UGT1A1(∗)28 relationship with abnormal total bilirubin levels in chronic hepatitis C patients: Outcomes from a case–control study

Gilbert syndrome (GS) is a frequent benign clinical condition, marked by intermittent unconjugated hyperbilirubinemia, mostly due to the polymorphism uridine diphosphate-glucuronosyltransferase 1A1∗28 (UGT1A1∗28). Hyperbilirubinemia has been reported in a GS patient undergoing hepatitis C treatment,...

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Detalles Bibliográficos
Autores principales: de Souza, Marcelo Moreira Tavares, Vaisberg, Victor Van, Abreu, Rodrigo Martins, Ferreira, Aline Siqueira, daSilvaFerreira, Camila, Nasser, Paulo Dominguez, Paschoale, Helena Scavone, Carrilho, Flair José, Ono, Suzane Kioko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
4500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5369894/
https://www.ncbi.nlm.nih.gov/pubmed/28296739
http://dx.doi.org/10.1097/MD.0000000000006306

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5369894/
https://www.ncbi.nlm.nih.gov/pubmed/28296739
http://dx.doi.org/10.1097/MD.0000000000006306

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