early childhood in cystic fibrosis patients.
    Vilozni D, Bentur L, Efrati O, Minuskin T, Barak A, Szeinberg A, Blau H, Picard E, Kerem E, Yahav Y, Augarten A.
    Chest; 2007 Feb 01; 131(2):356-61. PubMed ID: 17296633
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  • 15. Spirometry in 3- to 6-year-old children with cystic fibrosis.
    Marostica PJ, Weist AD, Eigen H, Angelicchio C, Christoph K, Savage J, Grant D, Tepper RS.
    Am J Respir Crit Care Med; 2002 Jul 01; 166(1):67-71. PubMed ID: 12091173
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  • 16. Pulmonary function tests in preschool children with cystic fibrosis.
    Beydon N, Amsallem F, Bellet M, Boulé M, Chaussain M, Denjean A, Matran R, Pin I, Alberti C, Gaultier C.
    Am J Respir Crit Care Med; 2002 Oct 15; 166(8):1099-104. PubMed ID: 12379554
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  • 17. Growth in prepubertal children with cystic fibrosis, homozygous for the Delta F508 mutation.
    Keller BM, Aebischer CC, Kraemer R, Schöni MH.
    J Cyst Fibros; 2003 Jun 15; 2(2):76-83. PubMed ID: 15463854
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  • 19. Chronic Pseudomonas aeruginosa infection and respiratory muscle impairment in cystic fibrosis.
    Dassios TG, Katelari A, Doudounakis S, Dimitriou G.
    Respir Care; 2014 Mar 15; 59(3):363-70. PubMed ID: 23983273
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