1. Adelaide Research & Scholarship

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Results 41-50 of 58 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1999Functional lymphocyte immunophenotypes observed in thalassaemia and haemophilia patients receiving current blood product preparationsHodge, G.; Lloyd, J.; Hodge, S.; Story, C.; Han, P.
2005Enzyme replacement therapy for Gaucher disease in AustraliaGoldblatt, J.; Szer, J.; Fletcher, J.; McGill, J.; Rowell, J.; Wilson, M.
2005The Hunter-McAlpine syndrome results from duplication 5q35-qterHunter, A.; DuPont, B.; McLaughlin, M.; Hinton, L.; Baker, E.; Ades, L.; Haan, E.; Schwartz, C.
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.
2007Unravelling the molecular control of calvarial suture fusion in children with craniosynostosisCoussens, A.; Wilkinson, C.; Hughes, I.; Morris, C.; Van Daal, A.; Anderson, P.; Powell, B.
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.
2004Mutations of the mitochondrial ND1 gene as a cause of MELASKirby, D.; McFarland, R.; Ohtake, A.; Dunning, C.; Ryan, M.; Wilson, C.; Ketteridge, D.; Turnbull, D.; Thorburn, D.; Taylor, R.
2009A Novel Bocavirus Associated with Acute Gastroenteritis in Australian ChildrenArthur, J.; Higgins, G.; Davidson, G.; Givney, R.; Ratcliff, R.; Münger, K.
1997Power spectral analysis of heart rate variability in children and adolescents with IDDMWawryk, A.; Bates, D.; Couper, J.

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