Early detection of lung function abnormalities in young children with cystic fibrosis
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...
| Main Authors: | Gangell, C., Hall, Graham, Balding, E., Berry, L., Carlin, J., Carzino, R., de Klerk, N., Douglas, T., Ebdon, A., Foo, C., Garratt, L., Gibson, A., Harrison, J., Kicic, A., Laing, I., Logie, K., Massie, J., Mott, L., Murray, C., Poreddy, S., Ranganathan, S., Robertson, C., Robins-Browne, R., Robinson, P., Skoric, B. |
|---|---|
| Format: | Journal Article |
| Published: |
2012
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| Online Access: | http://hdl.handle.net/20.500.11937/54273 |
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