1. Adelaide Research & Scholarship

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Results 1-10 of 30 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2008Tuberculosis: the dis-ease that didn't dis-appearBastian, I.; Krause, V.
2007Polysomnography in Australia-trends in provisionMarshall, N.; Wilsmore, B.; McEvoy, R.; Wheatley, J.; Dodd, M.; Grunstein, R.
2002A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotypeCundy, T.; Hegde, M.; Naot, D.; Chong, B.; King, A.; Wallace, R.; Mulley, J.; Love, D.; Seidel, J.; Fawkner, M.; Banovic, T.; Callon, K.; Grey, A.; Reid, I.; Middleton-Hardie, C.; Cornish, J.
2002Sodium-channel defects in benign familial neonatal-infantile seizuresHeron, S.; Crossland, K.; Andermann, E.; Phillips, H.; Hall, A.; Bleasel, A.; Shevell, M.; Mercho, S.; Seni, M.; Guiot, M.; Mulley, J.; Berkovic, S.; Scheffer, I.
2005A community-based intervention to reduce antibiotic use for upper respiratory tract infections in regional South AustraliaDollman, W.; LeBlanc, V.; Stevens, L.; O'Connor, P.; Turnidge, J.
2007Low CD4 T cell immunity to pneumolysin is associated with nasopharyngeal carriage of pneumococci in childrenZhang, Q.; Bagrade, L.; Bernatoniene, J.; Clarke, E.; Paton, J.; Mitchell, T.; Nunez, D.; Finn, A.
2023The effects of age and biological sex on the association between I-wave recruitment and the response to cTBS: an exploratory studyVan Dam, J.M.; Graetz, L.; Pitcher, J.B.; Goldsworthy, M.R.
2013Rare variants in single-minded 1 (SIM1) are associated with severe obesityRamachandrappa, S.; Raimondo, A.; Cali, A.; Keogh, J.; Henning, E.; Saeed, S.; Thompson, A.; Garg, S.; Bochukova, E.; Brage, S.; Trowse, V.; Wheeler, E.; Sullivan, A.; Dattani, M.; Clayton, P.; Datta, V.; Bruning, J.; Wareham, N.; O'Rahilly, S.; Peet, D.; et al.
2004Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathyBerkovic, S.; Heron, S.; Giordano, L.; Marini, C.; Guerrini, R.; Kaplan, R.; Gambardella, A.; Steinlein, O.; Grinton, B.; Dean, J.; Bordo, L.; Hodgson, B.; Yamamoto, T.; Mulley, J.; Zara, F.; Scheffer, I.
2003X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3Gedeon, A.; Nelson, J.; Gecz, J.; Mulley, J.

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