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Results 21-30 of 128 (Search time: 0.005 seconds).
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PreviewIssue DateTitleAuthor(s)
2009Immobilisation versus immediate mobilisation after intrauterine insemination: randomised controlled trialCusters, I.; Flierman, P.; Maas, P.; Cox, T.; Van Dessel, T.; Gerards, M.; Mochtar, M.; Janssen, C.; van der Veen, F.; Mol, B.
2008The ESEP study: salpingostomy versus salpingectomy for tubal ectopic pregnancy; the impact on future fertility: A randomised controlled trialMol, F.; Strandell, A.; Jurkovic, D.; Yalcinkaya, T.; Verhoeve, H.; Koks, C.; van der Linden, P.; Graziosi, G.; Thurkow, A.; Hoek, A.; Hogstrom, L.; Klinte, I.; Nilsson, K.; van Mello, N.; Ankum, W.; van der Veen, F.; Mol, B.; Hajenius, P.
2009Adverse drug reactions to tocolytic treatment for preterm labour: prospective cohort studyde Heus, R.; Mol, B.; Erwich, J.; van Geijn, H.; Gyselaers, W.; Hanssens, M.; Harmark, L.; van Holsbeke, C.; Duvekot, J.; Schobben, F.; Wolf, H.; Visser, G.
2002The risk of mortality or cerebral palsy in twins: A collaborative population-based studyScher, A.; Petterson, B.; Blair, E.; Ellenberg, J.; Grether, J.; Haan, E.; Reddihough, D.; Yeargin-Allsopp, M.; Nelson, K.
2000Long-term effects of pyloromyotomy on pyloric motility and gastric emptying in humansSun, W.; Doran, S.; Jones, K.; Davidson, G.; Dent, J.; Horowitz, M.
2002Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutationTurner, G.; Partington, M.; Kerr, B.; Mangelsdorf, M.; Gecz, J.
2002Is there a relationship between Wolfram syndrome carrier status and suicide?Crawford, J.; Zielinski, M.; Fisher, L.; Sutherland, G.; Goldney, R.
2005Threshold effect of urinary glycosaminoglycans and the walk test as indicators of disease progression in a survey of subjects with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)Swiedler, S.; Beck, M.; Bajbouj, M.; Giugliani, R.; Schwartz, I.; Harmatz, P.; Wraith, J.; Roberts, J.; Ketteridge, D.; Hopwood, J.; Guffon, N.; Miranda, C.; Teles, E.; Berger, K.; Piscia-Nichols, C.
2006FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisitedAdes, L.; Sullivan, K.; Biggin, A.; Haan, E.; Brett, M.; Holman, K.; Dixon, J.; Robertson, S.; Holmes, A.; Rogers, J.; Bennetts, B.
2007Molecular consequences of dominant Bethlem myopathy collagen VI mutationsBaker, N.; Morgelin, M.; Pace, R.; Peat, R.; Adams, N.; Gardner, R.; Rowland, L.; Miller, G.; De Jonghe, P.; Ceulemans, B.; Hannibal, M.; Edwards, M.; Thompson, E.; Jacobson, R.; Quinlivan, R.; Aftimos, S.; Kornberg, A.; North, K.; Bateman, J.; Lamande, S.

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