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Archives of Disease in Childhood|October 1, 1983
In vitro assessment of combined antibiotic and mucolytic treatment for Pseudomonas aeruginosa infection in cystic fibrosisD P Heaf, G J Webb, D J Matthew
Pediatric Pulmonology|March 1, 1987
Comparison of the occlusion and inflation techniques for measuring total respiratory compliance in sick, intubated infantsD P Heaf, H Turner, J Stocks, et al.
Archives of Disease in Childhood|December 1, 1990
Cystic fibrosis, Pseudomonas aeruginosa, and selective decontaminationA M Dalzell, H K van Saene, D P Heaf
The New England Journal of Medicine|June 23, 1983
Postural effects on gas exchange in infantsD P Heaf, P Helms, I Gordon, et al.
The Journal of Pediatrics|May 1, 1982
Nasopharyngeal airways in Pierre Robin SyndromeD P Heaf, P J Helms, R Dinwiddie, et al.
Archives of Disease in Childhood|June 1, 1990
Small intestinal permeability and orocaecal transit time in cystic fibrosisA M Dalzell, N S Freestone, D Billington, et al.
Thorax|April 1, 1991
Ceftazidime treatment in cystic fibrosis: resistant organisms in sputum and faecesA M Dalzell, D Sunderland, C A Hart, et al.
Pediatric Pulmonology|August 12, 2003
Methicillin-resistant Staphylococcus aureus in children with cystic fibrosis: An eradication protocolA Solís, D Brown, J Hughes, et al.
The Journal of Pediatrics|July 1, 1982
Changes in pulmonary function during the diuretic phase of respiratory distress syndromeD P Heaf, J Belik, A R Spitzer, et al.
Pediatric Pulmonology|July 1, 1992
Branhamella catarrhalis colonization in preschool asthmaticsP C Seddon, D Sunderland, S M O'Halloran, et al.
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