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Issue Date
Title
Author(s)
2019
Regulatory roles of IL-10-producing human follicular T cells
Cañete, 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.
2019
The influence of parental offending on the continuity and discontinuity of children’s internalizing and externalizing difficulties from early to middle childhood
Whitten, T.
;
Laurens, K.
;
Tzoumakis, S.
;
Kaggodaarachchi, S.
;
Green, M.
;
Harris, F.
;
Carr, V.
;
Dean, K.
2018
A review of preference-based measures for the assessment of quality of life in children and adolescents with cerebral palsy
Mpundu-Kaambwa, C.
;
Chen, G.
;
Huynh, E.
;
Russo, R.
;
Ratcliffe, J.
2017
Does early-life family income influence later dental pain experience? A prospective 14-year study
Ghorbani, Z.
;
Peres, M.
;
Liu, P.
;
Mejia, G.
;
Armfield, J.
;
Peres, K.
2018
How are we assessing the safety and quality use of medicines used by young people in Australia?
Bell, J.
;
Wilson, A.
;
Elshaug, A.
;
Nassar, N.
2019
Influenza in Children With Special Risk Medical Conditions: A Systematic Review and Meta-analysis
Tuckerman, J.
;
Misan, S.
;
Crawford, N.W.
;
Marshall, H.S.
2019
Parental offending and children’s emergency department presentations in New South Wales, Australia
Whitten, T.
;
Green, M.
;
Laurens, K.
;
Tzoumakis, S.
;
Harris, F.
;
Carr, V.
;
Dean, K.
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
Clinical indicators for common paediatric conditions: processes, provenance and products of the CareTrack Kids study
Wiles, 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.
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.
Discover
Author
47
et al.
24
Lynch, J.
23
Anderson, P.J.
19
Doyle, L.W.
17
Gecz, J.
13
Revesz, T.
10
Cheong, J.L.Y.
10
Lee, K.J.
9
Lawlor, D.
8
Chittleborough, C.
.
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Subject
366
Humans
270
Female
260
Male
206
Adolescent
184
Child, Preschool
130
Adult
114
Infant
97
Young Adult
78
Middle Aged
75
Australia
.
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Date issued
48
2019
25
2018
21
2017
30
2016
28
2015
37
2014
52
2013
46
2012
37
2011
56
2010
.
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