Gilbert Syndrome

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20 free full text articles

1. Right-lobe liver transplant from donors with Gilbert syndrome.
2. Severe jaundice in two children with Kawasaki disease: a possible association with Gilbert syndrome.
3. Diagnosis and treatment difficulties in 18-year-old male patient with hereditary hemochromatosis, chronic hepatitis B, Gilbert syndrome and ulcerative colitis.
4. Prevalence of Gilbert syndrome in parents of neonates with pathologic indirect hyperbilirubinemia.
5. Combined effect of regulatory polymorphisms on transcription of UGT1A1 as a cause of Gilbert syndrome.
6. Gilbert syndrome in Iran, Fars Province.
7. Gilbert syndrome in the newborn.
8. Gilbert syndrome presenting in a young boy, confirmed by the rifampin test.
9. Gilbert syndrome and the development of antiretroviral therapy-associated hyperbilirubinemia: genetic screening is unnecessary.
10. The polymorphism c.-3279T>G in the phenobarbital-responsive enhancer module of the bilirubin UDP-glucuronosyltransferase gene is associated with Gilbert syndrome.
11. Use of fully denaturing HPLC for UGT1A1 genotyping in Gilbert syndrome.
12. Gilbert syndrome and the development of antiretroviral therapy-associated hyperbilirubinemia.
13. Melting temperature assay for a UGT1A gene variant in Gilbert syndrome.
14. Rapid method for detection of extra (TA) in the promoter of the bilirubin-UDP-glucuronosyl transferase 1 gene associated with Gilbert syndrome.
15. Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis.
16. Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert syndrome.
17. Contribution of the TATA-box genotype (Gilbert syndrome) to serum bilirubin concentrations in the Italian population.
18. Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia.
19. The role of reduced calorie intake test in diagnosing Gilbert syndrome--a case report.
20. Identifying the gilbert syndrome.