1. Adelaide Research & Scholarship

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Results 21-30 of 32 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1997The spectrum of primary immundeficiency disorders in AustraliaBaumgart, K.; Britton, W.; Kemp, A.; French, M.; Roberton, D.
2000Analysis of the breath hydrogen test for carbohydrate malabsorption: Validation of a pocket-sized breath test analysierLee, W.; Davidson, G.; Moore, D.; Butler, R.
1995Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic-sufficient patients with cystic fibrosisCouper, R.; Corey, M.; Durie, P.; Forstner, G.; Moore, D.
2005Enzyme replacement therapy for Gaucher disease in AustraliaGoldblatt, J.; Szer, J.; Fletcher, J.; McGill, J.; Rowell, J.; Wilson, M.
2001Nationwide study of haemolytic uraemic syndrome: clinical, microbiological, and epidemiological featuresElliott, E.; Robins-Browne, R.; O'Loughlin, E.; Bennett-Wood, V.; Bourke, J.; Henning, P.; Hogg, G.; Knight, J.; Powell, H.; Redmond, D.
2010Increased thrombophilic tendency in pediatric cystic fibrosis patientsWilliams, V.; Griffiths, A.; Yap, Z.; Martin, J.; Smith, G.; Couper, R.; Revesz, T.
2009Collagen type III alpha 1 is a gastro-oesophageal reflux disease susceptibility gene and a male risk factor for hiatus herniaAsling, B.; Jirholt, J.; Hammond, P.; Knutsson, M.; Walentinsson, A.; Davidson, G.; Agreus, L.; Lehmann, A.; Lagerstrom-Fermer, M.
2009A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technologyTalseth-Palmer, B.; Bowden, N.; Meldrum, C.; Nicholl, J.; Thompson, E.; Friend, K.; Liebelt, J.; Bratkovic, D.; Haan, E.; Yu, S.; Scott, R.
2009A Novel Bocavirus Associated with Acute Gastroenteritis in Australian ChildrenArthur, J.; Higgins, G.; Davidson, G.; Givney, R.; Ratcliff, R.; Münger, K.
2019Causes and characteristics of injury in paediatric major trauma and trends over timeBeck, B.; Teague, W.; Cameron, P.; Gabbe, B.J.

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