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Results 81-90 of 585 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2017Is dimension order important when valuing health states using discrete choice experiments including duration?Mulhern, B.; Norman, R.; Lorgelly, P.; Lancsar, E.; Ratcliffe, J.; Brazier, J.; Viney, R.
2018Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working GroupHibar, D.; Westlye, L.; Doan, N.; Jahanshad, N.; Cheung, J.; Ching, C.; Versace, A.; Bilderbeck, A.; Uhlmann, A.; Mwangi, B.; Krämer, B.; Overs, B.; Hartberg, C.; Abé, C.; Dima, D.; Grotegerd, D.; Sprooten, E.; Bøen, E.; Jimenez, E.; Howells, F.; et al.
2020Contemporary Incidence and Prevalence of Rheumatic Fever and Rheumatic Heart Disease in Australia Using Linked Data: The Case for Policy ChangeKatzenellenbogen, J.M.; Bond-Smith, D.; Seth, R.J.; Dempsey, K.; Cannon, J.; Stacey, I.; Wade, V.; de Klerk, N.; Greenland, M.; Sanfilippo, F.M.; Brown, A.; Carapetis, J.R.; Wyber, R.; Nedkoff, L.; Hung, J.; Bessarab, D.; Ralph, A.P.
2017Expression patterns of HENMT1 and PIWIL1 in human testis: implications for transposon expressionHempfling, A.; Lim, S.; Adelson, D.; Evans, J.; O Connor, A.; Qu, Z.; Kliesch, S.; Weidner, W.; O Bryan, M.; Bergmann, M.
2007Health priorities and perceived health determinants among South Australians attending GLBTI festival eventsRogers, G.
2019Pathogenic abnormal splicing due to intronic deletions that induce biophysical space constraint for spliceosome assemblyBryen, S.J.; Joshi, H.; Evesson, F.J.; Girard, C.; Ghaoui, R.; Waddell, L.B.; Testa, A.C.; Cummings, B.; Arbuckle, S.; Graf, N.; Webster, R.; MacArthur, D.G.; Laing, N.G.; Davis, M.R.; Lührmann, R.; Cooper, S.T.
2002Suicide, gender, and age variations in India - are women in Indian society protected from suicide?Mayer, P.; Ziaian, T.
2020Coronavirus disease 2019 in patients with inborn errors of immunity: an international studyMeyts, I.; Bucciol, G.; Quinti, I.; Neven, B.; Fischer, A.; Seoane, E.; Lopez-Granados, E.; Gianelli, C.; Robles-Marhuenda, A.; Jeandel, P.Y.; Paillard, C.; Sankaran, V.G.; Demirdag, Y.Y.; Lougaris, V.; Aiuti, A.; Plebani, A.; Milito, C.; Dalm, V.A.; Guevara-Hoyer, K.; Sánchez-Ramón, S.; et al.
2019GJB2 and GJB6 mutations in hereditary recessive non-syndromic hearing impairment in CameroonTingang Wonkam, E.; Chimusa, E.; Noubiap, J.J.; Adadey, S.M.; F Fokouo, J.V.; Wonkam, A.
2019Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2Corbett, M.A.; Kroes, T.; Veneziano, L.; Bennett, M.F.; Florian, R.; Schneider, A.L.; Coppola, A.; Licchetta, L.; Franceschetti, S.; Suppa, A.; Wenger, A.; Mei, D.; Pendziwiat, M.; Kaya, S.; Delledonne, M.; Straussberg, R.; Xumerle, L.; Regan, B.; Crompton, D.; van Rootselaar, A.-F.; et al.

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