Associated Papers
Gilbert syndrome with systemic lupus erythematosus presenting with persistent unconjugated hyperbilirubinemia: A case report.
Ye N et al.
Experimental and Therapeutic Medicine, 2020
Combined Effects of UGT1A1 and SLCO1B1 Variants on Chinese Adult Mild Unconjugated Hyperbilirubinemia.
Bai J et al.
Frontiers in Genetics, 2019
Clinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia.
Yang H et al.
Pediatrics and Neonatology, 2016
Restriction fragment length polymorphism effectively identifies exon 1 mutation of UGT1A1 gene in patients with Gilbert's Syndrome.
Shiu TY et al.
Liver International : Official Journal of the International Association for the Study of the Liver, 2015
UGT1A1 gene variants and clinical risk factors modulate hyperbilirubinemia risk in newborns.
Tiwari PK et al.
Journal of Perinatology : Official Journal of the California Perinatal Association, 2014
Heme oxygenase-1 gene variants and hyperbilirubinemia risk in North Indian newborns.
Tiwari PK et al.
European Journal of Pediatrics, 2013
Risk factors associated with unconjugated neonatal hyperbilirubinemia in Malaysian neonates.
Wong F et al.
Journal of Tropical Pediatrics, 2013
Crigler-Najjar syndrome type 2.
Huang CS et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi, 2006
Select a paper to view details