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Journal Abstract Search

152 related items for PubMed ID: 7458059

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  • 25. Evidence of diminished FEV1 and FVC in 6-year-olds followed in the European Cystic Fibrosis Patient Registry, 2007-2009.
    VanDevanter DR, Pasta DJ.
    J Cyst Fibros; 2013 Dec; 12(6):786-9. PubMed ID: 23632449
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  • 26. Regression equations for spirometry in children aged 6 to 17 years in Delhi region.
    Chhabra SK, Vijayan VK, Rahman M, Mittal V, Singh PD.
    Indian J Chest Dis Allied Sci; 2012 Dec; 54(1):59-63. PubMed ID: 22779126
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  • 27. Lung function in patients with primary ciliary dyskinesia: an iPCD Cohort study.
    Halbeisen FS, Goutaki M, Spycher BD, Amirav I, Behan L, Boon M, Hogg C, Casaulta C, Crowley S, Haarman EG, Karadag B, Koerner-Rettberg C, Loebinger MR, Mazurek H, Morgan L, Nielsen KG, Omran H, Santamaria F, Schwerk N, Thouvenin G, Yiallouros P, Lucas JS, Latzin P, Kuehni CE.
    Eur Respir J; 2018 Aug; 52(2):. PubMed ID: 30049738
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  • 29. Changes in lung function measured by spirometry and the forced oscillation technique in cystic fibrosis patients undergoing treatment for respiratory tract exacerbation.
    Ren CL, Brucker JL, Rovitelli AK, Bordeaux KA.
    Pediatr Pulmonol; 2006 Apr; 41(4):345-9. PubMed ID: 16496336
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  • 30. Five- to seven-year course of pulmonary function in cystic fibrosis.
    Corey M, Levison H, Crozier D.
    Am Rev Respir Dis; 1976 Dec; 114(6):1085-92. PubMed ID: 1008344
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  • 33. Spirometric standards for healthy Nigerian children and adolescents.
    Olanrewaju DM.
    East Afr Med J; 1991 Oct; 68(10):812-9. PubMed ID: 1813304
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  • 34. Normal variations in spirometry in health following placebo inhalation.
    Jindal SK, Ramasubramanian V, Behera D.
    Indian J Med Res; 1994 Aug; 100():77-80. PubMed ID: 7927561
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  • 35. [Characterization of the physical capacity in children of the Chilean National Program of Cystic Fibrosis].
    Puppo H, Von Oetinger A, Benz E, Torres-Castro R, Zagolín M, Boza ML, Astorga L, Bozzo R, Jorquera P, Kogan R, Perillán J.
    Rev Chil Pediatr; 2018 Oct; 89(5):638-643. PubMed ID: 30571807
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  • 38. Lung clearance index predicts pulmonary exacerbations in young patients with cystic fibrosis.
    Vermeulen F, Proesmans M, Boon M, Havermans T, De Boeck K.
    Thorax; 2014 Jan; 69(1):39-45. PubMed ID: 24021874
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  • 39. Influence of thoracic spine postural disorders on cardiorespiratory parameters in children and adolescents with cystic fibrosis.
    Okuro RT, Côrrea EP, Conti PB, Ribeiro JD, Ribeiro MA, Schivinski CI.
    J Pediatr (Rio J); 2012 Jul; 88(4):310-6. PubMed ID: 22914878
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