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157 related items for PubMed ID: 29179591

  • 1. 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; 32(10):1575-1585. PubMed ID: 29179591
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  • 5. Association of Neonatal Hyperbilirubinemia with UGT1A1 Gene Polymorphisms: A Meta-Analysis.
    Yu Z, Zhu K, Wang L, Liu Y, Sun J.
    Med Sci Monit; 2015 Oct 15; 21():3104-14. PubMed ID: 26467199
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  • 8. Association between UGT 1A1 Gly71Arg (G71R) polymorphism and neonatal hyperbilirubinemia.
    Prachukthum S, Gamnarai P, Kangsadalampai S.
    J Med Assoc Thai; 2012 Jan 15; 95 Suppl 1():S13-7. PubMed ID: 23964438
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  • 10. 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 15; 78(5):585-8. PubMed ID: 26200705
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  • 11. 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 Nov 15; 9(8):e104251. PubMed ID: 25102181
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  • 12. Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia.
    Boo NY, Wong FL, Wang MK, Othman A.
    Pediatr Int; 2009 Aug 15; 51(4):488-93. PubMed ID: 19674361
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  • 15. UGT1A1*28 gene polymorphism was not associated with the risk of neonatal hyperbilirubinemia: a meta-analysis.
    Li H, Zhang P.
    J Matern Fetal Neonatal Med; 2021 Dec 15; 34(24):4064-4071. PubMed ID: 31818155
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  • 17. Prolonged unconjugated hyperbiliriubinemia in breast-fed male infants with a mutation of uridine diphosphate-glucuronosyl transferase.
    Chang PF, Lin YC, Liu K, Yeh SJ, Ni YH.
    J Pediatr; 2009 Dec 15; 155(6):860-3. PubMed ID: 19683255
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  • 19. 211 G to a variation of UDP-glucuronosyl transferase 1A1 gene and neonatal breastfeeding jaundice.
    Chou HC, Chen MH, Yang HI, Su YN, Hsieh WS, Chen CY, Chen HL, Chang MH, Tsao PN.
    Pediatr Res; 2011 Feb 15; 69(2):170-4. PubMed ID: 20975617
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  • 20. Clinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia.
    Yang H, Wang Q, Zheng L, Zheng XB, Lin M, Zhan XF, Yang LY.
    Pediatr Neonatol; 2016 Aug 15; 57(4):310-7. PubMed ID: 26727668
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