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Results 1-10 of 46 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2019
Mapping the PedsQL™ onto the CHU9D: an assessment of external validity in a large community-based sample
Mpundu-Kaambwa, C.
;
Chen, G.
;
Huynh, E.
;
Russo, R.
;
Ratcliffe, J.
2019
Association of modifiable risk factors with dental caries among Indigenous and Nonindigenous children in Australia
Ju, X.
;
Do, L.
;
Ha, D.
;
Jamieson, L.
2019
Assessing the appropriateness of the management of upper respiratory tract infection in Australian children: a population-based sample survey
Long, 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.
2019
Effect of digital alteration information and disclaimer labels attached to fashion magazine advertisements on women's body dissatisfaction
Tiggemann, M.
;
Brown, Z.
;
Anderberg, I.
2019
Pathogenic abnormal splicing due to intronic deletions that induce biophysical space constraint for spliceosome assembly
Bryen, 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.
2019
GJB2 and GJB6 mutations in hereditary recessive non-syndromic hearing impairment in Cameroon
Tingang Wonkam, E.
;
Chimusa, E.
;
Noubiap, J.J.
;
Adadey, S.M.
;
F Fokouo, J.V.
;
Wonkam, A.
2019
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2
Corbett, 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.
2019
A randomised controlled trial of vaporised Δ⁹-tetrahydrocannabinol and cannabidiol alone and in combination in frequent and infrequent cannabis users: acute intoxication effects
Solowij, N.
;
Broyd, S.
;
Greenwood, L.M.
;
van Hell, H.
;
Martelozzo, D.
;
Rueb, K.
;
Todd, J.
;
Liu, Z.
;
Galettis, P.
;
Martin, J.
;
Murray, R.
;
Jones, A.
;
Michie, P.T.
;
Croft, R.
2019
Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission
Guo, 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.
2019
Thirteen-year outcomes in very preterm children associated with diffuse excessive high signal intensity on neonatal magnetic resonance imaging
Murner-Lavanchy, I.M.
;
Kidokoro, H.
;
Thompson, D.K.
;
Doyle, L.W.
;
Cheong, J.L.Y.
;
Hunt, R.W.
;
Inder, T.E.
;
Anderson, P.J.
Discover
Author
11
et al.
3
Beck, B.
3
Cameron, P.
3
Teague, W.
2
Anderson, P.J.
2
Avery, J.
2
Braaf, S.
2
Doyle, L.W.
2
Gabbe, B.
2
Gabbe, B.J.
.
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Subject
14
Aged
14
Australia
9
Infant, Newborn
6
Aged, 80 and over
6
Pedigree
5
Mutation
4
Incidence
4
Pregnancy
4
Prognosis
4
Registries
.
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