REFERENCES
- Lazarus C, Avchen RN. Neonatal hyperbilirubinemia management: a model for change. J Perinatol. 2009;29(Suppl 1):S58–S60.
- Dors N, Rodrigues Pereira R, van Zwieten R, . Glucose-6-phosphate dehydrogenase deficiency: clinical presentation and eliciting factors. Ned Tijdschr Geneeskd. 2008;152:1029–1033.
- Tavazzi D, Taher A, Cappellini M. Red blood cell enzyme disorders: an overview. Pediatr Ann. 2008;37:303–310.
- Zanella A, Fermo E, Bianchi P, . Pyruvate kinase deficiency: the genotype-phenotype association. Blood Rev. 2007;21:217–231.
- American Academy of Pediatrics. Clinical Practice Guideline: Management of Hyperbilirubinemia in the Newborn Infant 35 or More Weeks of Gestation. Pediatrics. 2004;114:297–316.
- World Medical Association. Declaration of Helsinki. Ethical Principles for Medical Research Involving Human Subjects, the 59th WMA General Assembly, 2008, Seoul, South Korea.
- Brewer GJ, Tarlov AR, Alving AS. Methemoglobin reduction test: a new, simple, in vitro test for identifying primaquine-sensitivity. Bull World Health Organ. 1960;22:633–640.
- SPSS. Statistical Package for Social Science. Standard version 10.0.5. Chicago, IL: SPSS; 1999.
- Farez-Vidal ME, Gandia-Pla S, Blanco S, . Multi-mutational analysis of fifteen common mutations of the glucose 6-phosphate dehydrogenase gene in the Mediterranean population. Clin Chim Acta. 2008;395:94–98.
- Settin A, Al-Haggar M, Al-Raz R, . Screening for G6PD Mediterranean mutation among Egyptian neonates with high or prolonged jaundice. Haema. 2006;9:83–90.
- Atay E, Bozaykut A, Ipek IO. Glucose-6-phosphate dehydrogenase deficiency in neonatal indirect hyperbilirubinemia. J Trop Pediatr. 2006;52:56–58.
- Iranpour R, Akbar MR, Haghshenas I. Glucose-6-phosphate dehydrogenase deficiency in neonates. Indian J Pediatr. 2003;70:855–857.
- Doxiadis SA, Fessas PH, Valaes T, Mastrokalos N. Glucose-6-phosphate dehydrogenase deficiency: a new etiological factor of severe neonatal jaundice. Lancet. 1961;1:297–301.
- Al-Omran A, Al-Ghazal F, Gupta S, Thomas BJ. Glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice in Al-Hofuf area. Ann Saudi Med. 1999;19:130–135.
- Weng Y, Chou Y, Lien R. Hyperbilirubinemia in healthy neonates with glucose-6-phosphate dehydrogenase deficiency. Early Human Dev. 2003;71:129–136.
- Kaplan M, Beutler E, Vreman HJ, . Neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes. Pediatrics. 1999;104:68–74.
- Beutler E. G6PD deficiency. Blood. 1994;84:3613–3636.
- Valaes T. Severe neonatal jaundice associated with glucose-6-phosphate dehydrogenase deficiency: pathogenesis and global epidemiology. Acta Paediatr Suppl. 1994;394:58–76.
- Kaplan M, Vreman HJ, Hammerman C, . Combination of ABO blood group incompatibility and glucose-6-phosphate dehydrogenase deficiency: effect on hemolysis and neonatal hyperbilirubinemia. Acta Paediatr 1998;87:455–457.
- Pissard S, de Montalembert M, Bachir D, . Pyruvate kinase (PK) deficiency in newborns: the pitfalls of diagnosis. J Pediatr. 2007;150:443–445.
- Zanella A, Bianchi P. RBC pyruvate kinase deficiency: from genetics to clinical manifestations. Bailliere Clin Haematol. 2000;13:57–81.
- Agrawal SK, Kumar P, Rathi R, . UGT1A1 gene polymorphisms in North Indian neonates presenting with unconjugated hyperbilirubinemia. Pediatr Res. 2009;65:675–680.