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Results 1-10 of 77 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1995Central nervous system imaging in Crouzon SyndromeProudman, T.; Clark, B.; Moore, M.; Abbott, A.; David, D.
1996Munchausen Syndrome by Proxy: Child Abuse in the Medical SystemDonald, T.; Jureidini, J.
2007Improving patient satisfaction through information provisionBilling, K.; Newland, H.; Selva-Nayagam, D.
2000Open invitation from the International Poverty and Health Network to all healthcare professionalsHeath, I.; Haines, A.; Glover, J.; Hetzel, D.
2016TBC1D24 genotype-phenotype correlationBalestrini, S.; Milh, M.; Castiglioni, C.; Lüthy, K.; Finelli, M.; Verstreken, P.; Cardon, A.; Stražišar, B.; Holder, J.; Lesca, G.; Mancardi, M.; Poulat, A.; Repetto, G.; Banka, S.; Bilo, L.; Birkeland, L.; Bosch, F.; Brockmann, K.; Cross, J.; Doummar, D.; et al.
1998Declining blood lead levels and changes in cognitive function during childhood - The Port Pirie Cohort StudyTong, S.; Baghurst, P.; Sawyer, M.; Burns, J.; McMichael, A.
2020Contemporary Incidence and Prevalence of Rheumatic Fever and Rheumatic Heart Disease in Australia Using Linked Data: The Case for Policy ChangeKatzenellenbogen, J.M.; Bond-Smith, D.; Seth, R.J.; Dempsey, K.; Cannon, J.; Stacey, I.; Wade, V.; de Klerk, N.; Greenland, M.; Sanfilippo, F.M.; Brown, A.; Carapetis, J.R.; Wyber, R.; Nedkoff, L.; Hung, J.; Bessarab, D.; Ralph, A.P.
2019Pathogenic abnormal splicing due to intronic deletions that induce biophysical space constraint for spliceosome assemblyBryen, S.J.; Joshi, H.; Evesson, F.J.; Girard, C.; Ghaoui, R.; Waddell, L.B.; Testa, A.C.; Cummings, B.; Arbuckle, S.; Graf, N.; Webster, R.; MacArthur, D.G.; Laing, N.G.; Davis, M.R.; Lührmann, R.; Cooper, S.T.
2021Diet quality trajectories and cardiovascular phenotypes/metabolic syndrome risk by 11-12 yearsKerr, J.A.; Liu, R.S.; Gasser, C.E.; Mensah, F.K.; Burgner, D.; Lycett, K.; Gillespie, A.N.; Juonala, M.; Clifford, S.A.; Olds, T.; Saffery, R.; Gold, L.; Liu, M.; Azzopardi, P.; Edwards, B.; Dwyer, T.; Wake, M.
2019Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesiaGorman, K.M.; Meyer, E.; Grozeva, D.; Spinelli, E.; McTague, A.; Sanchis-Juan, A.; Carss, K.J.; Bryant, E.; Reich, A.; Schneider, A.L.; Pressler, R.M.; Simpson, M.A.; Debelle, G.D.; Wassmer, E.; Morton, J.; Sieciechowicz, D.; Jan-Kamsteeg, E.; Paciorkowski, A.R.; King, M.D.; Cross, J.H.; et al.

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