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Journal Abstract Search

171 related items for PubMed ID: 17426648

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  • 4. Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism.
    Kaplan M, Hammerman C, Rubaltelli FF, Vilei MT, Levy-Lahad E, Renbaum P, Vreman HJ, Stevenson DK, Muraca M.
    Hepatology; 2002 Apr; 35(4):905-11. PubMed ID: 11915038
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  • 7. 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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  • 9. Contribution of haemolysis to jaundice in Sephardic Jewish glucose-6-phosphate dehydrogenase deficient neonates.
    Kaplan M, Vreman HJ, Hammerman C, Leiter C, Abramov A, Stevenson DK.
    Br J Haematol; 1996 Jun; 93(4):822-7. PubMed ID: 8703811
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  • 11. Bilirubin conjugation, reflected by conjugated bilirubin fractions, in glucose-6-phosphate dehydrogenase-deficient neonates: a determining factor in the pathogenesis of hyperbilirubinemia.
    Kaplan M, Muraca M, Hammerman C, Vilei MT, Leiter C, Rudensky B, Rubaltelli FF.
    Pediatrics; 1998 Sep; 102(3):E37. PubMed ID: 9724685
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  • 12. (TA)n UDP-glucuronosyltransferase 1A1 promoter polymorphism in Nigerian neonates.
    Kaplan M, Slusher T, Renbaum P, Essiet DF, Pam S, Levy-Lahad E, Hammerman C.
    Pediatr Res; 2008 Jan; 63(1):109-11. PubMed ID: 18043502
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  • 13. A causal relationship between UDP-glucuronosyltransferase 1A1 promoter polymorphism and idiopathic hyperbilirubinemia in Turkish newborns.
    Ergin H, Bican M, Atalay OE.
    Turk J Pediatr; 2010 Jan; 52(1):28-34. PubMed ID: 20402064
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  • 15. [Roles of UGT 1A1 gene mutation in the development of neonatal hyperbilirubinemia in Guangxi].
    Gao ZY, Zhong DN, Liu Y, Liu YN, Wei LM.
    Zhonghua Er Ke Za Zhi; 2010 Sep; 48(9):646-9. PubMed ID: 21092520
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  • 19. [A study of polymorphism in UDP-glucuronosyltransferase 1 (UGT-1A1) promoter gene in Korean patients with Gilbert's syndrome].
    Kim YH, Yeon JE, Jung GM, Kim HJ, Kim JS, Byun KS, Bak YT, Lee CH.
    Taehan Kan Hakhoe Chi; 2002 Jun; 8(2):132-8. PubMed ID: 12499798
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