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Results 1-7 of 7 (Search time: 0.004 seconds).
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Issue Date
Title
Author(s)
2014
Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing
Buchanan, D.
;
Tan, Y.
;
Walsh, M.
;
Clendenning, M.
;
Metcalf, A.
;
Ferguson, K.
;
Arnold, S.
;
Thompson, B.
;
Lose, F.
;
Parsons, M.
;
Walters, R.
;
Pearson, S.
;
Cummings, M.
;
Oehler, M.
;
Blomfield, P.
;
Quinn, M.
;
Kirk, J.
;
Stewart, C.
;
Obermair, A.
;
Young, J.
;
et al.
2021
Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility
Tudini, E.
;
Davidson, A.L.
;
Dressel, U.
;
Andrews, L.
;
Antill, Y.
;
Crook, A.
;
Field, M.
;
Gattas, M.
;
Harris, R.
;
Kirk, J.
;
Pachter, N.
;
Salmon, L.
;
Susman, R.
;
Townshend, S.
;
Trainer, A.H.
;
Tucker, K.M.
;
Mitchell, G.
;
James, P.A.
;
Ward, R.L.
;
Mar Fan, H.
;
et al.
2021
Prospective characterisation of SARS-CoV-2 infections among children presenting to tertiary paediatric hospitals across Australia in 2020: a national cohort study
Wurzel, D.
;
McMinn, A.
;
Hoq, M.
;
Blyth, C.C.
;
Burgner, D.
;
Tosif, S.
;
Buttery, J.
;
Carr, J.
;
Clark, J.E.
;
Cheng, A.C.
;
Dinsmore, N.
;
Francis, J.R.
;
Kynaston, A.
;
Lucas, R.
;
Marshall, H.
;
McMullan, B.
;
Singh-Grewal, D.
;
Wood, N.
;
Macartney, K.
;
Britton, P.N.
;
et al.
2003
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation
Burdon, K.
;
McKay, J.
;
Sale, M.
;
Russell-Eggitt, I.
;
Mackey, D.
;
Wirth, G.
;
Elder, J.
;
Nicoll, A.
;
Clarke, M.
;
FitzGerald, L.
;
Stankovich, J.
;
Shaw, M.
;
Sharma, S.
;
Gajovic, S.
;
Gruss, P.
;
Ross, S.
;
Thomas, P.
;
Voss, A.
;
Thomas, T.
;
Gecz, J.
;
et al.
2004
Phase 2 evaluation of parainfluenza type 3 cold passage mutant 45 live attenuated vaccine in healthy children 6-18 months old
Belshe, R.
;
Newman, F.
;
Tsai, T.
;
Karron, R.
;
Reisinger, K.
;
Roberton, D.
;
Marshall, H.
;
Schwartz, R.
;
King, J.
;
Henderson, F.
;
Rodriguez, W.
;
Severs, J.
;
Wright, P.
;
Keyserling, H.
;
Weinberg, G.
;
Bromberg, K.
;
Loh, R.
;
Sly, P.
;
McIntyre, P.
;
Ziegler, J.
;
et al.
2006
Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource
Mann, G.
;
Thorne, H.
;
Balleine, R.
;
Butow, P.
;
Clarke, C.
;
Edkins, E.
;
Evans, G.
;
Fereday, S.
;
Haan, E.
;
Gattas, M.
;
Giles, G.
;
Goldblatt, J.
;
Hopper, J.
;
Kirk, J.
;
Leary, J.
;
Lindeman, G.
;
Niedermayr, E.
;
Phillips, K.
;
Picken, S.
;
Pupo, G.
;
et al.
2022
Probiotic peanut oral immunotherapy versus oral immunotherapy and placebo in children with peanut allergy in Australia (PPOIT-003): a multicentre, randomised, phase 2b trial
Loke, P.
;
Orsini, F.
;
Lozinsky, A.C.
;
Gold, M.
;
O'Sullivan, M.D.
;
Quinn, P.
;
Lloyd, M.
;
Ashley, S.E.
;
Pitkin, S.
;
Axelrad, C.
;
Metcalfe, J.R.
;
Su, E.L.
;
Tey, D.
;
Robinson, M.N.
;
Allen, K.J.
;
Prescott, S.L.
;
Galvin, A.D.
;
Tang, M.L.K.
;
O'Sullivan, M.
;
Fahy-Scheer, S.
;
et al.
Discover
Author
3
Kirk, J.
2
Gattas, M.
2
Marshall, H.
1
Allen, K.J.
1
Andrews, L.
1
Antill, Y.
1
Arnold, S.
1
Ashley, S.E.
1
Axelrad, C.
1
Balleine, R.
.
next >
Subject
7
Humans
6
Female
4
Male
3
Cohort Studies
3
Germ-Line Mutation
3
Pedigree
2
Adult
2
Aged
2
Aged, 80 and over
2
Child
.
next >
Date issued
3
2020 - 2022
1
2010 - 2019
3
2003 - 2009