Lung function in infants with cystic fibrosis.

Lung function was measured in 28 infants with cystic fibrosis and repeated in 17 of the infants during the first year of life. Thoracic gas volume (TGV) and specific airway conductance (sGaw) were measured plethysmographically and maximum forced expiratory flow at functional residual capacity (VmaxF...

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Bibliografiske detaljer
Main Authors: Beardsmore, C S, Bar-Yishay, E, Maayan, C, Yahav, Y, Katznelson, D, Godfrey, S
Format: Artigo
Sprog:Inglês
Udgivet: 1988
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC461366/
https://ncbi.nlm.nih.gov/pubmed/3212751
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