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PreviewIssue DateTitleAuthor(s)
2012Gastroesophageal reflux in pediatrics: (patho)physiology and new insights in diagnostics and treatmentLoots, C.; Benninga, M.; Omari, T.
2010Complications of childhood diabetes and the role of technologyCho, Y.; Couper, J.; Donaghue, K.
2010The minimum frequency of glucose measurements from which glycemic variation can be consistently assessedBaghurst, P.; Rodbard, D.; Cameron, F.
2018Long-term academic functioning following cogmed working memory training for children born extremely preterm: a randomized controlled trialAnderson, P.J.; Lee, K.J.; Roberts, G.; Spencer-Smith, M.M.; Thompson, D.K.; Seal, M.L.; Nosarti, C.; Grehan, A.; Josev, E.K.; Gathercole, S.; Doyle, L.W.; Pascoe, L.
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)
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.
2018Maternal smoking during pregnancy and offspring overweight: is there a dose-response relationship? An individual patient data meta-analysisAlbers, L.; Sobotzki, C.; Kuß, O.; Ajslev, T.; Batista, R.; Bettiol, H.; Brabin, B.; Buka, S.; Cardoso, V.; Clifton, V.; Devereux, G.; Gilman, S.; Grzeskowiak, L.; Heinrich, J.; Hummel, S.; Jacobsen, G.; Jones, G.; Koshy, G.; Morgen, C.; Oken, E.; et al.
2015Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesisRamos-Brossier, M.; Montani, C.; Lebrun, N.; Gritti, L.; Martin, C.; Seminatore-Nole, C.; Toussaint, A.; Moreno, S.; Poirier, K.; Dorseuil, O.; Chelly, J.; Hackett, A.; Gecz, J.; Bieth, E.; Faudet, A.; Heron, D.; Kooy, R.; Loeys, B.; Humeau, Y.; Sala, C.; et al.
2016Prenatal fish oil supplementation and allergy: 6-year follow-up of a randomized controlled trialBest, K.P.; Sullivan, T.; Palmer, D.; Gold, M.; Kennedy, D.J.; Martin, J.; Makrides, M.
2016HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing studyFriez, M.; Brooks, S.; Stevenson, R.; Field, M.; Basehore, M.; Adès, L.; Sebold, C.; Mcgee, S.; Saxon, S.; Skinner, C.; Craig, M.; Murray, L.; Simensen, R.; Yap, Y.; Shaw, M.; Gardner, A.; Corbett, M.; Kumar, R.; Bosshard, M.; Van Loon, B.; et al.

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