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Results 31-40 of 128 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2002The molecular basis of cystathionine b-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatmentGaustadnes, M.; Wilcken, B.; Oliveriusova, J.; McGill, J.; Fletcher, J.; Kraus, J.; Wilcken, D.
2008Monocyte and macrophage killing of Helicobacter pylori: Relationship to bacterial virulence factorsBorlace, G.; Butler, R.; Brooks, D.
2009Induction of labour versus expectant monitoring for gestational hypertension or mild pre-eclampsia after 36 weeks' gestation (HYPITAT): a multicentre, open-label randomised controlled trialKoopmans, C.; Bijlenga, D.; Groen, H.; Vijgen, S.; Aarnoudse, J.; Bekedam, D.; van den Berg, P.; de Boer, K.; Burggraaff, J.; Bloemenkamp, K.; Drogtrop, A.; Franx, A.; de Groot, C.; Huisjes, A.; Kwee, A.; van Loon, A.; Lub, A.; Papatsonis, D.; van der Post, J.; Roumen, F.; et al.
2006A pilot study of the safety implications of Australian nurses' sleep and work hoursDorrian, J.; Lamond, N.; van den Heuvel, C.; Pincombe, J.; Rogers, A.; Drew, D.
2005Erythromycin dose of 70 mg accelerates gastric emptying as effectively as 200 mg in the critically illRitz, M.; Chapman, M.; Fraser, R.; Finnis, M.; Butler, R.; Cmielewski, P.; Davidson, G.; Rea, D.
2008Oligosaccharyltransferase-Subunit Mutations in Nonsyndromic Mental RetardationMolinari, F.; Foulquier, F.; Tarpey, P.; Morelle, W.; Boissel, S.; Teague, J.; Edkins, S.; Futreal, P.; Stratton, M.; Turner, G.; Matthijs, G.; Gecz, J.; Munnich, A.; Colleaux, L.
2005Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriersChenevix-Trench, G.; Sinilnikova, O.; Suthers, G.; Pandeya, N.; Mazoyer, S.; Sambrook, J.; Goldup, S.; Goldgar, D.; Lynch, H.; Lenoir, G.; Cheetham, G.
2008Maternal and cord plasma cytokine and chemokine profile in pregnancies complicated by asthmaOsei-Kumah, A.; Smith, R.; Clifton, V.
2008SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndromeGilfillan, G.; Selmer, K.; Roxrud, I.; Smith, R.; Kyllerman, M.; Eiklid, K.; Kroken, M.; Mattingsdal, M.; Egeland, T.; Stenmark, H.; Sjoholm, H.; Server, A.; Samuelsson, L.; Christianson, A.; Tarpey, P.; Whibley, A.; Stratton, M.; Futreal, P.; Teague, J.; Edkins, S.; et al.
2004Genetic architecture of idiopathic generalized epilepsy: Clinical genetic analysis of 55 multiplex familiesMarini, C.; Scheffer, I.; Crossland, K.; Grinton, B.; Phillips, F.; McMahon, J.; Turner, S.; Dean, J.; Kivity, S.; Mazarib, A.; Neufeld, M.; Korczyn, A.; Harkin, L.; Dibbens, L.; Wallace, R.; Mulley, J.; Berkovic, S.

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