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Results 21-30 of 35 (Search time: 0.002 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.
2008Familial 22q11.2 duplication: a three-generation family with a 3-Mb duplication and a familial 1.5-Mb duplicationYu, S.; Cox, K.; Friend, K.; Smith, S.; Buchheim, R.; Bain, S.; Leibelt, J.; Thompson, E.; Bratkovic, D.
2005Frequency of truly cryptic subtelomere abnormalities - a study of 534 patients and literature reviewYu, S.; Baker, E.; Hinton, L.; Eyre, H.; Waters, W.; Higgins, S.; Sutherland, G.; Haan, E.
2007Immunomodulatory constituents of human milk change in response to infant bronchiolitisBryan, D.; Hart, P.; Forsyth, K.; Gibson, R.
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.