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Results 1-10 of 37 (Search time: 0.003 seconds).
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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.
2020
Molecular patterns of response and treatment failure after frontline venetoclax combinations in older patients with AML
DiNardo, C.D.
;
Tiong, I.S.
;
Quaglieri, A.
;
MacRaild, S.
;
Loghavi, S.
;
Brown, F.C.
;
Thijssen, R.
;
Pomilio, G.
;
Ivey, A.
;
Salmon, J.
;
Glytsou, C.
;
Fleming, S.A.
;
Zhang, Q.
;
Ma, H.
;
Patel, K.P.
;
Kornblau, S.M.
;
Xu, Z.
;
Chua, C.C.
;
Chen, X.
;
Blombery, P.
;
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.
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.
2013
A phase 2 trial of ponatinib in Philadelphia chromosome-positive leukemias
Cortes, J.E.
;
Kim, D.W.
;
Pinilla-Ibarz, J.
;
Le Coutre, P.
;
Paquette, R.
;
Chuah, C.
;
Nicolini, F.E.
;
Apperley, J.F.
;
Khoury, H.J.
;
Talpaz, M.
;
DiPersio, J.
;
DeAngelo, D.J.
;
Abruzzese, E.
;
Rea, D.
;
Baccarani, M.
;
Müller, M.C.
;
Gambacorti-Passerini, C.
;
Wong, S.
;
Lustgarten, S.
;
Rivera, V.M.
;
et al.
2019
Chromosomal abnormalities and prognosis in NPM1-mutated acute myeloid leukemia: a pooled analysis of individual patient data from nine international cohorts
Angenendt, L.
;
Röllig, C.
;
Montesinos, P.
;
Martínez-Cuadrón, D.
;
Barragan, E.
;
García, R.
;
Botella, C.
;
Martínez, P.
;
Ravandi, F.
;
Kadia, T.
;
Kantarjian, H.M.
;
Cortes, J.
;
Juliusson, G.
;
Lazarevic, V.
;
Höglund, M.
;
Lehmann, S.
;
Recher, C.
;
Pigneux, A.
;
Bertoli, S.
;
Dumas, P.Y.
;
et al.
2020
An investigation of antihypertensive class, dementia, and cognitive decline
Peters, R.
;
Yasar, S.
;
Anderson, C.S.
;
Andrews, S.
;
Antikainen, R.
;
Arima, H.
;
Beckett, N.
;
Beer, J.C.
;
Bertens, A.S.
;
Booth, A.
;
van Boxtel, M.
;
Brayne, C.
;
Brodaty, H.
;
Carlson, M.C.
;
Chalmers, J.
;
Corrada, M.
;
DeKosky, S.
;
Derby, C.
;
Dixon, R.A.
;
Forette, F.
;
et al.
2020
Effect of intravenous tenecteplase dose on cerebral reperfusion before thrombectomy in patients with large vessel occlusion ischemic stroke: the EXTEND-IA TNK part 2 randomized clinical trial
Campbell, B.C.V.
;
Mitchell, P.J.
;
Churilov, L.
;
Yassi, N.
;
Kleinig, T.J.
;
Dowling, R.J.
;
Yan, B.
;
Bush, S.J.
;
Thijs, V.
;
Scroop, R.
;
Simpson, M.
;
Brooks, M.
;
Asadi, H.
;
Wu, T.Y.
;
Shah, D.G.
;
Wijeratne, T.
;
Zhao, H.
;
Alemseged, F.
;
Ng, F.
;
Bailey, P.
;
et al.
2014
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma
Gharahkhani, P.
;
Burdon, K.
;
Fogarty, R.
;
Sharma, S.
;
Hewitt, A.
;
Martin, S.
;
Law, M.
;
Cremin, K.
;
Bailey, J.
;
Loomis, S.
;
Pasquale, L.
;
Haines, J.
;
Hauser, M.
;
Viswanathan, A.
;
McGuffin, P.
;
Topouzis, F.
;
Foster, P.
;
Graham, S.
;
Casson, R.
;
Chehade, M.
;
et al.
2020
Causes of blindness and vision impairment in 2020 and trends over 30 years, and prevalence of avoidable blindness in relation to VISION 2020: the Right to Sight: an analysis for the Global Burden of Disease Study
Bourne, R.R.A.
;
Briant, P.S.
;
Flaxman, S.R.
;
Taylor, H.R.B.
;
Jonas, J.B.
;
Abdoli, A.A.
;
Abrha, W.A.
;
Abualhasan, A.
;
Abu-Gharbieh, E.G.
;
Adal, T.G.
;
Afshin, A.
;
Ahmadieh, H.
;
Alemayehu, W.
;
Alemzadeh, S.A.S.
;
Alfaar, A.S.
;
Alipour, V.
;
Androudi, S.
;
Arabloo, J.
;
Arditi, A.B.
;
Aregawi, B.B.
;
et al.
Discover
Author
4
Vos, T.
3
Anderson, H.
3
Andrews, K.
3
Feng, J.
3
Flaxman, A.
3
Phillips, K.
3
Shibuya, K.
2
Abdalla, S.
2
Aboyans, V.
2
Abraham, J.
.
next >
Subject
7
Mutation
6
Infant
6
Polymorphism, Single Nucleotide
6
Risk Factors
6
Treatment Outcome
5
Age Factors
5
Child
5
Child, Preschool
5
Cohort Studies
5
Global Health
.
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Date issued
5
2020 - 2021
27
2010 - 2019
5
2002 - 2009