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Congenital familial non-haemolytic hyperbilirubinaemias are potentially lethal syndromes caused by genetic lesions that reduce or abolish hepatic bilirubin UDP-glucuronosyltransferase activity. Here… (More)
Human gene families encoding UDP-Glucuronosyltransferases (UGTs) have been identified and partially characterised. This family of enzymes catalysed the glucuronidation of drugs, xenobiotics and… (More)
OBJECTIVE Prolonged neonatal jaundice, beyond day 14 of life, is very common and of concern to the clinician. The aim of this study was to investigate whether a genetic mutation in the bilirubin… (More)
1The primary or idiopathic dystonias are non-degenerative conditions where dystonia (with the possible exception of a coexistent tremor) is the only clinical abnormality. Within this group are the… (More)
R. Herbert, BSc, HDCR(R), DMS, Superintendent I Radiographer* V. T. McCollum, DCR(R), PGC(CT), Superintendent III Radiographer* A. Cassidy, DCR(R), MDCR, DMU, Superintendent III Radiographer* K. M.… (More)