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Results 1-10 of 95 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2007Improving patient satisfaction through information provisionBilling, K.; Newland, H.; Selva-Nayagam, D.
2000Open invitation from the International Poverty and Health Network to all healthcare professionalsHeath, I.; Haines, A.; Glover, J.; Hetzel, D.
2008TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafnessGuipponi, M.; Antonarakis, S.; Scott, H.
2006Prevalence of trachoma among a group of Aboriginal school children in remote South AustraliaDurkin, S.; Casson, R.; Selva-Nayagam, D.; Newland, H.
2001Use of inhaled anti-inflammatory medication in children with asthma in managed care settingsAdams, R.; Fuhlbrigge, A.; Finkelstein, J.; Lozano, P.; Livingston, J.; Weiss, K.; Weiss, S.
2016TBC1D24 genotype-phenotype correlationBalestrini, S.; Milh, M.; Castiglioni, C.; Lüthy, K.; Finelli, M.; Verstreken, P.; Cardon, A.; Stražišar, B.; Holder, J.; Lesca, G.; Mancardi, M.; Poulat, A.; Repetto, G.; Banka, S.; Bilo, L.; Birkeland, L.; Bosch, F.; Brockmann, K.; Cross, J.; Doummar, D.; 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.
2023The unfinished agenda of communicable diseases among children and adolescents before the COVID-19 pandemic, 1990–2019: a systematic analysis of the Global Burden of Disease Study 2019Sharew, N.T.
2021Diet quality trajectories and cardiovascular phenotypes/metabolic syndrome risk by 11-12 yearsKerr, J.A.; Liu, R.S.; Gasser, C.E.; Mensah, F.K.; Burgner, D.; Lycett, K.; Gillespie, A.N.; Juonala, M.; Clifford, S.A.; Olds, T.; Saffery, R.; Gold, L.; Liu, M.; Azzopardi, P.; Edwards, B.; Dwyer, T.; Wake, M.
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.