Research graph
References from Uncommon Causes of Jaundice in a 16-Year-Old Girl. Local targets link to admitted publications; unresolved targets remain external evidence.
Hyperbilirubinemia in pediatrics: evaluation and care
2020 · External reference
Drug-induced liver injury in pediatrics
10.1097/mpg.0000000000003535 · 2022 · External reference
Azathioprine and 6-mercaptopurine-induced liver injury: clinical features and outcomes
10.1097/mcg.0000000000000568 · 2017 · External reference
Gilbert’s syndrome revisited
10.1016/j.jhep.2023.06.004 · 2023 · External reference
A rare case of Crigler-Najjar syndrome type 2: a case report and literature review
10.1002/ccr3.8176 · 2023 · External reference
Presence of the genetic marker for Gilbert syndrome is associated with increased level and duration of neonatal jaundice
10.1111/j.1651-2227.2002.tb01650.x · 2002 · External reference
Diagnostic criteria and contributors to Gilbert’s syndrome
10.1080/10408363.2018.1428526 · 2018 · External reference
Compound heterozygous UGT1A1*28 and UGT1A1*6 or single homozygous UGT1A1*28 are major genotypes associated with Gilbert’s syndrome in Chinese Han people
10.1016/j.gene.2021.145526 · 2021 · External reference
All you need to know about UGT1A1 genetic testing for patients treated with irinotecan: a practitioner-friendly guide
10.1200/op.21.00624 · 2022 · External reference
Gilbert’s syndrome: the good, the bad and the ugly
10.4254/wjh.v17.i2.98503 · 2025 · External reference
Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects
10.1016/j.bcmd.2012.01.004 · 2012 · External reference
Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II
10.1097/md.0000000000008620 · 2017 · External reference
Diagnosis and treatment of a 16-year-old Chinese patient with concurrent hereditary hemochromatosis and Gilbert’s syndrome
10.1186/s40001-014-0051-y · 2014 · External reference
Gilbert’s syndrome coexisting with hereditary spherocytosis might not be rare: Six case reports
10.12998/wjcc.v8.i10.2001 · 2020 · External reference
