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Results 21-30 of 131 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1998Haemolytic-uraemic syndrome outbreak caused by Escherichia coli O111:H-: clinical outcomesHenning, P.; Tham, E.; Martin, A.; Beare, T.; Jureidini, K.
1999Homozygotes for FRA16B are normalHocking, T.; Feichtinger, W.; Schmid, M.; Haan, E.; Baker, E.; Sutherland, G.
1998X-linked adrenoleukodystrophy: the Australasian experienceKirk, E.; Fletcher, J.; Sharp, P.; Carey, B.; Poulos, A.
1996Differentiation of rare leukodystrophies by post-mortem morphological and biochemical studies: female adrenoleukodystrophy-like disease and late-onset Krabbe diseaseGullotta, F.; Hughes, J.; Wittkowski, W.; Poulos, A.; Strater, R.; Bernheimer, H.; Harzer, K.
1997Unbalanced t(4;11)(q32-q23) in a 34-year-old man with manifestations of distal monosomy 11q and trisomy 4q syndromesByatt, S.; Baker, E.; Richards, R.; Roberts, C.; Smith, A.
1998Identification of a human HECT family protein with homology to the Drosophila tumor suppressor gene hyperplastic discsCallaghan, M.; Russell, A.; Woollatt, E.; Sutherland, G.; Sutherland, R.; Watts, C.
1999Chronic recurrent multifocal osteomyelitis associated with chronic inflammatory bowel disease in childrenBousvaros, A.; Marcon, M.; Treem, W.; Waters, P.; Issenman, R.; Couper, R.; Burnell, R.; Rosenberg, A.; Rabinovich, E.; Kirschner, B.
1999Liver transplantation for citrullinaemia improves intellectual functionFletcher, J.; Couper, R.; Moore, D.; Coxon, R.; Dorney, S.
1998Identification of a common mutation (R245h) in Sanfilippo A patients from the NetherlandsWeber, B.; Vandekamp, J.; Kleijer, W.; Guo, X.H.; Blanch, L.; van Diggelen, O.; Wevers, R.; Poorthuis, B.; Hopwood, J.
1997Randomized, comparative trial of 20 micrograms vs 40 micrograms Engerix B vaccine in hepatitis B vaccine non-respondersGoldwater, P.