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Journal Abstract Search

147 related items for PubMed ID: 19674361

  • 1. Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia.
    Boo NY, Wong FL, Wang MK, Othman A.
    Pediatr Int; 2009 Aug; 51(4):488-93. PubMed ID: 19674361
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  • 5. UGT1A1 gene mutations and neonatal hyperbilirubinemia in Guangxi Heiyi Zhuang and Han populations.
    Wu XJ, Zhong DN, Xie XZ, Ye DZ, Gao ZY.
    Pediatr Res; 2015 Nov; 78(5):585-8. PubMed ID: 26200705
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  • 6. Bilirubin Uridine Diphosphate-glucuronosyltransferase Polymorphism as a Risk Factor for Prolonged Hyperbilirubinemia in Japanese Preterm Infants.
    Yanagi T, Nakahara S, Maruo Y.
    J Pediatr; 2017 Nov; 190():159-162.e1. PubMed ID: 28888563
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  • 8. Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene.
    Maruo Y, Nishizawa K, Sato H, Sawa H, Shimada M.
    Pediatrics; 2000 Nov; 106(5):E59. PubMed ID: 11061796
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  • 9. Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong.
    Xu JX, Lin F, Chen ZK, Luo ZY, Zhan XF, Wu JR, Ma YB, Li JD, Yang LY.
    BMC Pediatr; 2021 Dec 11; 21(1):564. PubMed ID: 34895177
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  • 11. Neonatal hyperbilirubinemia and Gly71Arg mutation of UGT1A1 gene: a Chinese case-control study followed by systematic review of existing evidence.
    Long J, Zhang S, Fang X, Luo Y, Liu J.
    Acta Paediatr; 2011 Jul 11; 100(7):966-71. PubMed ID: 21272068
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  • 12. Variants of organic anion transporter polypeptide 2 gene are not risk factors associated with severe neonatal hyperbilirubinemia.
    Wong FL, Boo NY, Ainoon O, Wang MK.
    Malays J Pathol; 2009 Dec 11; 31(2):99-104. PubMed ID: 20514852
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  • 13. Effects of Gly71Arg mutation in UGT1A1 gene on neonatal hyperbilirubinemia: a systematic review and meta-analysis.
    Mehrad-Majd H, Haerian MS, Akhtari J, Ravanshad Y, Azarfar A, Mamouri G.
    J Matern Fetal Neonatal Med; 2019 May 11; 32(10):1575-1585. PubMed ID: 29179591
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  • 14. UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China.
    Yang H, Lin F, Chen ZK, Zhang L, Xu JX, Wu YH, Gu JY, Ma YB, Li JD, Yang LY.
    BMC Pediatr; 2021 Jun 01; 21(1):259. PubMed ID: 34074250
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  • 17. Rapid detection of the UGT1A1 single nucleotide polymorphism G211A using real-time PCR with Taqman minor groove binder probes.
    Wong FL, Wang MK, Boo NY, Hamidah NH, Ainoon BO.
    J Clin Lab Anal; 2007 Jun 01; 21(3):167-72. PubMed ID: 17506482
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  • 18. Association of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants.
    Zhou Y, Wang SN, Li H, Zha W, Wang X, Liu Y, Sun J, Peng Q, Li S, Chen Y, Jin L.
    PLoS One; 2014 Jun 01; 9(8):e104251. PubMed ID: 25102181
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