Glucose-6-phosphate dehydrogenase deficiency and severe neonatal hyperbilirubinemia: a complexity of interactions between genes and environment
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference72 articles.
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1. Reply to Letter to the Editor–Glutathione S-transferase and moderate neonatal hyperbilirubinemia associated with glucose-6-phosphate dehydrogenase deficiency;The Journal of Pediatrics;2024-02
2. Vitamin K and Glucose-6-phosphate Dehydrogenase Deficiency: A Perspective;Annals of Pediatric Gastroenterology and Hepatology ISPGHAN;2023-10-18
3. Clinical performance validation of the STANDARD G6PD test: A multi-country pooled analysis;PLOS Neglected Tropical Diseases;2023-10-12
4. Grand Rounds Hyperbilirubinemia following Phototherapy in Glucose-6-Phosphate Dehydrogenase-Deficient Neonates: Not Out of the Woods;The Journal of Pediatrics;2023-10
5. The Genetics of Glucose-6-Phosphate-Dehydrogenase (G6PD) and Uridine Diphosphate Glucuronosyl Transferase 1A1 (UGT1A1) Promoter Gene Polymorphism in Relation to Quantitative Biochemical G6PD Activity Measurement and Neonatal Hyperbilirubinemia;Children;2023-07-06
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