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PreviewIssue DateTitleAuthor(s)
2019Mapping the PedsQL™ onto the CHU9D: an assessment of external validity in a large community-based sampleMpundu-Kaambwa, C.; Chen, G.; Huynh, E.; Russo, R.; Ratcliffe, J.
2019Association of modifiable risk factors with dental caries among Indigenous and Nonindigenous children in AustraliaJu, X.; Do, L.; Ha, D.; Jamieson, L.
2019Assessing the appropriateness of the management of upper respiratory tract infection in Australian children: a population-based sample surveyLong, J.C.; Williams, H.M.; Jani, S.; Arnolda, G.; Ting, H.P.; Molloy, C.J.; Hibbert, P.D.; Churruca, K.; Ellis, L.A.; Braithwaite, J.
2019Regulatory roles of IL-10-producing human follicular T cellsCañete, P.F.; Sweet, R.A.; Gonzalez-Figueroa, P.; Papa, I.; Ohkura, N.; Bolton, H.; Roco, J.A.; Cuenca, M.; Bassett, K.J.; Sayin, I.; Barry, E.; Lopez, A.; Canaday, D.H.; Meyer-Hermann, M.; Doglioni, C.; Fazekas de St Groth, B.; Sakaguchi, S.; Cook, M.C.; Vinuesa, C.G.
2019The influence of parental offending on the continuity and discontinuity of children’s internalizing and externalizing difficulties from early to middle childhoodWhitten, T.; Laurens, K.; Tzoumakis, S.; Kaggodaarachchi, S.; Green, M.; Harris, F.; Carr, V.; Dean, K.
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.