Prolonged Unconjugated Hyperbiliriubinemia in Breast-fed Male Infants with a Mutation of Uridine Diphosphate-Glucuronosyl Transferase
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference16 articles.
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3. Variations of the bilirubin uridine-diphosphoglucuronosyl transferase 1A1 gene in healthy Taiwanese;Huang;Pharmacogenetics,2000
4. Relationship between bilirubin UDP-glucuronosyltransferase 1A1 gene and neonatal hyperbilirubinemia;Huang;Pediatr Res,2002
5. Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyltransferase 1A1 gene, and neonatal hyperbilirubinemia;Huang;Gastroenterology,2002
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1. UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice;Frontiers in Pediatrics;2022-12-20
2. Bilirubin metabolism and UDP ‐glucuronosyltransferase 1A1 variants in Asians: Pathogenic implications and therapeutic response;The Kaohsiung Journal of Medical Sciences;2022-08
3. Prevalence and risk factors for hyperbilirubinemia among newborns from a low‐risk birth setting using delayed cord clamping in Japan;Japan Journal of Nursing Science;2020-08-16
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5. UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children;Medicine;2018-12
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