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Results 1-10 of 14 (Search time: 0.006 seconds).
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PreviewIssue DateTitleAuthor(s)
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.
2009In Vitro Differentiation of Human Calvarial Suture Derived Cells With and Without Dexamethasione Does Not Induce In Vivo-Like ExpressionCoussens, A.; Hughes, I.; Morris, C.; Powell, B.; Anderson, P.
2009Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?Scheffer, I.; Zhang, Y.; Jansen, F.; Dibbens, L.
2009The frequency of molecular detection of virulence genes encoding cytolysin A, high-pathogenicity island and cytolethal distending toxin of Escherichia coli in cases of sudden infant death syndrome does not differ from that in other infant deaths and healthy infantsHighet, A.; Berry, A.; Bettelheim, K.; Goldwater, P.
2009Role of the multichannel intraluminal impedance technique in infants and childrenvan Wijk, M.; Benninga, M.; Omari, T.
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.
2009Novel hypothesis for unexplained sudden unexpected death in infancy (SUDI)Highet, A.; Berry, A.; Goldwater, P.
2009The NOURISH randomised control trial: Positive feeding practices and food preferences in early childhood - A primary prevention program for childhood obesityDaniels, L.; Magarey, A.; Battistutta, D.; Nicholson, J.; Farrell, A.; Davidson, G.; Cleghorn, G.
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.

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