Molecular Diagnosis of a Familial Nonhemolytic Hyperbilirubinemia (Gilbert's Syndrome) in Healthy Subjects
Author:
Publisher
Wiley
Subject
Hepatology
Reference12 articles.
1. Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome
2. The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome
3. The Clinical Pharmacokinetics of the Newer Antiepileptic Drugs
4. Induction of zidovudine glucuronidation and amination pathways by rifampicin in HIV-infected patients
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2. Incidental Scleral Icterus in an Adolescent Male With Nausea: Clinical Diagnosis of Gilbert Syndrome in the Pediatric Outpatient Setting;Cureus;2023-08-10
3. Rapid detection of the irinotecan‐related UGT1A1 *28 polymorphism by asymmetric PCR melting curve analysis using one fluorescent probe;Journal of Clinical Laboratory Analysis;2022-06-29
4. Gilbert's Syndrome, Bilirubin Level and UGT1A1∗28 Genotype in Men of North-West Region of Russia;Journal of Clinical and Experimental Hepatology;2021-11
5. Gilbert Syndrome in a Young Ethiopian Man: First Case Report;Ethiopian Journal of Health Sciences;2021-01-01
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