1. Adelaide Research & Scholarship

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Results 1-10 of 13 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1998Coexistence of Gaucher-Disease Type 1 and Joubert-SyndromeVan Royen-Kerkhof, A.; Pollthe, B.; Kleijer, W.; van Diggelen, O.; Aerts, J.; Hopwood, J.; Beemer, F.
1998Transcranial correction of orbital neurofibromatosisSnyder, B.; Hanieh, A.; Trott, J.; David, D.
1998Haemolytic-uraemic syndrome outbreak caused by Escherichia coli O111:H-: clinical outcomesHenning, P.; Tham, E.; Martin, A.; Beare, T.; Jureidini, K.
1998Declining blood lead levels and changes in cognitive function during childhood - The Port Pirie Cohort StudyTong, S.; Baghurst, P.; Sawyer, M.; Burns, J.; McMichael, A.
1998Evaluation of the lysosome-associated membrane protein LAMP-2 as a marker for lysosomal storage disordersHua, C.; Hopwood, J.; Carlsson, S.; Harris, R.; Meikle, P.
1998Focal foveolar cell hyperplasia presenting as recurrent emesis in a young infantMaster, V.; Davidson, G.; Morris, L.; Martin, J.; Kennedy, D.; Byard, R.; Freeman, J.
1998Bowel dysfunction in cystic fibrosis: importance of breath testingLewindon, P.; Robb, T.; Moore, D.; Davidson, G.; Martin, A.
1998Interleukin 2 receptor regulation and IL-2 function in the human infantZola, H.; Ridings, J.; Elliott, S.; Nobbs, S.; Weedon, H.; Wheatland, L.; Haslam, R.; Roberton, D.; Macardle, P.
1998A new pineoblastoma cell line, PER-480, with der(10)t(10;17), der(16)t(1;16), & enhanced MYC expression in the absence of gene amplification.Kees, U.; Spagnolo, D.; Hallam, L.; Ford, J.; Ranford, P.; Baker, D.; Callen, D.; Biegel, J.
1998Somatic mutation of immunoglobulin V(H)6 genes in human infantsRidings, J.; Dinan, L.; Williams, R.; Roberton, D.; Zola, H.

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