1. Adelaide Research & Scholarship

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Results 1-10 of 15 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2009ASPREN surveillance system for influenza-like illness: a comparison with FluTracking and the National Notifiable Diseases Surveillance SystemParrella, A.; Dalton, C.B.; Pearce, R.; Litt, J.C.B.; Stocks, N.
2009Nontuberculous mycobacterial infection in children A prospective national studyBlyth, C.; Best, E.; Jones, C.; Nourse, C.; Goldwater, P.; Daley, A.; Burgner, D.; Henry, G.; Palasanthiran, P.
2009Preoperative use of ultrasonography to localize an ingested foreign bodyPiotto, L.; Gent, R.; Kirby, C.; Morris, L.
2009Role of the multichannel intraluminal impedance technique in infants and childrenvan Wijk, M.; Benninga, M.; Omari, T.
2009Risk factors and treatment for obstructive sleep apnea amongst obese children and adultsKohler, M.
2009Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2Ghalamkarpour, A.; Debauche, C.; Haan, E.; Van Regemorter, N.; Snzajer, Y.; Thomas, D.; Revencu, N.; Gillerot, Y.; Boon, L.; Vikkula, M.
2009Phases of diabetes in children and adolescentsCouper, J.; Donaghue, K.
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.
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.
2009SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotypeSpurlock, G.; Bennett, E.; Chuzhanova, N.; Thomas, N.; H-Ping, J.; Side, L.; Davies, S.; Haan, E.; Kerr, B.; Huson, S.; Upadhyaya, M.

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