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Results 1-10 of 35 (Search time: 0.002 seconds).
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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.
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.
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.
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.
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.
2019Thirteen-year outcomes in very preterm children associated with diffuse excessive high signal intensity on neonatal magnetic resonance imagingMurner-Lavanchy, I.M.; Kidokoro, H.; Thompson, D.K.; Doyle, L.W.; Cheong, J.L.Y.; Hunt, R.W.; Inder, T.E.; Anderson, P.J.

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