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dc.contributor.authorGangell, C.
dc.contributor.authorHall, Graham
dc.contributor.authorBalding, E.
dc.contributor.authorBerry, L.
dc.contributor.authorCarlin, J.
dc.contributor.authorCarzino, R.
dc.contributor.authorde Klerk, N.
dc.contributor.authorDouglas, T.
dc.contributor.authorEbdon, A.
dc.contributor.authorFoo, C.
dc.contributor.authorGangell, C.
dc.contributor.authorGarratt, L.
dc.contributor.authorGibson, A.
dc.contributor.authorHarrison, J.
dc.contributor.authorKicic, A.
dc.contributor.authorLaing, I.
dc.contributor.authorLogie, K.
dc.contributor.authorMassie, J.
dc.contributor.authorMott, L.
dc.contributor.authorMurray, C.
dc.contributor.authorPoreddy, S.
dc.contributor.authorRanganathan, S.
dc.contributor.authorRobertson, C.
dc.contributor.authorRobins-Browne, R.
dc.contributor.authorRobinson, P.
dc.contributor.authorSkoric, B.
dc.date.accessioned2017-07-27T05:20:18Z
dc.date.available2017-07-27T05:20:18Z
dc.date.created2017-07-26T11:11:12Z
dc.date.issued2012
dc.identifier.citationGangell, C. and Hall, G. and Balding, E. and Berry, L. and Carlin, J. and Carzino, R. and de Klerk, N. et al. 2012. Early detection of lung function abnormalities in young children with cystic fibrosis. Annals of Respiratory Medicine. 2 (1): pp. 22-27.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/54273
dc.description.abstract

The onset of lung disease in cystic fibrosis (CF) begins early in life with respiratory infection, inflammation, and structural lung damage all reported in infants with CF in the first months of life. As new treatments become available, it is essential that we have outcome measures that can be used to track disease progression and treatment efficacy. In this review, we have examined the role of lung function testing in infants and preschool children with CF. In particular, we have focused on the ability of the various lung function tests to detect the presence of respiratory pathogens and structural lung disease, increased inflammation, and the onset of acute exacerbations.

dc.titleEarly detection of lung function abnormalities in young children with cystic fibrosis
dc.typeJournal Article
dcterms.source.volume2
dcterms.source.number1
dcterms.source.startPage22
dcterms.source.endPage27
dcterms.source.issn2042-4701
dcterms.source.titleAnnals of Respiratory Medicine
curtin.departmentSchool of Physiotherapy and Exercise Science
curtin.accessStatusFulltext not available


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