C. E. Wainwright

Publication List Details

Period

2002 - 2008

Number

33

Co-Authors

Novel neutrophil-derived proteins in bronchoalveolar lavage fluid indicate an exaggerated inflammatory response in pediatric cystic fibrosis patients (2007)

McMorran, B. J., Patat, S. A. O., Carlin, J. B., Grimwood, K., Jones, A., Armstrong, D. S., ...

Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutrophilmediated tissue destruction, but its genesis and mechanisms remain poorly understood. To further...

The Nutritional Status of Children with Cystic Fibrosis (2006)

Murphy, A. J., Buntain, H. M., Wainwright, C. E., Davies, P. S. W.

The importance of nutritional intervention for children with cystic fibrosis (CF) is well recognised. It would be expected that the increase in knowledge over the past decade would be reflected in...

Population pharmacokinetics of itraconazole and its active metabolite hydroxy-itraconazole in paediatric cystic fibrosis and bone marrow transplant patients (2006)

Hennig, S., Wainwright, C. E., Bell, S. C., Miller, H., Friberg, L. E., Charles, B. G.

Objective: The objective of the study was to characterise the population pharmacokinetic properties of itraconazole and its active metabolite hydroxyitraconazole in a representative paediatric...

Clonal strains of Pseudomonas aeruginosa in paediatric and adult cystic fibrosis units (2004)

O'Carroll, M. R., Syrmis, M. W., Wainwright, C. E., Greer, R. M., Mitchell, P., Coulter, C., ...

Despite recent reports of clonal strains of Pseudomonas aeruginosa in cystic fibrosis (CF) units, the need for routine microbiological surveillance remains contentious. Sputum was collected...

The use of air displacement plethysmography in children and adolescents with cystic fibrosis (2004)

Murphy, A. J., Buntain, H. M., Wong, J. C. H., Greer, R. M., Wainwright, C. E., Davies, P. S. W

Objectives: The purpose of this paper was to evaluate the use of air displacement plethysmography ( ADP) in children and adolescents with cystic fibrosis (CF). Specifically, the primary aim of this...

Clonal strains of Pseudomonas aeruginosa in paediatric and adult cystic fibrosis units (2004)

O'Carroll, M. R., Syrmis, M. W., Wainwright, C. E., Greer, R. M., Mitchell, P., Coulter, C., ...

Despite recent reports of clonal strains of Pseudomonas aeruginosa in cystic fibrosis (CF) units, the need for routine microbiological surveillance remains contentious. Sputum was collected...

Bone mineral density in Australian children, adolescents and adults with cystic fibrosis: a controlled cross sectional study (2004)

Buntain, H. M., Greer, R., Schluter, P. J., Wong, J. C. H., Batch, J. A., Potter, J. M., ...

Background: Low bone mineral density (BMD) is recognised in individuals with cystic fibrosis (CF) although the pathogenesis remains unclear. The aims of this study were to compare BMD over a broad...

The use of air displacement plethysmography in children and adolescents with cystic fibrosis (2004)

Murphy, A. J., Buntain, H. M., Wong, J. C. H., Greer, R. M., Wainwright, C. E., Davies, P. S. W.

Objectives: The purpose of this paper was to evaluate the use of air displacement plethysmography (ADP) in children and adolescents with cystic fibrosis (CF). Specifically, the primary aim of this...

Abnormalities of the PTH-vitamin D axis and bone turnover markers in children, adolescents and adults with cystic fibrosis: comparison with healthy controls (2003)

Greer, R. M., Buntain, H. M., Wainwright, C. E., Potter, J. M., Wong, J. C., O'Rourke, P. K., ...

Abnormalities of calcium and vitamin D metabolism in cystic fibrosis (CF) are well documented. We tested the hypothesis that alterations in calcium metabolism are related to vitamin D deficiency, and...