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Results 401-410 of 579 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2018Use of potentially inappropriate medications in people with dementia in Vietnam and its associated factorsNguyen, T.A.; Pham, T.; Vu, H.T.T.; Nguyen, T.X.; Vu, T.T.; Nguyen, B.T.T.; Nguyen, N.Q.; Nguyen, B.T.; Nguyen, T.N.; Phan, S.V.; Nguyen, A.T.; Pham, T.L.; Dang, H.T.; Kalisch-Ellett, L.; Gillam, M.; Pratt, N.; Qiang, S.; Wang, H.; Kanjanarach, T.; Hassali, M.A.A.; et al.
2018Germline genetic IKZF1 variation and predisposition to childhood acute lymphoblastic leukemiaChurchman, M.L.; Qian, M.; te Kronnie, G.; Zhang, R.; Yang, W.; Zhang, H.; Lana, T.; Tedrick, P.; Baskin, R.; Verbist, K.; Peters, J.L.; Devidas, M.; Larsen, E.; Moore, I.M.; Gu, Z.; Qu, C.; Yoshihara, H.; Porter, S.N.; Pruett-Miller, S.M.; Wu, G.; et al.
2015A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adultsPerez-Andreu, V.; Roberts, K.; Xu, H.; Smith, C.; Zhang, H.; Yang, W.; Harvey, R.; Payne-Turner, D.; Devidas, M.; Cheng, I.; Carroll, W.; Heerema, N.; Carroll, A.; Raetz, E.; Gastier-Foster, J.; Marcucci, G.; Bloomfield, C.; Mrozek, K.; Kohlschmidt, J.; Stock, W.; et al.
2014Mutations in the Human UBR1 Gene and the Associated Phenotypic SpectrumSukalo, M.; Fiedler, A.; Guzman, C.; Spranger, S.; Addor, M.; Mcheik, J.; Benavent, M.; Cobben, J.; Gillis, L.; Shealy, A.; Deshpande, C.; Bozorgmehr, B.; Everman, D.; Stattin, E.; Liebelt, J.; Keller, K.; Bertola, D.; van Karnebeek, C.; Bergmann, C.; Liu, Z.; et al.
2016Second cancer risk and late mortality in adult Australians receiving allogeneic hematopoietic stem cell transplantation: a population-based cohort studyVajdic, C.M.; Mayson, E.; Dodds, A.J.; O'Brien, T.; Wilcox, L.; Nivison-Smith, I.; Le Marsney, R.; Daniels, B.; Ashton, L.J.; Tan, J.; Bilmon, I.; Aarons, D.; Tran, S.; Gibson, J.; Johnston, A.; Greenwood, M.; Forbes, M.; Hertzberg, M.; Huang, G.; Spencer, A.; et al.
2015Autophagy in malignant transformation and cancer progressionGalluzzi, L.; Pietrocola, F.; Bravo-San Pedro, J.; Amaravadi, R.; Baehrecke, E.; Cecconi, F.; Codogno, P.; Debnath, J.; Gewirtz, D.; Karantza, V.; Kimmelman, A.; Kumar, S.; Levine, B.; Maiuri, M.; Martin, S.; Penninger, J.; Piacentini, M.; Rubinsztein, D.; Simon, H.; Simonsen, A.; et al.
2016Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypesMachiela, M.; Lan, Q.; Slager, S.; Vermeulen, R.; Teras, L.; Camp, N.; Cerhan, J.; Spinelli, J.; Wang, S.; Nieters, A.; Vijai, J.; Yeager, M.; Wang, Z.; Ghesquières, H.; McKay, J.; Conde, L.; de Bakker, P.; Cox, D.; Burdett, L.; Monnereau, A.; et al.
2012Outcome modeling with CRLF2, IKZF1, JAK and minimal residual disease in pediatric acute lymphoblastic leukemia: a Children's Oncology Group studyChen, I.; Harvey, R.; Mullighan, C.; Gastier-Foster, J.; Wharton, W.; Kang, H.; Borowitz, M.; Camitta, B.; Carroll, A.; Devidas, M.; Pullen, D.; Payne-Turner, D.; Tasian, S.; Reshmi, S.; Cottrell, C.; Reaman, G.; Bowman, W.; Carroll, W.; Loh, M.; Winick, N.; et al.
2012Risk factors to predict the incidence of surgical adverse events following open or laparoscopic surgery for apparent early stage endometrial cancer: results from a randomised controlled trialKondalsamy-Chennakesavan, S.; Janda, M.; Gebski, V.; Baker, J.; Brand, A.; Hogg, R.; Jobling, T.W.; Land, R.; Manolitsas, T.; Nascimento, M.; Neesham, D.; Nicklin, J.L.; Oehler, M.K.; Otton, G.; Perrin, L.; Salfinger, S.; Hammond, I.; Leung, Y.; Sykes, P.; Ngan, H.; et al.
2016Integration of genetic and clinical risk factors improves prognostication in relapsed childhood B-cell precursor acute lymphoblastic leukemiaIrving, J.; Enshaei, A.; Parker, C.; Sutton, R.; Kuiper, R.; Erhorn, A.; Minto, L.; Venn, N.; Law, T.; Yu, J.; Schwab, C.; Davies, R.; Matheson, E.; Davies, A.; Sonneveld, E.; Den Boer, M.; Love, S.; Harrison, C.; Hoogerbrugge, P.; Revesz, T.; et al.

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