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dc.creatorFretzayas, A.en
dc.creatorKitsiou, S.en
dc.creatorTsezou, A.en
dc.creatorAlexaki, A.en
dc.creatorNicolaidou, P.en
dc.date.accessioned2015-11-23T10:26:47Z
dc.date.available2015-11-23T10:26:47Z
dc.date.issued2006
dc.identifier10.1080/00365540500494087
dc.identifier.issn0036-5548
dc.identifier.urihttp://hdl.handle.net/11615/27575
dc.description.abstractWe describe 4 jaundiced neonates with acute pyelonephritis of whom family history was positive for or pointed to Gilbert's syndrome (GS). Uridine diphosphate glucuronosyltransferase 1A1 (UGT-1A1), ( TA) 7 polymorphism, associated with GS was found in these neonates. We suggest that extended ( TA) 7 promoter, acting as a predisposing factor, contributes substantially to hyperbilirubinaemia seen in a number of neonates with urinary tract infections (UTIs).en
dc.sourceScandinavian Journal of Infectious Diseasesen
dc.source.uri<Go to ISI>://WOS:000238562300023
dc.subjectURINARY-TRACT INFECTIONSen
dc.subjectBACTERIAL INFECTIONen
dc.subjectGILBERTS-SYNDROMEen
dc.subjectFEBRILE INFANTSen
dc.subjectBILIRUBIN LEVELen
dc.subjectJAUNDICEen
dc.subjectEXPRESSIONen
dc.subjectNEWBORNen
dc.subjectLIVERen
dc.subjectGENEen
dc.subjectInfectious Diseasesen
dc.titleUGT1A1 promoter polymorphism as a predisposing factor of hyperbilirubinaemia in neonates with acute pyelonephritisen
dc.typejournalArticleen


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