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Journal Abstract Search

189 related items for PubMed ID: 33158427

  • 21. Heme oxygenase-1 gene variants and hyperbilirubinemia risk in North Indian newborns.
    Tiwari PK, Sethi A, Basu S, Raman R, Kumar A.
    Eur J Pediatr; 2013 Dec; 172(12):1627-32. PubMed ID: 23877636
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  • 26. UGT1A1 gene polymorphisms in North Indian neonates presenting with unconjugated hyperbilirubinemia.
    Agrawal SK, Kumar P, Rathi R, Sharma N, DAS R, Prasad R, Narang A.
    Pediatr Res; 2009 Jun; 65(6):675-80. PubMed ID: 19430380
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  • 27. UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association?
    Alencastro de Azevedo L, Reverbel da Silveira T, Carvalho CG, Martins de Castro S, Giugliani R, Matte U.
    Pediatr Res; 2012 Aug; 72(2):169-73. PubMed ID: 22580719
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  • 30. Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients.
    Narter F, Can G, Ergen A, Isbir T, Ince Z, Çoban A.
    J Matern Fetal Neonatal Med; 2011 Feb; 24(2):313-6. PubMed ID: 20528217
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  • 36. UGT1A1 variants in Chinese Uighur and Han newborns and its correlation with neonatal hyperbilirubinemia.
    Yang H, Li H, Xia Q, Dai W, Li X, Liu Y, Nie J, Yang F, Sun Y, Feng L, Yang L.
    PLoS One; 2022 Feb; 17(12):e0279059. PubMed ID: 36520959
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  • 37. [Correlation between polymorphism in the promoter of DNA methyltransferase-3B and the risk of colorectal cancer].
    Bao Q, He BS, Chen LP, Gu L, Nie ZL, Wang SK.
    Zhonghua Yu Fang Yi Xue Za Zhi; 2012 Jan; 46(1):53-7. PubMed ID: 22490141
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  • 38. UGT1A1 gene variants and clinical risk factors modulate hyperbilirubinemia risk in newborns.
    Tiwari PK, Bhutada A, Agarwal R, Basu S, Raman R, Kumar A.
    J Perinatol; 2014 Feb; 34(2):120-4. PubMed ID: 24232666
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  • 39. Genetic Factors and Delayed TSB Monitoring and Treatment as Risk Factors Associated with Severe Hyperbilirubinemia in Term Neonates Admitted for Phototherapy.
    Boo NY, Sin S, Chee SC, Mohamed M, Ahluwalia AK, Ling MM, Ong HK.
    J Trop Pediatr; 2020 Dec 01; 66(6):569-582. PubMed ID: 32577754
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  • 40. 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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