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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Bibliografske podrobnosti
Main Authors: Beardsmore, C S, Bar-Yishay, E, Maayan, C, Yahav, Y, Katznelson, D, Godfrey, S
Format: Artigo
Jezik:Inglês
Izdano: 1988
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC461366/
https://ncbi.nlm.nih.gov/pubmed/3212751
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