Search


Current filters:


Start a new search
Add filters:

Use filters to refine the search results.


Results 1-10 of 35 (Search time: 0.002 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
1995Exposure to environmental lead and visual motor integration at 7 years: The Port Pirie Cohort StudyBaghurst, P.; McMichael, A.; Tong, S.; Wigg, N.; Vimpani, G.; Robertson, E.
1995Haemolytic uraemic syndrome due to a Shiga-like toxin-producing Escherichia coli 048: H21 in South AustraliaGoldwater, P.; Bettelheim, K.
1998Transcranial correction of orbital neurofibromatosisSnyder, B.; Hanieh, A.; Trott, J.; David, D.
1995Adverse outcomes of bacterial meningitis in school aged survivorsGrimwood, K.; Anderson, V.; Bond, L.; Catroppa, C.; Hore, R.; Keir, E.; Nolan, T.; Roberton, D.
1998Asthma and other atopic diseases in Australian children. Australian arm of the International Study of Asthma and Allergy in ChildhoodRobertson, C.; Dalton, M.; Peat, J.; Haby, M.; Bauman, A.; Kennedy, J.; Landau, L.
1997A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeMuenke, M.; Gripp, K.; McDonald-McGinn, D.; Gaudenz, K.; Whitaker, L.; Bartlett, S.; Markowitz, R.; Robin, N.; Nwokoro, N.; Mulvihill, J.; Losken, H.; Mulliken, J.; Guttmacher, A.; Wilroy, R.; Clarke, L.; Hollway, G.; Ades, L.; Haan, E.; Mulley, J.; Cohen, M.; et al.
1998Haemolytic-uraemic syndrome outbreak caused by Escherichia coli O111:H-: clinical outcomesHenning, P.; Tham, E.; Martin, A.; Beare, T.; Jureidini, K.
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.
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.
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.