Serial lung function studies in cystic fibrosis in the first 5 years of life.

Author:

Godfrey S,Mearns M,Howlett G

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference7 articles.

1. A rapid plethysmographic method for measuring thoracic gas volume: a comparison with a nitrogen washout method for measuring functional residual capacity in normal subjects;DuBois, A.B.; Botelho, S.Y.; Bedell, G.N.; Marshall, R.; Comroe, Jr, J.H.;Journal of Clinical Investigation,1956

2. Lung mechanics in normal infants and infants with congenital heart disease;Howlett, G.;Archives of Disease in Childhood,1972

3. Early detection ofpulmonary function abnormalities in cystic fibrosis;Lamarre, A.; Reilly, B.J.; Bryan, A.C.; Levison, H.;Pediatrics,1972

4. Ventilatory function in infants with cystic fibrosis;Phelan, P.D.; Gracey, M.; Williams, H.E.; Anderson, C.M.;Archives of Disease in Childhood,1969

5. The clinical application of regional lung function studies in infants and small children using 13N;Ronchetti, R.; Stocks, J.; Freedman, N.; Glass, H.; Godfrey, S.;Archives of Disease in Childhood,1975

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