| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10163013 | Pediatria Polska | 2012 | 6 Pages |
Abstract
Identification of UGT1A1 gene polymorphism can explain the causes of neonate hiperbilirubinemia in children with no risk factors. Moreover it would allow individual treatment options. It would also be useful in patients' development as UDP-glucuronosyltransferase is engaged in metabolism of many widely used drugs. The performed analysis justify further UGT1A1 gene polymorphism studies in Polish population and can be useful in determination of an treatment algorithm for neonates suffering from hiperbilirubinemia.
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Authors
Katarzyna Ciach, Katarzyna Mazur, BogumiÅa KieÅbratowska, PrzemysÅaw Adamski, Beata Królikowska, MichaÅ Korzon, Krzysztof Preis, Krzysztof P. Bielawski,