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dc.contributor.authorJudge, Eoin P
dc.contributor.authorDodd, Jonathan D
dc.contributor.authorMasterson, James B
dc.contributor.authorGallagher, Charles G
dc.date.accessioned2012-11-28T12:29:47Z
dc.date.available2012-11-28T12:29:47Z
dc.date.issued2006-11
dc.identifier.citationPulmonary abnormalities on high-resolution CT demonstrate more rapid decline than FEV1 in adults with cystic fibrosis. 2006, 130 (5):1424-32 Chesten_GB
dc.identifier.issn0012-3692
dc.identifier.pmid17099020
dc.identifier.doi10.1378/chest.130.5.1424
dc.identifier.urihttp://hdl.handle.net/10147/253661
dc.description.abstractFEV1 may remain stable while high-resolution CT (HRCT) appearances deteriorate in children with cystic fibrosis (CF). However, spirometry results commonly decline in older age groups.
dc.language.isoenen
dc.rightsArchived with thanks to Chesten_GB
dc.subject.meshAdolescent
dc.subject.meshAdult
dc.subject.meshAnalysis of Variance
dc.subject.meshBronchiectasis
dc.subject.meshCystic Fibrosis
dc.subject.meshFemale
dc.subject.meshForced Expiratory Volume
dc.subject.meshHumans
dc.subject.meshLongitudinal Studies
dc.subject.meshLung
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshMucus
dc.subject.meshPseudomonas aeruginosa
dc.subject.meshSpirometry
dc.subject.meshSputum
dc.subject.meshTomography, X-Ray Computed
dc.titlePulmonary abnormalities on high-resolution CT demonstrate more rapid decline than FEV1 in adults with cystic fibrosis.en_GB
dc.typeArticleen
dc.contributor.departmentDepartment of Respiratory Medicine, St Vincent's University Hospital, Dublin, Ireland.en_GB
dc.identifier.journalChesten_GB
dc.description.provinceLeinsteren
html.description.abstractFEV1 may remain stable while high-resolution CT (HRCT) appearances deteriorate in children with cystic fibrosis (CF). However, spirometry results commonly decline in older age groups.


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