Screening for Glucose-6-Phosphate Dehydrogenase Deficiency in Newborns—Practical Considerations
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference15 articles.
1. Glucose-6-phosphate dehydrogenase deficiency and severe neonatal hyperbilirubinemia: a complexity of interactions between genes and environment;Kaplan;Semin Fetal Neonatal Med,2010
2. Quantitative neonatal glucose-6-phosphate dehydrogenase screening: distribution, reference values and classification by phenotype;Algur;J Pediatr,2012
3. Glucose-6-phosphate dehydrogenase deficiency and borderline deficiency—association with neonatal hyperbilirubinemia;Riskin;J Pediatr,2012
4. The need for neonatal glucose-6-phosphate dehydrogenase screening: a global perspective;Kaplan;J Perinatol,2009
5. Implementation and analysis of a pilot in-hospital newborn screening program for glucose-6-phosphate dehydrogenase deficiency in the United States;Nock;J Perinatal,2011
Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Georacial Epidemiological Estimates of Glucose-6-Phosphate Dehydrogenase Deficiency among Newborns in the United States;American Journal of Perinatology;2023-04-27
2. Functional characterization of the p.(Gln195His) or Tainan and novel p.(Ser184Cys) or Toluca glucose-6-phosphate dehydrogenase (G6PD) gene natural variants identified through Mexican newborn screening for glucose-6-phosphate dehydrogenase deficiency;Clinical Biochemistry;2022-11
3. Economic evaluation of point of care universal newborn screening for glucose-6-Phosphate dehydrogenase deficiency in United States;The Journal of Maternal-Fetal & Neonatal Medicine;2021-02-24
4. Point-of-Care Testing for G6PD Deficiency: Opportunities for Screening;International Journal of Neonatal Screening;2018-11-19
5. Genotype–Phenotype Correlations of Glucose-6-Phosphate–Deficient Variants Throughout an Activity Distribution;The Journal of Applied Laboratory Medicine;2018-05-01
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