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Neonatal Screening for Glucose-6-Phosphate Dehydrogenase (G6PD) Gene Variants and Their Association With Hyperbilirubinemia and Phototherapy Needs. [PDF]
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Perinatal and Neonatal Outcomes in Infants of Diabetic Mothers: A Prospective Descriptive Study in a Tertiary Care Center in South India. [PDF]
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Neonatal Hyperbilirubinemia in Uganda: Mechanisms, Clinical Consequences, and Health-System Challenges. [PDF]
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Key role of Levitt's carbon monoxide breath test in revealing coexistent Gilbert syndrome and erythropoietic protoporphyria: A case report. [PDF]
World J Clin CasesKang LL, Zhang HD.
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Risk Factors and Clinical Outcomes of Glucose-6-Phosphate Dehydrogenase Deficiency in Neonates: A Case-Control Study. [PDF]
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Ursodeoxycholic Acid in the Management of Prolonged Neonatal Hyperbilirubinemia: A Randomized Controlled Clinical Trial. [PDF]
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Between Crigler-Najjar Syndrome Type II and Gilbert Syndrome: Expanding the Spectrum of Uridine Diphosphate Glucuronosyltransferase 1A1 (UGT1A1)-Related Hyperbilirubinemia. [PDF]
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Reducing Laboratory Testing and Blood Draws in the Newborn Nursery to Increase High-value Care. [PDF]
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