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Results 1-10 of 140 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2011FluCAN 2009: initial results from sentinel surveillance for adult influenza and pneumonia in eight Australian hospitalsKelly, P.; Kotsimbos, T.; Reynolds, A.; Wood-Baker, R.; Hancox, B.; Brown, S.; Holmes, M.; Simpson, G.; Bowler, S.; Waterer, G.; Irving, L.; Jenkins, C.; Thompson, P.; Cheng, A.
2010Self-injury in Australia: a community surveyMartin, G.; Swannell, S.; Hazell, P.; Harrison, J.; Taylor, A.
2010Enhanced liver fibrosis test can predict clinical outcomes in patients with chronic liver diseaseParkes, J.; Roderick, P.; Harris, S.; Day, C.; Mutimer, D.; Collier, J.; Lombard, M.; Alexander, G.; Ramage, J.; Dusheiko, G.; Wheatley, M.; Gough, C.; Burt, A.; Rosenberg, W.
2010Systematic care for asthma in Australian general practice: a randomised controlled trialHolton, C.; Beilby, J.; Harris, M.; Harper, C.; Proudfoot, J.; Ramsay, E.; Ruffin, R.
2015Neural crest cell-derived VEGF promotes embryonic jaw extensionWiszniak, S.; Mackenzie, F.E.; Anderson, P.; Kabbara, S.; Ruhrberg, C.; Schwarz, Q.
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.
2019Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2Corbett, M.A.; Kroes, T.; Veneziano, L.; Bennett, M.F.; Florian, R.; Schneider, A.L.; Coppola, A.; Licchetta, L.; Franceschetti, S.; Suppa, A.; Wenger, A.; Mei, D.; Pendziwiat, M.; Kaya, S.; Delledonne, M.; Straussberg, R.; Xumerle, L.; Regan, B.; Crompton, D.; van Rootselaar, A.-F.; et al.
2019Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmissionGuo, H.; Li, Y.; Shen, L.; Wang, T.; Jia, X.; Liu, L.; Xu, T.; Ou, M.; Hoekzema, K.; Wu, H.; Gillentine, M.A.; Liu, C.; Ni, H.; Peng, P.; Zhao, R.; Zhang, Y.; Phornphutkul, C.; Stegmann, A.P.A.; Prada, C.E.; Hopkin, R.J.; et al.
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.
2019Three pregnancies after transplantation: An 84-year-old kidney is the gift that keeps giving lifeBateman, S.M.; Coates, P.T.; Jesudason, S.