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Journal Abstract Search

163 related items for PubMed ID: 25102181

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  • 4. 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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  • 6. 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; 155(6):860-3. PubMed ID: 19683255
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  • 7. 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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  • 15. Association of polymorphisms in four bilirubin metabolism genes with serum bilirubin in three Asian populations.
    Lin R, Wang X, Wang Y, Zhang F, Wang Y, Fu W, Yu T, Li S, Xiong M, Huang W, Jin L.
    Hum Mutat; 2009 Apr; 30(4):609-15. PubMed ID: 19243019
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  • 17. Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population.
    Fan J, He HY, Li HH, Wu PL, Tang L, Deng BY, Dong WH, Wang JH.
    BMC Pediatr; 2024 Jan 26; 24(1):82. PubMed ID: 38279097
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  • 18. 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 26; 100(7):966-71. PubMed ID: 21272068
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