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Issue Date
Title
Author(s)
2002
Recombinant Human Bone Morphogenetic Protein-2 for Treatment of Open Tibial Fractures
Csimma, C.
;
Genant, H.
;
Valentin-Opran, A.
;
Amit, Y.
;
Arbel, R.
;
Aro, H.
;
Atar, D.
;
Bishay, M.
;
Borner, M.
;
Chiron, P.
;
Choong, P.
;
Cinats, J.
;
Courtenay, B.
;
Feibel, R.
;
Geulette, B.
;
Gravel, C.
;
Haas, N.
;
Raschke, M.
;
Hammacher, E.
;
van der Velde, D.
;
et al.
2018
Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group
Hibar, D.
;
Westlye, L.
;
Doan, N.
;
Jahanshad, N.
;
Cheung, J.
;
Ching, C.
;
Versace, A.
;
Bilderbeck, A.
;
Uhlmann, A.
;
Mwangi, B.
;
Krämer, B.
;
Overs, B.
;
Hartberg, C.
;
Abé, C.
;
Dima, D.
;
Grotegerd, D.
;
Sprooten, E.
;
Bøen, E.
;
Jimenez, E.
;
Howells, F.
;
et al.
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
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
Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia
Gorman, K.M.
;
Meyer, E.
;
Grozeva, D.
;
Spinelli, E.
;
McTague, A.
;
Sanchis-Juan, A.
;
Carss, K.J.
;
Bryant, E.
;
Reich, A.
;
Schneider, A.L.
;
Pressler, R.M.
;
Simpson, M.A.
;
Debelle, G.D.
;
Wassmer, E.
;
Morton, J.
;
Sieciechowicz, D.
;
Jan-Kamsteeg, E.
;
Paciorkowski, A.R.
;
King, M.D.
;
Cross, J.H.
;
et al.
2017
Developing consensus-based priority outcome domains for trials in kidney transplantation: a multinational Delphi Survey with patients, caregivers, and health professionals
Sautenet, B.
;
Tong, A.
;
Manera, K.
;
Chapman, J.
;
Warrens, A.
;
Rosenbloom, D.
;
Wong, G.
;
Gill, J.
;
Budde, K.
;
Rostaing, L.
;
Marson, L.
;
Josephson, M.
;
Reese, P.
;
Pruett, T.
;
Hanson, C.
;
O'Donoghue, D.
;
Tam-Tham, H.
;
Halimi, J.
;
Shen, J.
;
Kanellis, J.
;
et al.
2021
Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer
Singhal, D.
;
Hahn, C.N.
;
Feurstein, S.
;
Wee, L.Y.A.
;
Moma, L.
;
Kutyna, M.M.
;
Chhetri, R.
;
Eshraghi, L.
;
Schreiber, A.W.
;
Feng, J.
;
Wang, P.P.-S.
;
Babic, M.
;
Parker, W.T.
;
Gao, S.
;
Moore, S.
;
Das, S.
;
Thomas, D.
;
Pattnaik, S.
;
Brown, A.L.
;
D'Andrea, R.J.
;
et al.
2021
Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants
Whalen, S.
;
Shaw, M.
;
Mignot, C.
;
Héron, D.
;
Bastaraud, S.C.
;
Walti, C.C.
;
Liebelt, J.
;
Elmslie, F.
;
Yap, P.
;
Hurst, J.
;
Forsythe, E.
;
Kirmse, B.
;
Ozmore, J.
;
Spinelli, A.M.
;
Calabrese, O.
;
de Villemeur, T.B.
;
Tabet, A.C.
;
Levy, J.
;
Guet, A.
;
Kossorotoff, M.
;
et al.
2017
Electrophysiological, cognitive and clinical profiles of at-risk mental state: the longitudinal minds in transition (MinT) study
Atkinson, R.J.
;
Fulham, W.R.
;
Michie, P.T.
;
Ward, P.B.
;
Todd, J.
;
Stain, H.
;
Langdon, R.
;
Thienel, R.
;
Paulik, G.
;
Cooper, G.
;
Anthes, L.
;
Bowen, D.
;
Case, V.
;
Clark, S.
;
Collins-Langworthy, J.
;
Curtis, J.
;
Ehlkes, T.
;
Haddow, T.
;
Lawrence, C.
;
Logan, S.
;
et al.
;
Hashimoto, K.
2018
A four-gene lincRNA expression signature predicts risk in multiple cohorts of acute myeloid leukemia patients
Beck, D.
;
Thoms, J.
;
Palu, C.
;
Herold, T.
;
Shah, A.
;
Olivier, J.
;
Boelen, L.
;
Huang, Y.
;
Chacon, D.
;
Brown, A.
;
Babic, M.
;
Hahn, C.
;
Perugini, M.
;
Zhou, X.
;
Huntly, B.
;
Schwarzer, A.
;
Klusmann, J.-H.
;
Berdel, W.
;
Wörmann, B.
;
Büchner, T.
;
et al.
Discover
Author
3
Babic, M.
3
Barrett, H.
3
Branford, S.
3
Couper, J.
3
Donaghue, K.
2
Ambler, G.
2
Anderson, K.
2
Baccarani, M.
2
Baskerville, T.
2
Batch, J.
.
next >
Subject
10
Mutation
9
Aged, 80 and over
9
Infant
8
Prognosis
7
Australia
6
Risk Factors
5
Genetic Predisposition to Disease
5
Pedigree
5
Prospective Studies
5
Treatment Outcome
.
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Date issued
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2020 - 2023
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2010 - 2019
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2002 - 2009