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Results 21-30 of 77 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
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.
2006Intracellular cytokies in peripheral blood leucocytes in children with chronic renal failureNairn, J.; Hodge, G.; Henning, P.
2000Magnetic resonance imaging of growth plate injuries: the efficacy and indications for surgical proceduresFutami, T.; Foster, B.; Morris, L.; LeQuesne, G.
2005Changes in leukocyte subsets: clinical implications for children with chronic renal failureNairn, J.; Hodge, G.; Henning, P.
2004Genetic architecture of idiopathic generalized epilepsy: Clinical genetic analysis of 55 multiplex familiesMarini, C.; Scheffer, I.; Crossland, K.; Grinton, B.; Phillips, F.; McMahon, J.; Turner, S.; Dean, J.; Kivity, S.; Mazarib, A.; Neufeld, M.; Korczyn, A.; Harkin, L.; Dibbens, L.; Wallace, R.; Mulley, J.; Berkovic, S.
2008Folate, homocysteine, and candidate genes for vascular disease in children with type 1 diabetesCouper, J.; Pena Vargas, A.
2007Mutational analysis of mucopolysaccharidosis type VI patients undergoing a phase II trial of enzyme replacement therapyKarageorgos, L.; Brooks, D.; Harmatz, P.; Ketteridge, D.; Pollard, A.; Melville, E.; Parkinson-Lawrence, E.; Clements, P.; Hopwood, J.
2003Pharmacodynamics and dosing of aminoglycosidesTurnidge, J.
2002Urine amino and organic acids analysis in developmental delay or intellectual disabilityPoplawski, N.; Harrison, J.; Norton, W.; Wiltshire, E.; Fletcher, J.
2001Reduced total plasma homocyst(e)ine in children and adolescents with type 1 diabetesWiltshire, E.; Thomas, D.; Baghurst, P.; Couper, J.