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Journal Abstract Search

184 related items for PubMed ID: 24232666

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. The relationship between hyperbilirubinemia and the promoter region and first exon of UGT1A1 gene polymorphisms in Vietnamese newborns.
    Nguyen TT, Zhao W, Yang X, Zhong DN.
    Pediatr Res; 2020 Dec; 88(6):940-944. PubMed ID: 32126570
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Effect of genetic variants of bilirubin metabolism on the degree of hyperbilirubinemia in African-American newborns.
    Schutzman DL, Baudhuin LM, Gatien E, Ajayi S, Wong RJ.
    J Perinatol; 2017 Apr; 37(4):432-435. PubMed ID: 27977017
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. UGT1A1 gene and neonatal hyperbilirubinemia: a preliminary study from Bengkulu, Indonesia.
    Amandito R, Putradista R, Jikesya C, Utaminingsih D, Rusin J, Rohsiswatmo R, Malik A.
    BMC Res Notes; 2018 Mar 13; 11(1):172. PubMed ID: 29534743
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  • 9. 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 13; 190():159-162.e1. PubMed ID: 28888563
    [Abstract] [Full Text] [Related]

  • 10. Genetic polymorphisms in Thai neonates with hyperbilirubinemia.
    Prachukthum S, Nunnarumit P, Pienvichit P, Chuansumrit A, Songdej D, Kajanachumpol S, Pakakasama S, Hongeng S.
    Acta Paediatr; 2009 Jul 13; 98(7):1106-10. PubMed ID: 19397531
    [Abstract] [Full Text] [Related]

  • 11. Developmental, Genetic, Dietary, and Xenobiotic Influences on Neonatal Hyperbilirubinemia.
    Yueh MF, Chen S, Nguyen N, Tukey RH.
    Mol Pharmacol; 2017 May 13; 91(5):545-553. PubMed ID: 28283555
    [Abstract] [Full Text] [Related]

  • 12. The role of UGT1A1 promoter polymorphism and exon-1 mutations in neonatal jaundice.
    Halis H, Ergin H, Köseler A, Atalay EÖ.
    J Matern Fetal Neonatal Med; 2017 Nov 13; 30(22):2658-2664. PubMed ID: 27842454
    [Abstract] [Full Text] [Related]

  • 13. Association between the Specific UGT1A1 Promoter Sequence Variant (c-3279T>G) and Unconjugated Neonatal Hyperbilirubinemia.
    Tomerak RH, Helal NF, Shaker OG, Yousef MA.
    J Trop Pediatr; 2016 Dec 13; 62(6):457-463. PubMed ID: 27318112
    [Abstract] [Full Text] [Related]

  • 14. [Study on spectrum of UGT1A1 mutations in connection with inherited non-hemolytic unconjugated hyperbilirubinemia].
    Xiong QF, Zhong YD, Feng XN, Zhou H, Liu DX, Wu XP, Yang YF.
    Zhonghua Gan Zang Bing Za Zhi; 2018 Dec 20; 26(12):898-902. PubMed ID: 30669781
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  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 72(2):169-73. PubMed ID: 22580719
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 57(4):310-7. PubMed ID: 26727668
    [Abstract] [Full Text] [Related]

  • 19. Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia.
    Boo NY, Wong FL, Wang MK, Othman A.
    Pediatr Int; 2009 Aug 01; 51(4):488-93. PubMed ID: 19674361
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 69(2):170-4. PubMed ID: 20975617
    [Abstract] [Full Text] [Related]

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