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Results 81-87 of 87 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2017Adults with Philadelphia chromosome-like acute lymphoblastic leukemia frequently have IGH-CRLF2 and JAK2 mutations, persistence of minimal residual disease and poor prognosisHerold, T.; Schneider, S.; Metzeler, K.; Neumann, M.; Hartmann, L.; Roberts, K.; Konstandin, N.; Greif, P.; Braeundl, K.; Ksienzyk, B.; Huk, N.; Schneider, I.; Zellmeier, E.; Jurinovic, V.; Mansmann, U.; Hiddemann, W.; Mullighan, C.; Bohlander, S.; Spiekermann, K.; Hoelzer, D.; et al.
2015Global, regional, and national incidence, prevalence, and years lived with disability for 301 acute and chronic diseases and injuries in 188 countries, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013Global Burden of Disease Study 2013 Collaborators,; Vos, T.; Barber, R.; Bell, B.; Bertozzi-Villa, A.; Biryukov, S.; Bolliger, I.; Charlson, F.; Davis, A.; Degenhardt, L.; Dicker, D.; Duan, L.; Erskine, H.; Feigin, V.; Ferrari, A.; Fitzmaurice, C.; Fleming, T.; Graetz, N.; Guinovart, C.; Haagsma, J.; et al.
2022Youth-onset type 2 diabetes among First Nations young people in northern Australia: a retrospective, cross-sectional studyTitmuss, A.; Davis, E.A.; O'Donnell, V.; Wenitong, M.; Maple-Brown, L.J.; Haynes, A.; Barr, E.L.M.; Boffa, J.; Brown, A.D.H.; Connors, C.; Corpus, S.; Dowler, J.; Graham, S.; Griffiths, E.; Kirkham, R.; Lee, C.; Moore, E.; Pearson, G.; Shaw, J.E.; Singleton, S.; et al.
2022Microsatellite instability in young patients with rectal cancer: molecular findings and treatment responseZaborowski, A.M.; Abdile, A.; Adamina, M.; Aigner, F.; d'Allens, L.; Allmer, C.; Álvarez, A.; Anula, R.; Andric, M.; Atallah, S.; Bach, S.; Bala, M.; Barussaud, M.; Bausys, A.; Beggs, A.; Bellolio, F.; Bennett, M.-R.; Berdinskikh, A.; Bevan, V.; Biondo, S.; et al.
2023REVISE: Re-Evaluating the Inhibition of Stress Erosions in the ICU: a randomised trial protocolDeane, A.M.; Alhazzani, W.; Guyatt, G.; Finfer, S.; Marshall, J.C.; Myburgh, J.; Zytaruk, N.; Hardie, M.; Saunders, L.; Knowles, S.; Lauzier, F.; Chapman, M.J.; English, S.; Muscedere, J.; Arabi, Y.; Ostermann, M.; Venkatesh, B.; Young, P.; Thabane, L.; Billot, L.; et al.
2008Interferon autoantibodies associated with AIRE deficiency decrease the expression of IFN-stimulated genesKisand, K.; Link, M.; Wolff, A.; Meager, A.; Tserel, L.; Org, T.; Murumagi, A.; Uibo, R.; Willcox, N.; Podkrajek, K.; Battelino, T.; Lobell, A.; Kampe, O.; Lima, K.; Meloni, A.; Ergun-Longmire, B.; Maclaren, N.; Perheentupa, J.; Krohn, K.; Scott, H.; et al.
2019A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delayMucha, B.E.; Banka, S.; Ajeawung, N.F.; Molidperee, S.; Chen, G.G.; Koenig, M.K.; Adejumo, R.B.; Till, M.; Harbord, M.; Perrier, R.; Lemyre, E.; Boucher, R.M.; Skotko, B.G.; Waxler, J.L.; Thomas, M.A.; Hodge, J.C.; Gecz, J.; Nicholl, J.; McGregor, L.; Linden, T.; et al.

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