Nkhoma ET, Poole C, Vannappagari V, Hall SA, Beutler E. The global prevalence of glucose-6-phosphate dehydrogenase deficiency: a systematic review and meta-analysis. Blood Cells Mol Dis 2009;42:267-78.
Cappellini MD, Fiorelli G. Glucose-6-phosphate dehydrogenase deficiency. Lancet 2008;371:64-74.
Simoons FJ. Plants of Life, plants of death. Madison: The University of Wisconsin Press, 1998.
Alving AS, Carson PE, Flanagan CL, Ickes CE. Enzymatic deficiency in primaquine-sensitive erythrocytes. Science 1956;124:484-5.
Mehta A, Mason PJ, Vulliamy TJ. Glucose-6-phosphate dehydrogenase deficiency. Baillieres Best Pract Res Clin Haematol 2000;13:21-38.
Allison AC. Glucose-6-phosphate dehydrogenase deficiency in red blood cells of East Africans. Nature 1960;186:531-2.
Bienzle U, Ayeni O, Lucas AO, Luzzatto L. Glucose-6-phosphate dehydrogenase and malaria. Greater resistance of females heterozygous for enzyme deficiency and of males with non-deficient variant. Lancet 1972;1:107-10.
Guindo A, Fairhurst RM, Doumbo OK, Wellems TE, Diallo DA. X-linked G6PD deficiency protects hemizygous males but not heterozygous females against severe malaria. PLoS Med 2007;4:e66.
Ruwende C, Khoo SC, Snow RW, et al. Natural selection of hemi- and heterozygotes for G6PD deficiency in Africa by resistance to severe malaria. Nature 1995;376:246-9.
Roth EF Jr, Raventos-Suarez C, Rinaldi A, Nagel RL. Glucose-6-phosphate dehydrogenase deficiency inhibits in vitro growth of Plasmodium falciparum. Proc Natl Acad Sci U S A 1983;80:298-9.
Luzzatto L, Usanga FA, Reddy S. Glucose-6-phosphate dehydrogenase deficient red cells: resistance to infection by malarial parasites. Science 1969;164:839-42.
Naylor CE, Rowland P, Basak AK, et al. Glucose 6-phosphate dehydrogenase mutations causing enzyme deficiency in a model of the tertiary structure of the human enzyme. Blood 1996;87:2974-82.
Marks PA, Johnson AB. Relationship between the age of human erythrocytes and their osmotic resistance: a basis for separating young and old erythrocytes. J Clin Invest 1958;37:1542-8.
Minucci A, Moradkhani K, Hwang MJ, Zuppi C, Giardina B, Capoluongo E. Glucose-6-phosphate dehydrogenase (G6PD) mutations database: review of the "old" and update of the new mutations. Blood Cells Mol Dis 2012;48:154-65.
Lee GB, Lee SJ, Kim YJ, et al. A case of G-6-PD Guadalajara. Korean J Pediatr 2004;47:210-3.
Kim KM, Lee JH, Chun CS. Jaundice and hemolytic anemia appearing within the first 24 hour of life due to glucose-6-phosphate dehydrogenase deficiency. Korean J Perinatol 2006;17:89-93.
Park SW, Lee HJ, Lee W, Whang KT. A case of glucose-6phosphate dehydrogenase riley causing hemolytic anemia. Korean J Hematol 1999;34:334-7.
Blackwell RQ, Ro IH, Yen L. Low incidence of erythrocyte G-6-PD deficiency in Koreans. Vox Sang 1968;14:299-303.
Beutler E. Red cell metabolism: a manual of biochemical methods. 3rd ed. New York: Grune & Stratton, 1984.
Beutler E. A series of new screening procedures for pyruvate kinase deficiency, glucose-6-phosphate dehydrogenase deficiency, and glutathione reductase deficiency. Blood 1966;28:553-62.
Tantular IS, Kawamoto F. An improved, simple screening method for detection of glucose-6-phosphate dehydrogenase deficiency. Trop Med Int Health 2003;8:569-74.
