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Results 21-30 of 366 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2017Does early-life family income influence later dental pain experience? A prospective 14-year studyGhorbani, Z.; Peres, M.; Liu, P.; Mejia, G.; Armfield, J.; Peres, K.
2018How are we assessing the safety and quality use of medicines used by young people in Australia?Bell, J.; Wilson, A.; Elshaug, A.; Nassar, N.
2019Influenza in Children With Special Risk Medical Conditions: A Systematic Review and Meta-analysisTuckerman, J.; Misan, S.; Crawford, N.W.; Marshall, H.S.
2019Parental offending and children’s emergency department presentations in New South Wales, AustraliaWhitten, T.; Green, M.; Laurens, K.; Tzoumakis, S.; Harris, F.; Carr, V.; Dean, K.
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.
2019Clinical indicators for common paediatric conditions: processes, provenance and products of the CareTrack Kids studyWiles, L.K.; Hooper, T.D.; Hibbert, P.D.; Molloy, C.; White, L.; Jaffe, A.; Cowell, C.T.; Harris, M.F.; Runciman, W.B.; Schmiede, A.; Dalton, C.; Hallahan, A.R.; Dalton, S.; Williams, H.; Wheaton, G.; Murphy, E.; Braithwaite, J.; Loeffen, E.
2019GJB2 and GJB6 mutations in hereditary recessive non-syndromic hearing impairment in CameroonTingang Wonkam, E.; Chimusa, E.; Noubiap, J.J.; Adadey, S.M.; F Fokouo, J.V.; Wonkam, A.
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.
2018Long-term academic functioning following cogmed working memory training for children born extremely preterm: a randomized controlled trialAnderson, P.J.; Lee, K.J.; Roberts, G.; Spencer-Smith, M.M.; Thompson, D.K.; Seal, M.L.; Nosarti, C.; Grehan, A.; Josev, E.K.; Gathercole, S.; Doyle, L.W.; Pascoe, L.
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.