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Results 1-10 of 37 (Search time: 0.006 seconds).
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PreviewIssue DateTitleAuthor(s)
2013The effect of maternal omega-3 (n-3) LCPUFA supplementation during pregnancy on early childhood cognitive and visual development: a systematic review and meta-analysis of randomized controlled trialsGould, J.; Smithers, L.; Makrides, M.
2013Learning from incident reports in the Australian medical imaging setting: handover and communication errorsHannaford, N.; Mandel, C.; Crock, C.; Buckley, K.; Magrabi, F.; Ong, M.; Allen, S.; Schultz, T.
2013Survival trends in pediatric in-hospital cardiac arrests: an analysis from get with the guidelines-resuscitationGirotra, S.; Spertus, J.A.; Li, Y.; Berg, R.A.; Nadkarni, V.M.; Chan, P.S.
2013Dietary n-3 LC-PUFA during the perinatal period as a strategy to minimize childhood allergic diseaseMakrides, M.; Gunaratne, A.; Collins, C.; Makrides, M.; Ochoa, J.; Szajewska, H.; The 77th NNI Workshop (28 Oct 2012 - 1 Nov 2012 : Panama City, FL)
2013Family matters: infants, toddlers and preschoolers of parents affected by mental illnessKowalenko, N.M.; Mares, S.P.; Newman, L.K.; Sved Williams, A.E.; Powrie, R.M.; van Doesum, K.T.M.
2013Short report: care for children and adolescents with diabetes in Australia and New Zealand: have we achieved the defined goals?Cameron, F.; Cotterill, A.; Couper, J.; Craig, M.; Davis, E.; Donaghue, K.; Jones, T.; King, B.; Sheil, B.
2013Modelling BMI trajectories in children for genetic association studiesWarrington, N.; Wu, Y.; Pennell, C.; Marsh, J.; Beilin, L.; Palmer, L.; Lye, S.; Briollais, L.; Wang, G.
2013Identification Of KLHL41 mutations implicates BTB-Kelch-Mediated Ubiquitination as an alternate pathway to myofibrillar disruption in nemaline myopathyGupta, V.; Ravenscroft, G.; Shaheen, R.; Todd, E.; Swanson, L.; Shiina, M.; Ogata, K.; Hsu, C.; Clarke, N.; Darras, B.; Farrar, M.; Hashem, A.; Manton, N.; Muntoni, F.; North, K.; Sandaradura, S.; Nishino, I.; Hayashi, Y.; Sewry, C.; Thompson, E.; et al.
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.
2013Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like featuresBonnefond, A.; Raimondo, A.; Stutzmann, F.; Ghoussaini, M.; Ramachandrappa, S.; Bersten, D.; Durand, E.; Vatin, V.; Balkau, B.; Lantieri, O.; Raverdy, V.; Pattou, F.; Van Hul, W.; Van Gaal, L.; Peet, D.; Weill, J.; Miller, J.; Horber, F.; Goldstone, A.; Driscoll, D.; et al.

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