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Results 301-310 of 335 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2018Augmented capacity for peripheral serotonin release in human obesityYoung, R.; Lumsden, A.; Martin, A.; Schober, G.; Pezos, N.; Thazhath, S.; Isaacs, N.; Cvijanovic, N.; Sun, E.; Wu, T.; Rayner, C.; Nguyen, Q.N.; Fontgalland, D.; Rabbitt, P.; Hollington, P.; Sposato, L.; Due, S.; Wattchow, D.; Liou, A.; Jackson, V.; et al.
2016Association between transcatheter aortic valve replacement and subsequent infective endocarditis and in-hospital deathRegueiro, A.; Linke, A.; Latib, A.; Ihlemann, N.; Urena, M.; Walther, T.; Husser, O.; Herrmann, H.; Nombela-Franco, L.; Cheema, A.; Le Breton, H.; Stortecky, S.; Kapadia, S.; Bartorelli, A.; Sinning, J.; Amat-Santos, I.; Munoz-Garcia, A.; Lerakis, S.; Gutiérrez-Ibanes, E.; Abdel-Wahab, M.; et al.
2017Laparoscopy to predict the result of primary cytoreductive surgery in patients with advanced ovarian cancer: a randomized controlled trialRutten, M.; Van Meurs, H.; Van De Vrie, R.; Gaarenstroom, K.; Naaktgeboren, C.; Van Gorp, T.; Brugge, H.; Hofhuis, W.; Schreuder, H.; Arts, H.; Zusterzeel, P.; Pijnenborg, J.; Van Haaften, M.; Fons, G.; Engelen, M.; Boss, E.; Vos, M.; Gerestein, K.; Schutter, E.; Opmeer, B.; et al.
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.
2013SMAD2, SMAD3 and SMAD4 mutations in colorectal cancerFleming, N.; Jorissen, R.; Mouradov, D.; Christie, M.; Sakthianandeswaren, A.; Palmieri, M.; Day, F.; Li, S.; Tsui, C.; Lipton, L.; Desai, J.; Jones, I.; McLaughlin, S.; Ward, R.; Hawkins, N.; Ruszkiewicz, A.; Moore, J.; Zhu, H.; Mariadason, J.; Burgess, A.; et al.
2017Parallel palaeogenomic transects reveal complex genetic history of early European farmersLipson, M.; Szécsényi-Nagy, A.; Mallick, S.; Pósa, A.; Stégmár, B.; Keerl, V.; Rohland, N.; Stewardson, K.; Ferry, M.; Michel, M.; Oppenheimer, J.; Broomandkhoshbacht, N.; Harney, E.; Nordenfelt, S.; Llamas, B.; Gusztáv, B.; Köhler, K.; Oross, K.; Bondár, M.; Marton, T.; et al.
2006Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resourceMann, 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.
2017A mutation in the viral sensor 2’-5’-oligoadenylate synthetase 2 causes failure of lactationOakes, S.R.; Gallego-Ortega, D.; Stanford, P.M.; Junankar, S.; Au, W.W.Y.; Kikhtyak, Z.; von Korff, A.; Sergio, C.M.; Law, A.M.K.; Castillo, L.E.; Allerdice, S.L.; Young, A.I.J.; Piggin, C.; Whittle, B.; Bertram, E.; Naylor, M.J.; Roden, D.L.; Donovan, J.; Korennykh, A.; Goodnow, C.C.; et al.; Wells, C.A.
2018Congenital Titinopathy: Comprehensive characterization and pathogenic insightsOates, E.C.; Jones, K.J.; Donkervoort, S.; Charlton, A.; Brammah, S.; Smith, J.E.; Ware, J.S.; Yau, K.S.; Swanson, L.C.; Whiffin, N.; Peduto, A.J.; Bournazos, A.; Waddell, L.B.; Farrar, M.A.; Sampaio, H.A.; Teoh, H.L.; Lamont, P.J.; Mowat, D.; Fitzsimons, R.B.; Corbett, A.J.; et al.
2021Ursodeoxycholic acid in intrahepatic cholestasis of pregnancy: a systematic review and individual participant data meta-analysisOvadia, C.; Sajous, J.; Seed, P.T.; Patel, K.; Williamson, N.J.; Attilakos, G.; Azzaroli, F.; Bacq, Y.; Batsry, L.; Broom, K.; Brun-Furrer, R.; Bull, L.; Chambers, J.; Cui, Y.; Ding, M.; Dixon, P.H.; Estiú, M.C.; Gardiner, F.W.; Geenes, V.; Grymowicz, M.; et al.

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