1. Adelaide Research & Scholarship

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Results 1-10 of 20 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2009Determinants of mortality in non-neutropenic ICU patients with candidaemiaMarriott, D.; Playford, E.; Chen, S.; Slavin, M.; Nguyen, Q.; Ellis, D.; Sorrell, T.
2009Proton-pump inhibitors and the risk of antibiotic use and hospitalisation for pneumoniaRoughead, E.; Ramsay, E.; Pratt, N.; Ryan, P.; Gilbert, A.
2009Social and dental status along the life course and oral health impacts in adolescents: a population-based birth cohortGlazer De Anselmo Peres, K.; De Anselmo Peres, M.; Araujo, C.; Menezes, A.; Hallal, P.
2009Relationship between body adiposity measures and risk of primary knee and hip replacement for osteoarthritis: a prospective cohort studyWang, Y.; Simpson, J.A.; Wluka, A.E.; Teichtahl, A.J.; English, D.R.; Giles, G.G.; Graves, S.; Cicuttini, F.M.
2009Sequence variants in three loci influence monocyte counts and erythrocyte volumeFerreira, M.; Hottenga, J.; Warrington, N.; Medland, S.; Willemsen, G.; Lawrence, R.; Gordon, S.; de Geus, E.; Henders, A.; Smit, J.; Campbell, M.; Wallace, L.; Evans, D.; Wright, M.; Nyholt, D.; James, A.; Beilby, J.; Penninx, B.; Palmer, L.; Frazer, I.; et al.
2009Perinatal outcome of monoamniotic twin pregnanciesHack, K.; Derks, J.; Schaap, A.; Lopriore, E.; Elias, S.; Arabin, B.; Eggink, A.; Sollie, K.; Mol, B.; Duvekot, H.; Willekes, C.; Go, A.; Koopman-Esseboom, C.; Vandenbussche, F.; Visser, G.
2009The genomic basis of cerebral palsy: A HuGE systematic literature reviewO'Callaghan, M.; MacLennan, A.; Haan, E.; Dekker, G.
2009The presence and severity of chronic kidney disease predicts all-cause mortality in type 1 diabetesGroop, P.; Thomas, M.; Moran, J.; Waden, J.; Thorn, L.; Makinen, V.; Rosengard-Barlund, M.; Saraheimo, M.; Hietala, K.; Heikkia, O.; Forsblom, C.
2009Independent Association of HbA₁c and Incident Cardiovascular Disease in People Without DiabetesAdams, R.; Appleton, S.; Hill, C.; Wilson, D.; Taylor, A.; Chittleborough, C.; Gill, T.; Ruffin, R.
2009Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritanceDibbens, L.; Mullen, S.; Helbig, I.; Mefford, H.; Bayly, M.; Bellows, S.; Leu, C.; Trucks, H.; Obermeier, T.; Wittig, M.; Franke, A.; Caglayan, H.; Yapici, Z.; Sander, T.; Eichler, E.; Scheffer, I.; Mulley, J.; Berkovic, S.

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