Jalloh A, Tantular IS, Pusarawati S, et al. Rapid epidemiologic assessment of glucose-6-phosphate dehydrogenase deficiency in malaria-endemic areas in Southeast Asia using a novel diagnostic kit. Trop Med Int Health 2004;9:615-23.
Ko DH, Jun SH, Park KU, Song SH, Kim JQ, Song J. Newborn screening for galactosemia by a second-tier multiplex enzyme assay using UPLC-MS/MS in dried blood spots. J Inherit Metab Dis 2011;34:409-14.
Ko DH, Jun SH, Park HD, et al. Multiplex enzyme assay for galactosemia using ultraperformance liquid chromatography-tandem mass spectrometry. Clin Chem 2010;56:764-71.
Song J. RBC enzyme analysis. Clin Pediatr Hematol Oncol 2013;20:8-12.
Ringelhahn B. A simple laboratory procedure for the recognition of A - (African type) G-6PD deficiency in acute haemolytic crisis. Clin Chim Acta 1972;36:272-4.
Glucose-6-phosphate dehydrogenase deficiency. WHO Working Group. Bull World Health Organ 1989;67:601-11.
The Korean Society of Hematology. Hematology. 2nd ed. Seoul: E-public, 2011.
Orkin SH, Nathan DG, Ginsburg D, Look AT, Fisher DE, Lux S IV. Nathan and Oski's hematology of infancy and childhood. 7th ed. Philadelphia: Saunders, 2008.
Dern RJ, McCurdy PR, Yoshida A. A new structural variant of glucose-6-phosphate dehydrogenase with a high production rate (G6PD Hektoen). J Lab Clin Med 1969;73:283-90.
McCaffrey RP, Halsted CH, Wahab MF, Robertson RP. Chloramphenicol-induced hemolysis in Caucasian glucose-6phosphate dehydrogenase deficiency. Ann Intern Med 1971;74:722-6.
Tugwell P. Glucose-6-phosphate-dehydrogenase deficiency in Nigerians with jaundice associated with lobar pneumonia. Lancet 1973;1:968-9.
Siddiqui T, Khan AH. Hepatitis A and cytomegalovirus infection precipitating acute hemolysis in glucose-6-phosphate dehydrogenase deficiency. Mil Med 1998;163:434-5.
Johnson LH, Bhutani VK, Brown AK. System-based approach to management of neonatal jaundice and prevention of kernicterus. J Pediatr 2002;140:396-403.
Nair PA, Al Khusaiby SM. Kernicterus and G6PD deficiency--a case series from Oman. J Trop Pediatr 2003;49:74-7.
American Academy of Pediatrics Subcommittee on Hyperbilirubinemia. Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation. Pediatrics 2004;114:297-316.
Kaplan M, Vreman HJ, Hammerman C, Leiter C, Abramov A, Stevenson DK. Contribution of haemolysis to jaundice in Sephardic Jewish glucose-6-phosphate dehydrogenase deficient neonates. Br J Haematol 1996;93:822-7.
Fiorelli G, Martinez di Montemuros F, Cappellini MD. Chronic non-spherocytic haemolytic disorders associated with glucose-6-phosphate dehydrogenase variants. Baillieres Best Pract Res Clin Haematol 2000;13:39-55.
Brian MC, Carbon PP. Current therapy in hematology-oncology, 1985-1986. Saint Louis: C.V. Mosby Co, 1985.
Beutler E, Kuhl W, Fox M, Tabsh K, Crandall BF. Prenatal diagnosis of glucose-6-phosphate-dehydrogenase deficiency. Acta haematol 1992;87:103-4.
Ahn HS. Textbook of pediatrics, 10th ed. Seoul: Mirae N Co, 2012:325.
Beutler E, Mathai CK, Smith JE. Biochemical variants of glucose-6-phosphate dehydrogenase giving rise to congenital nonspherocytic hemolytic disease. Blood 1968;31:131-50.
Hamilton JW, Jones FG, McMullin MF. Glucose-6-phosphate dehydrogenase Guadalajara--a case of chronic non-spherocytic haemolytic anaemia responding to splenectomy and the role of splenectomy in this disorder. Hematology 2004;9:307-9.