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Journal Abstract Search

164 related items for PubMed ID: 22081559

  • 21. Three-center feasibility of lung clearance index in infants and preschool children with cystic fibrosis and other lung diseases.
    Stahl M, Graeber SY, Joachim C, Barth S, Ricklefs I, Diekmann G, Kopp MV, Naehrlich L, Mall MA.
    J Cyst Fibros; 2018 Mar; 17(2):249-255. PubMed ID: 28811149
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  • 22. Multiple breath washout is feasible in the clinical setting and detects abnormal lung function in infants and young children with cystic fibrosis.
    Stahl M, Joachim C, Blessing K, Hämmerling S, Sommerburg O, Latzin P, Mall MA.
    Respiration; 2014 Mar; 87(5):357-63. PubMed ID: 24434651
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  • 23. Evaluation and use of childhood lung function tests in cystic fibrosis.
    Stocks J, Thia LP, Sonnappa S.
    Curr Opin Pulm Med; 2012 Nov; 18(6):602-8. PubMed ID: 23026833
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  • 24. Lung clearance index is a sensitive, repeatable and practical measure of airways disease in adults with cystic fibrosis.
    Horsley AR, Gustafsson PM, Macleod KA, Saunders C, Greening AP, Porteous DJ, Davies JC, Cunningham S, Alton EW, Innes JA.
    Thorax; 2008 Feb; 63(2):135-40. PubMed ID: 17675315
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  • 25. Bronchodilator responsiveness using spirometry in healthy and asthmatic preschool children.
    Borrego LM, Stocks J, Almeida I, Stanojevic S, Antunes J, Leiria-Pinto P, Rosado-Pinto JE, Hoo AF.
    Arch Dis Child; 2013 Feb; 98(2):112-7. PubMed ID: 23292523
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  • 26. 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
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  • 27. Progression of Lung Disease in Preschool Patients with Cystic Fibrosis.
    Stanojevic S, Davis SD, Retsch-Bogart G, Webster H, Davis M, Johnson RC, Jensen R, Pizarro ME, Kane M, Clem CC, Schornick L, Subbarao P, Ratjen FA.
    Am J Respir Crit Care Med; 2017 May 01; 195(9):1216-1225. PubMed ID: 27943680
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  • 31. Prevalence and impact on FEV(1) decline of chronic methicillin-resistant Staphylococcus aureus (MRSA) colonization in patients with cystic fibrosis. A single-center, case control study of 165 patients.
    Vanderhelst E, De Meirleir L, Verbanck S, Piérard D, Vincken W, Malfroot A.
    J Cyst Fibros; 2012 Jan 01; 11(1):2-7. PubMed ID: 21907637
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  • 33. 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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  • 34. Quantitative evaluation of hyperpolarized helium-3 magnetic resonance imaging of lung function variability in cystic fibrosis.
    Kirby M, Svenningsen S, Ahmed H, Wheatley A, Etemad-Rezai R, Paterson NA, Parraga G.
    Acad Radiol; 2011 Aug 01; 18(8):1006-13. PubMed ID: 21536462
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  • 35. Practicability of nitrogen multiple-breath washout measurements in a pediatric cystic fibrosis outpatient setting.
    Singer F, Kieninger E, Abbas C, Yammine S, Fuchs O, Proietti E, Regamey N, Casaulta C, Frey U, Latzin P.
    Pediatr Pulmonol; 2013 Aug 01; 48(8):739-46. PubMed ID: 22888105
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