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Journal Abstract Search

215 related items for PubMed ID: 15864125

  • 1.
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  • 2. Molecular genetics of unconjugated hyperbilirubinemia in Taiwanese.
    Huang CS.
    J Biomed Sci; 2005; 12(3):445-50. PubMed ID: 15965581
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  • 4. Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia.
    Huang CS, Chang PF, Huang MJ, Chen ES, Chen WC.
    Gastroenterology; 2002 Jul; 123(1):127-33. PubMed ID: 12105841
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  • 6. Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonates.
    D'Silva S, Colah RB, Ghosh K, Mukherjee MB.
    Gene; 2014 Aug 15; 547(1):18-22. PubMed ID: 24865931
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  • 7. Contribution of UGT1A1 variations to chemotherapy-induced unconjugated hyperbilirubinemia in pediatric leukemia patients.
    Nomura A, Maruo Y, Taga T, Takeuchi Y.
    Pediatr Res; 2016 Aug 15; 80(2):252-7. PubMed ID: 27057738
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  • 8. Risk factors associated with unconjugated neonatal hyperbilirubinemia in Malaysian neonates.
    Wong F, Boo N, Othman A.
    J Trop Pediatr; 2013 Aug 15; 59(4):280-5. PubMed ID: 23640907
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  • 10. 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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  • 12. 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
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  • 16. Identification of Promotor and Exonic Variations, and Functional Characterization of a Splice Site Mutation in Indian Patients with Unconjugated Hyperbilirubinemia.
    Gupta N, Benjamin M, Kar A, Munjal SD, Sarangi AN, Dalal A, Aggarwal R.
    PLoS One; 2015 Aug 01; 10(12):e0145967. PubMed ID: 26716871
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  • 20. Effects of variant UDP-glucuronosyltransferase 1A1 gene, glucose-6-phosphate dehydrogenase deficiency and thalassemia on cholelithiasis.
    Huang YY, Huang CS, Yang SS, Lin MS, Huang MJ, Huang CS.
    World J Gastroenterol; 2005 Sep 28; 11(36):5710-3. PubMed ID: 16237771
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