References
- Maisels MJ. Jaundice. In : Avery GB, Fletcher MA, Mac- Donald MG, editors. Neonatology : pathophysiology and management of the newborn. 5th ed. Philadelphia : JB Lippincott Co, 1999:765-819
- Friedman L, Lewis PJ, Clifton P, Bulpitt CJ. Factors influencing the incidence of neonatal jaundice. Br Med J 1978;1: 1235-7 https://doi.org/10.1136/bmj.1.6122.1235
- Horiguchi T, Bauer C. Ethnic differences in neonatal jaundice : Comparison of Japanese and Caucasian newborn infants. Am J Obstet Gynecol 1975;121:71-4 https://doi.org/10.1016/0002-9378(75)90978-3
- Linn S, Schoenbaum SC, Monson RR, Rosner B, Stubblefield PG, Ryan KJ. Epidemiology of neonatal hyperbilirubinemia. Pediatrics 1985;75:770-4
- Brown WR, Boon WH. Ethic group differences in plasma bilirubin levels of full-term, healthy Singapore newborns. Pediatrics 1965;36:745-51
- Khoury MJ, Calle EE, Joesoef RM. Recurrence risk of neonatal hyperbilirubinemia in siblings. Am J Dis Child 1988; 142:1065-9
- Newman TB, Easterlin MJ, Goldman ES, Stevenson DK. Laboratory evaluation of jaundice in newborns. Am J Dis Child 1990;144:364-8 https://doi.org/10.1001/archpedi.1990.02150270114039
- Gale R, Seidman DS, Dollberg S, Stervenson DK. Epidemiology of neonatal jaundice in the Jerusalem population. J Pediatr Gastroenterol Nutr 1990;10:82-6 https://doi.org/10.1097/00005176-199001000-00016
- Nielsen HE, Haase P, Blaabjerg J, Stryhn H, Hilden J. Risk factors and sib correlation in physiological neonatal jaundice. Acta Paediatr Scand 1987;76:504-11 https://doi.org/10.1111/j.1651-2227.1987.tb10507.x
- Drew JH, Kitchen WH. Jaundice in infants of greek parentage : the unknown factor may be environmental. J Pediatr 1976;89:248-52 https://doi.org/10.1016/S0022-3476(76)80457-X
- Koiwai O, Nishizawa M, Hasada K, Aono S, Adachi Y, Mamiya N, et al. Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDPglucuronosyltransferase. Hum Mol Genet 1995;4:1183-6. https://doi.org/10.1093/hmg/4.7.1183
- Yamamoto K, Sato H, Fujiyama Y, Doida Y, Bamba T. Contribution of two missense mutations(G71R and Y486D) of the bilirubin UDP glucosyltransferase(UGT1A1) gene phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II. Biochim Biophys Acta 1998;1406:267-73 https://doi.org/10.1016/S0925-4439(98)00013-1
- Kadakol A, Ghosh SS, Sappal BS, Sharma G, Chowdhury NR. Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase(UGT1A1) causing Crigler- Najjar and Gilbert syndromes : correlation of genotype to phenotype. Hum Mutat 2000;16:297-306 https://doi.org/10.1002/1098-1004(200010)16:4<297::AID-HUMU2>3.0.CO;2-Z
- Burchell B, Hume R. Molecular genetic basis of Gilbert's syndrome. J Gastroenterol Hepatol 1999;14:960-6 https://doi.org/10.1046/j.1440-1746.1999.01984.x
- Beutler E, Gelbart T, Demina A. Racial variability in the UDP-glucuronosyl transferase 1(UGT1A1) promoter : A balanced polymorphism for regulation of bilirubin metabolism?Proc Natl Acad Sci USA 1998;95:8170-4
- Monaghan G, Ryan M, Seddon R, Hume R, Burchell B. Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome. Lancet 1996;347: 578-81 https://doi.org/10.1016/S0140-6736(96)91273-8
- Ando Y, Chida M, Nakayama K, Saka H, Kamataki T. The UGT1A1*28 allele is relatively rare in a Japanese population. Pharmacogenetics 1998;8:357-60 https://doi.org/10.1097/00008571-199808000-00010
- Hong KW, Kang H, Kim IS, Kim JS, Kim ER, Lee HJ, et al. Polymorphism of UDP-glucuronosyltransferase gene (UGT1A1) of neonatal hyperbilirubinemia in Korea. Korean J Pediatr 2004;47:18-23
- Maruo Y, Nishizawa K, Sato H, Doida Y, Shimada M. Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism. Pediatrics 1999; 103:1224-7 https://doi.org/10.1542/peds.103.6.1224
- Huang CS, Chang PF, Huang MJ, Chen ES, Hung KL, Tsou KI. Relationship between bilirubin UDP-glucuronosyltransferase 1A1 gene and neonatal hyperbilirubinemia. Pediatr Res 2002;52:601-5 https://doi.org/10.1203/00006450-200210000-00022
- Yamamoto A, Nishio H, Waku S, Yokoyama N, Yonetani M, Uetani Y, et al. Gly71Arg mutation of the bilirubin UDP-glucuronosyltransferase 1A1 gene is associated with neonatal hyperbilirubinemia in the Japanese population. Kobe J Med Sci 2002;48:73-7.
