1. Adelaide Research & Scholarship

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Results 1-10 of 17 (Search time: 0.001 seconds).
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PreviewIssue DateTitleAuthor(s)
2005Gastro-oesophageal reflux disease in infants and children: New insights, developments and old chestnutsOmari, T.
2003The detection of IgG antibodies to siliconeDewan, P.; Ashwood, P.; Rowan-Kelly, B.; Ferrante, A.; McCallum, Z.
2000Saposins A,B,C, and D in plasma of patients with lysosomal storage disordersChang, M.; Bindloss, C.; Grabowski, G.; Qi, X.; Winchester, B.; Hopwood, J.; Meikle, P.
2007Stressed mucosaDavidson, G.; Kritas, S.; Butler, R.; Cooke, R.J.; Vandenplas, Y.; Wahn, U.
2000Effects of birthweight and oxygen supplementation on lung function in late childhood in children of very low birth weightKennedy, J.; Edwards, L.; Bates, D.; Martin, A.; Nobbs, S.; Haslam, R.; McPhee, A.; Staugas, R.; Baghurst, P.
2002The molecular basis of cystathionine b-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatmentGaustadnes, M.; Wilcken, B.; Oliveriusova, J.; McGill, J.; Fletcher, J.; Kraus, J.; Wilcken, D.
2000Quantative histomorphometric analysis of the human growth plate from birth to adolescenceByers, S.; Moore, A.; Byard, R.; Fazzalari, N.
2002National study of adverse reactions after vaccination with bacille Calmette-GuérinTurnbull, F.; McIntyre, P.; Achat, H.; Wang, H.; Stapledon, R.; Gold, M.; Burgess, M.
2009Role of the multichannel intraluminal impedance technique in infants and childrenvan Wijk, M.; Benninga, M.; Omari, T.
2007Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factorAli, A.; Christie, P.; Grigorieva, I.; Harding, B.; Van Esch, H.; Ahmed, S.; Bitner-Glindzicz, M.; Blind, E.; Bloch, C.; Christin, P.; Clayton, P.; Gecz, J.; Gilbert-Dussardier, B.; Guillen-Navarro, E.; Hackett, A.; Halac, I.; Hendy, G.; Lalloo, F.; Mache, C.; Mughal, Z.; et al.

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