1. Adelaide Research & Scholarship

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Results 21-30 of 42 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2009Oral health of teenage children in South AustraliaArmfield, J.
2009Reflux changes in adenoidal hyperplasia: a controlled prospective study to investigate its aetiologyHarris, P.; Hussey, D.; Watson, D.; Mayne, G.; Bradshaw, A.; Joniau, S.; Tan, L.; Wormald, P.; Carney, A.
2009Hospital admissions of Indigenous and non-Indigenous Australians due to interpersonal violence, July 1999 to June 2004Berry, J.; Harrison, J.; Ryan, P.
2009Sociodemographic correlates of food habits among school adolescents (12-15 year) in north Gaza StripAbudayya, A.; Stigum, H.; Shi, Z.; Abed, Y.; Holmboe-Ottesen, G.
2009Prevalence and causes of visual impairment in a Brazilian population: The Botucatu Eye StudySchellini, S.; Durkin, S.; Hoyama, E.; Hirai, F.; Cordeiro, R.; Casson, R.; Selva-Nayagam, D.; Padovani, C.
2009Thiopurine methyltransferase genetics is not a major risk factor for secondary malignant neoplasms after treatment of childhood acute lymphoblastic leukemia on Berlin-Frankfurt-Münster protocolsStanulla, M.; Schaeffeler, E.; Moricke, A.; Coulthard, S.; Cario, G.; Schrauder, A.; Kaatsch, P.; Dordelmann, M.; Welte, K.; Zimmerman, M.; Reiter, A.; Eichelbaum, M.; Riehm, H.; Schrappe, M.; Schwab, M.
2009Impact of childhood exposure to a natural disaster on adult mental health: 20-year longitudinal follow-up studyMcFarlane, A.; Van Hooff, M.
2009Collagen type III alpha 1 is a gastro-oesophageal reflux disease susceptibility gene and a male risk factor for hiatus herniaAsling, B.; Jirholt, J.; Hammond, P.; Knutsson, M.; Walentinsson, A.; Davidson, G.; Agreus, L.; Lehmann, A.; Lagerstrom-Fermer, M.
2009Cutaneous melanoma is related to immune suppression in kidney transplant recipientsVajdic, C.; van Leeuwen, M.; Webster, A.; McCredie, M.; Stewart, J.; Chapman, J.; Amin, J.; McDonald, S.; Grulich, A.
2009A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technologyTalseth-Palmer, B.; Bowden, N.; Meldrum, C.; Nicholl, J.; Thompson, E.; Friend, K.; Liebelt, J.; Bratkovic, D.; Haan, E.; Yu, S.; Scott, R.

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