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PreviewIssue DateTitleAuthor(s)
2013Learning from incident reports in the Australian medical imaging setting: handover and communication errorsHannaford, N.; Mandel, C.; Crock, C.; Buckley, K.; Magrabi, F.; Ong, M.; Allen, S.; Schultz, T.
2013Appointment attendance at a remote rural dental training facility in AustraliaLalloo, R.; McDonald, J.
2013Erythrocyte-binding antigens of Plasmodium falciparum are targets of human inhibitory antibodies and function to evade naturally acquired immunityPersson, K.; Fowkes, F.; McCallum, F.; Gicheru, N.; Reiling, L.; Richards, J.; Wilson, D.; Lopaticki, S.; Cowman, A.; Marsh, K.; Beeson, J.
2013Enzyme replacement therapy for mucopolysaccharidosis VI: long-term cardiac effects of galsulfase (Naglazyme®) therapyBraunlin, E.; Rosenfeld, H.; Kampmann, C.; Johnson, J.; Beck, M.; Giugliani, R.; Guffon, N.; Ketteridge, D.; Miranda, C.; Scarpa, M.; Schwartz, I.; Teles, E.; Wraith, J.; Barrios, P.; Dias da Silva, E.; Kurio, G.; Richardson, M.; Gildengorin, G.; Hopwood, J.; Imperiale, M.; et al.
2013Childhood maltreatment is associated with an automatic negative emotion processing bias in the amygdalaDannlowski, U.; Kugel, H.; Huber, F.; Stuhrmann, A.; Redlich, R.; Grotegerd, D.; Dohm, K.; Sehlmeyer, C.; Konrad, C.; Baune, B.; Arolt, V.; Heindel, W.; Zwitserlood, P.; Suslow, T.
2013Changes in socioeconomic inequality in Indonesian children's cognitive function from 2000 to 2007: a decomposition analysisMaika, A.; Mittinty, N.; Brinkman, S.; Harper, S.; Satriawan, E.; Lynch, J.; Lidzba, K.
2013Cause-specific mortality and 30-year relative survival of Crohn's disease and ulcerative colitisSelinger, C.; Andrews, J.; Dent, O.; Norton, I.; Jones, B.; McDonald, C.; Cowlishaw, J.; Barr, G.; Selby, W.; Leong, R.
2013Diet quality of UK infants is associated with dietary, adiposity, cardiovascular, and cognitive outcomes measured at 7-8 years of ageGolley, R.; Smithers, L.; Mittinty, N.; Emmett, P.; Northstone, K.; Lynch, J.
2013Phenotype and genotype in 101 males with X-linked creatine transporter deficiencyvan de Kamp, J.; Bratkovic, D.; Poplawski, N.
2013Mutations in DEPDC5 cause familial focal epilepsy with variable fociDibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al.