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Showing results 1992 to 2011 of 3020 < previous   next >
PreviewIssue DateTitleAuthor(s)
2012Nosocomial vs community-acquired pandemic influenza A (H1N1) 2009: a nested case-control studyKhandaker, G.; Rashid, H.; Zurynski, Y.; Richmond, P.; Buttery, J.; Marshall, H.; Gold, M.; Walls, T.; Whitehead, B.; Elliott, E.; Booy, R.
2007Novel action of n-3 polyunsaturated fatty acids - Inhibition of arachidonic acid-induced increase in tumor necrosis factor receptor expression on neutrophils and a role for proteasesMoghaddami, N.; Irvine, J.; Gao, X.; Grover, P.; Costabile, M.; Hii, C.; Ferrante, A.
2008Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoformSharma, S.; Burdon, K.; Dave, A.; Jamieson, R.; Yaron, Y.; Billson, F.; van Maldergem, L.; Lorenz, B.; Gecz, J.; Craig, J.
2010Novel combination therapy for the eradication of Helicobacter pylori infection in a mouse modelTran, C.; Kritas, S.; Campbell, M.; Huynh, H.; Lee, S.; Butler, R.
2013Novel FOXP3 surrogate biomarkers on human TregBresatz, S.; Ang, G.; Eastaff-Leung, N.; Hill, D.; Pederson, S.; Grose, R.; Krumbiegel, D.; Zola, H.; Brown, C.; Sadlon, T.; Barry, S.C.; Australian Gastroenterology Week 2013 (7 Oct 2013 - 9 Oct 2013 : Melbourne, Vic.)
2010Novel genetic marker for dilated end stage oesophagus and oesophageal adenocarcinoma risk? Authors' responseAsling, B.; Jirholt, J.; Hammond, P.; Knutsson, M.; Walentinsson, A.; Davidson, G.; Agreus, L.; Lehmann, A.; Lagerstrom-Fermer, M.
2009Novel hypothesis for unexplained sudden unexpected death in infancy (SUDI)Highet, A.; Berry, A.; Goldwater, P.
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.
2012Novel melatonin-based treatments for major depressionJureidini, J.; Raven, M.
2009Novel mutation in KCNQ2 causing benign familial neonatal seizuresGoldberg-Stern, H.; Kaufmann, R.; Kivity, S.; Afawi, Z.; Heron, S.
1997Novel Mutations in Sanfilippo A Syndrome : Implications For Enzyme FunctionWeber, B.; Guo, X.H.; Wraith, J.; Cooper, A.; Kleijer, W.; Bunge, S.; Hopwood, J.
2002Novel PEX1 mutations and genotype-phenotype correlations in Australasian peroxisome biogenesis disorder patientsMaxwell, Megan A.; Allen, Tamara; Solly, Pamela B.; Svingen, Terje; Paton, Barbara Cleland; Crane, Denis I.
2003Novel PHF6 mutation p.D333del causes Borjeson-Forssman-Lehmann syndromeBaumstark, A.; Lower, K.; Sinkus, A.; Andriuskeveviciute, I.; Jurkeniene, L.; Gecz, J.; Just, W.
2010Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genesDimasi, D.; Chen, J.; Hewitt, A.; Klebe, S.; Davey, R.; Stirling, J.; Thompson, E.; Forbes, R.; Tan, T.; Savarirayan, R.; Mackey, D.; Healey, P.; Mitchell, P.; Burdon, K.; Craig, J.
2013Nurse perceptions of family home-visiting programmes in Australia and EnglandSawyer, M.; Barnes, J.; Frost, L.; Jeffs, D.; Bowering, K.; Lynch, J.
2003NutritionCouper, R.; Gallard, V.; Robinson, M.; Robertson, D.; Australia & New Zealand Medical and Surgical Gastrointestinal Week (2009 : Sydney, Australia)
2018Nutrition for the next generation: older children and adolescentsDas, J.K.; Lassi, Z.S.; Hoodbhoy, Z.; Abdus Salam, R.A.
2005Nutritional aspects of single cell oils: uses and applications of arachidonic acid and docosahexaenoicSinclair, A.; Attar-Bashi, N.; Jayasooriya, A.; Gibson, R.; Makrides, M.; Cohen, Z.; Ratledge, C.
2002Nutritional effect of including egg yolk in the weaning diet of breast-fed and formula-fed infants: a randomized controlled trialMakrides, M.; Hawkes, J.; Neuman, M.; Gibson, R.
2004Nxf and Fbxo33: novel seizure-responsive genes in miceFlood, W.; Moyer, R.; Tsykin, A.; Sutherland, G.; Koblar, S.