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- W2030529323 abstract "Measurement of lung function is central to the monitoring of cystic fibrosis (CF) lung disease and is used routinely as soon as children are able to reliably reproduce forced respiratory manoeuvres. Falling or persistently poor lung function indices are of concern and trigger further investigations to discover the cause as well as escalations in treatment. We describe a previously unreported cause of persistently poor spirometry in CF and highlight important considerations in the differential diagnosis of children with reduced lung function." @default.
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- W2030529323 date "2010-06-23" @default.
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- W2030529323 title "Manifesting carriage of a Duchenne muscular dystrophy mutation: an unusual cause of impaired lung function in CF" @default.
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- W2030529323 doi "https://doi.org/10.1258/jrsm.2010.s11007" @default.
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