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Results 21-30 of 108 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2000Saposins A,B,C, and D in plasma of patients with lysosomal storage disordersChang, M.; Bindloss, C.; Grabowski, G.; Qi, X.; Winchester, B.; Hopwood, J.; Meikle, P.
2001Depression among Australian adolescentsRey, J.; Sawyer, M.; Clark, J.; Baghurst, P.
2002Risk of death among cases attending South Australian major trauma services after severe trauma: the first 4 years of operation of a state trauma systemBrennan, P.; Everest, E.; Griggs, W.; Slater, A.; Carter, L.; Lee, C.; Semmens, J.; Wood, D.; Nguyen, A.; Owen, D.; Pilkington, P.; Roder, D.; Somers, R.
2006Effect of baclofen on esophagogastric motility and gastroesophageal reflux in children with gastroesophageal reflux disease: A randomized controlled trialOmari, T.; Benninga, M.; Sansom, L.; Butler, R.; Dent, J.; Davidson, G.
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.
2004Enzyme replacement therapy in mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome)Harmatz, P.; Whitley, C.; Waber, L.; Pais, R.; Steiner, R.; Plecko, B.; Kaplan, P.; Simon, J.; Butensky, E.; Hopwood, J.
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.
2004Twenty-two novel mutations in the lysosomal a-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type IIHermans, M.; van Leenen, D.; Kroos, M.; Beesley, C.; Van der Ploeg, A.; Sakuraba, H.; Wevers, R.; Kleijer, W.; Mikelakakis, H.; Kirk, E.; Fletcher, J.; Bosshard, N.; Basel-Vanagaite, L.; Besley, G.; Reuser, A.
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.

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