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Results 21-30 of 33 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2022Treatment patterns and frequency of key outcomes in acute severe asthma in children: A Paediatric Research in Emergency Departments International Collaborative (PREDICT) multicentre cohort studyCraig, S.; Powell, C.V.E.; Nixon, G.M.; Oakley, E.; Hort, J.; Armstrong, D.S.; Ranganathan, S.; Kochar, A.; Wilson, C.; George, S.; Phillips, N.; Furyk, J.; Lawton, B.; Borland, M.L.; O'Brien, S.; Neutze, J.; Lithgow, A.; Mitchell, C.; Watkins, N.; Brannigan, D.; et al.
2015Influence of light exposure during early life on the age of onset of bipolar disorderBauer, M.; Glenn, T.; Alda, M.; Andreassen, O.; Angelopoulos, E.; Ardau, R.; Baethge, C.; Bauer, R.; Baune, B.; Bellivier, F.; Belmaker, R.; Berk, M.; Bjella, T.; Bossini, L.; Bersudsky, Y.; Wo Cheung, E.; Conell, J.; Del Zompo, M.; Dodd, S.; Etain, B.; et al.
2016Multiplex families with epilepsy: success of clinical and molecular genetic characterizationAfawi, Z.; Oliver, K.L.; Kivity, S.; Mazarib, A.; Blatt, I.; Neufeld, M.Y.; Helbig, K.L.; Goldberg-Stern, H.; Misk, A.J.; Straussberg, R.; Walid, S.; Mahajnah, M.; Lerman-Sagie, T.; Ben-Zeev, B.; Kahana, E.; Masalha, R.; Kramer, U.; Ekstein, D.; Shorer, Z.; Wallace, R.H.; et al.
2010Fine-scale survey of X chromosome copy number variants and indels underlying intellectual disabilityWhibley, A.; Plagnol, V.; Tarpey, P.; Abidi, F.; Fullston, T.; Choma, M.; Boucher, C.; Shepherd, L.; Willatt, L.; Parkin, G.; Smith, R.; Futreal, P.; Shaw, M.; Boyle, J.; Licata, A.; Skinner, C.; Stevenson, R.; Turner, G.; Field, M.; Hackett, A.; et al.
2013Mutations in DEPDC5 cause familial focal epilepsy with variable fociDibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; 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.
2006The effect of modifiable risk factors on pancreatic cancer mortality in populations of the Asia-Pacific regionAnsary-Moghaddam, A.; Huxley, R.; Barzi, F.; Lawes, C.; Ohkubo, T.; Fang, X.; Jee, S.; Woodward, M.; Okayama, A.; Ueshima, H.; Maegawa, H.; Aoki, N.; Nakamura, M.; Kubo, N.; Yamada, T.; Wu, Z.; Yao, C.; Andrews, G.; Welborn, T.; Tang, Z.; et al.
2011Genomewide association scan of suicidal thoughts and behaviour in major depressionSchosser, A.; Butler, A.; Ising, M.; Perroud, N.; Uher, R.; Ng, M.; Cohen-Woods, S.; Craddock, N.; Owen, M.; Korszun, A.; Jones, L.; Jones, I.; Gill, M.; Rice, J.; Maier, W.; Mors, O.; Rietschel, M.; Lucae, S.; Binder, E.; Preisig, M.; et al.; Domschke, K.
2010Global levels of specific histone modifications and an epigenetic gene signature predict prostate cancer progression and developmentBianco-Miotto, T.; Chiam, K.; Buchanan, G.; Jindal, S.; Day, T.; Thomas, M.; Pickering, M.; O'Loughlin, M.; Ryan, N.; Raymond, W.; Horvath, L.; Kench, J.; Stricker, P.; Marshall, V.; Sutherland, R.; Henshall, S.; Gerald, W.; Scher, H.; Risbridger, G.; Clements, J.; et al.
2021Early outcomes and complications following cardiac surgery in patients testing positive for coronavirus disease 2019: An international cohort studyAkowuah, E.; Benson, R.A.; Caruana, E.J.; Chetty, G.; Edwards, J.; Forlani, S.; Gradinariu, G.; Murphy, G.J.; Oo, A.Y.; Patel, A.J.; Ridley, B.; Rogers, L.J.; Sanders, J.; Tyson, N.; Vaja, R.; Siaw-Acheampong, K.; Argus, L.; Chaudhry, D.; Dawson, B.E.; Glasbey, J.C.; et al.

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