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Results 1-10 of 22 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
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.
2000
Saposins A,B,C, and D in plasma of patients with lysosomal storage disorders
Chang, M.
;
Bindloss, C.
;
Grabowski, G.
;
Qi, X.
;
Winchester, B.
;
Hopwood, J.
;
Meikle, P.
1998
Evaluation of the lysosome-associated membrane protein LAMP-2 as a marker for lysosomal storage disorders
Hua, C.
;
Hopwood, J.
;
Carlsson, S.
;
Harris, R.
;
Meikle, P.
2013
Short report: care for children and adolescents with diabetes in Australia and New Zealand: have we achieved the defined goals?
Cameron, F.
;
Cotterill, A.
;
Couper, J.
;
Craig, M.
;
Davis, E.
;
Donaghue, K.
;
Jones, T.
;
King, B.
;
Sheil, B.
2002
The molecular basis of cystathionine b-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatment
Gaustadnes, M.
;
Wilcken, B.
;
Oliveriusova, J.
;
McGill, J.
;
Fletcher, J.
;
Kraus, J.
;
Wilcken, D.
2010
Testicular and paratesticular pathology in children: a 12-year histopathological review
Marulaiah, M.
;
Gilhotra, A.
;
Moore, L.
;
Boucaut, H.
;
Goh, D.
2010
Chemokine/Chemokine receptor interactions in extramedullary leukaemia of the skin in childhood AML: Differential roles for CCR2, CCR5, CXCR4 and CXCR7
Faaij, C.
;
Willemze, A.
;
Revesz, T.
;
Balzarolo, M.
;
Tensen, C.
;
Hoogeboom, M.
;
Vermeer, M.
;
van Wering, E.
;
Zwaan, C.
;
Kaspers, G.
;
Story, C.
;
van Halteren, A.
;
Vossen, J.
;
Egeler, R.
;
van Tol, M.
;
Annels, N.
2000
Quantative histomorphometric analysis of the human growth plate from birth to adolescence
Byers, S.
;
Moore, A.
;
Byard, R.
;
Fazzalari, N.
2002
National study of adverse reactions after vaccination with bacille Calmette-Guérin
Turnbull, F.
;
McIntyre, P.
;
Achat, H.
;
Wang, H.
;
Stapledon, R.
;
Gold, M.
;
Burgess, M.
2007
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor
Ali, A.
;
Christie, P.
;
Grigorieva, I.
;
Harding, B.
;
Van Esch, H.
;
Ahmed, S.
;
Bitner-Glindzicz, M.
;
Blind, E.
;
Bloch, C.
;
Christin, P.
;
Clayton, P.
;
Gecz, J.
;
Gilbert-Dussardier, B.
;
Guillen-Navarro, E.
;
Hackett, A.
;
Halac, I.
;
Hendy, G.
;
Lalloo, F.
;
Mache, C.
;
Mughal, Z.
;
et al.
Discover
Author
2
et al.
2
Gold, M.
2
Hopwood, J.
2
Meikle, P.
2
Roberton, D.
1
Achat, H.
1
Ahmed, S.
1
Ali, A.
1
Anderson, P.
1
Anderson, P.J.
.
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Subject
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Child
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Humans
19
Infant
16
Female
16
Male
11
Adult
10
Australia
7
Middle Aged
3
Aged
3
Case-Control Studies
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Date issued
8
2010 - 2019
10
2000 - 2009
4
1995 - 1999