- Akaba K, Kimura T, Sasaki A, Tanabe S, Ikegami T, Hashimoto M, et al. Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate glucuronosyltransferase gene : A common missense mutation among Japanese, Koreans and Chinese. Biochem Molec Biol Int 1998; 46:21-6
- Akaba K, Kimura T, Sasaki A, Tanabe S, Wakabayashi T, Hiroi M, et al. Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese. J Hum Genet 1999;44:22-5 https://doi.org/10.1007/s100380050100
- Kang H, Lim JH, Kim JS, Kim ER, Kim SD, Lee HJ, et al. The association of neonatal hyperbilirubinemia with UGT1A1 and CYP1A2 gene polymorphism in Korean neonate.Korean J Pediatr 2005;48:35-41
- Huang CS, Luo GA, Huang MJ, Yu SC, Yang SS. Variations of the bilirubin uridine-diphosphoglucuronosyl transferase 1A1 gene in healthy Taiwanese. Pharmacogenetics 2000;10:539-44 https://doi.org/10.1097/00008571-200008000-00007
- Maruo Y, Addario CD, Mori A, Iwai M, Takahashi H, Sato H, et al. Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome. Hum Genet 2004;115:525-6 https://doi.org/10.1007/s00439-004-1183-x
- Kanai M, Kijima K, Shirahata E, Sasaki A, Akaba K, Umetsu K, et al. Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate glucuronosyltransferase gene : the common -3263T> G mutation of phenobabital response enhancer module is not associated with the neoanatal hyperbilibinemia in Japanese. Pediatr Int 2005;47:137-41 https://doi.org/10.1111/j.1442-200x.2005.02030.x
- Ritter JK, Crawford JM, Owens IS. Cloning of two human liver bilirubin UDP-glucuronosyltransferase cDNAs with expression in COS-1 cells. J Biol Chem 1991;266:1043-7
- Bosma PJ, Chowdhury JR, Bakker C, Gantla S, de Boer A, Oostra BA, et al. The genetic basis of the reduced expression of bilirubin UDP-glucuronyltransferase 1 in Gilbert's syndrome. N Engl J Med 1995;333:1171-5 https://doi.org/10.1056/NEJM199511023331802
- Raijmarkers MT, Jansen PL, Steegers EA, Peters WH. Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promoter region of the UGT1A1 gene. J Hepatol 2000;33:348-51 https://doi.org/10.1016/S0168-8278(00)80268-8
- Takeuchi K, Kobayashi Y, Tamaki S, Maruo Y, Araki J, Mifuji R, et al. Genetic polymorphisms of bilirubin uridine diphosphate glucrononsyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects. J Gstroenterol Hepatol 2004;19:955-7 https://doi.org/10.1111/j.1440-1746.2004.03524.x
- Huang CS, Chang PF, Huang MJ, Chen ES, Chen WC. Glucose-6-phosphate dehydrogenase deficiency, the UDPglucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia. Gastroenterology 2002;123:127-33 https://doi.org/10.1053/gast.2002.34173
- Kim YH, Yeon JE, Jung GM, Kim HJ, Kim JS, Byun KS, et al. A study of polymorphism in UDP-glucuronyltransferase 1(UGT-1A1) promoter gene in Korean patients with Gilbert's syndrome. Korean J Hepatol 2002;8:132-8
- Bancroft JD, Kreamer B, Gourley GR. Gilbert,s syndrome accelerates development of neonatal jaundice. J Pediatr 1998;132:656-60 https://doi.org/10.1016/S0022-3476(98)70356-7
- Huang MJ, Kug KE, Teng Hc, Tang KS, Weng HW, Hung CS. Risk factors for severe hyperbilirubinemia in neonates. Pediatr Res 2004;56:682-9 https://doi.org/10.1203/01.PDR.0000141846.37253.AF
- Sutomo R, Talib NA, Yusoff NM, Van Rostenberghe H, Sadewa AH, Sunarti, et al. Screening for G71R mutation of the UGT1A1 gene in the Javanese- Indonesian and Malay- Malaysian populations. Pediatr Int 2004;46:565-9 https://doi.org/10.1111/j.1442-200x.2004.01959.x
- Sugatani J, Yamakawa K, Yoshinari K, Machida T, Takagi H, Mori M, et al. Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia. Biochem Biophys Res Commun 2002;292:492-7 https://doi.org/10.1006/bbrc.2002.6683