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Journal Abstract Search

181 related items for PubMed ID: 8596313

  • 41. FEATURES OF GILBERT'S SYNDROME IN PATIENTS WITH DIFFERENT GENOTYPES UGT1AI.
    Kurilovich SA, Nemtsova EG, Kruchinina MV, Maximov VN.
    Eksp Klin Gastroenterol; 2016; (9):32-37. PubMed ID: 29889392
    [Abstract] [Full Text] [Related]

  • 42. UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias.
    Khan S, Irfan M, Sher G, Zubaida B, Alvi MA, Yasinzai M, Naeem M.
    Ann Hum Genet; 2013 Nov; 77(6):482-7. PubMed ID: 23992562
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  • 43. Gilbert's syndrome is not associated with HELLP syndrome.
    Zusterzeel PL, te Morsche R, Raijmakers MT, Peters WH, Steegers EA.
    BJOG; 2001 Sep; 108(9):1003-4. PubMed ID: 11563452
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  • 44. Gilbert's syndrome--clinical and pharmacological implications.
    Radu P, Atsmon J.
    Isr Med Assoc J; 2001 Aug; 3(8):593-8. PubMed ID: 11519385
    [No Abstract] [Full Text] [Related]

  • 45. Inherited disorders of bilirubin clearance.
    Memon N, Weinberger BI, Hegyi T, Aleksunes LM.
    Pediatr Res; 2016 Mar; 79(3):378-86. PubMed ID: 26595536
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  • 48. Liver bilirubin UDP-glucuronosyltransferase activity in chronic nonhemolytic unconjugated hyperbilirubinemia of adults.
    Watanabe A, Wakabayashi H, Kuwabara Y, Yamamoto H, Hattori S, Tsuji T.
    Res Exp Med (Berl); 1998 Apr; 197(6):329-36. PubMed ID: 9638795
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  • 50. Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase.
    Koiwai O, Nishizawa M, Hasada K, Aono S, Adachi Y, Mamiya N, Sato H.
    Hum Mol Genet; 1995 Jul; 4(7):1183-6. PubMed ID: 8528206
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  • 51. [Molecular diagnosis of heritable unconjugated hyperbilirubinemias].
    Mammaev SN.
    Klin Lab Diagn; 2005 Dec; (12):8-13. PubMed ID: 16498946
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  • 55. [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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  • 56. Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome.
    Minucci A, Ruggiero A, Canu G, Maurizi P, De Bonis M, Concolino P, De Luca D, Capoluongo E.
    Pediatr Blood Cancer; 2015 Sep; 62(9):1680-1. PubMed ID: 25822733
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  • 57. Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type II.
    Iijima S, Ohzeki T, Maruo Y.
    Yonsei Med J; 2011 Mar; 52(2):369-72. PubMed ID: 21319362
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  • 58. Hepatic uptake of organic anions affects the plasma bilirubin level in subjects with Gilbert's syndrome mutations in UGT1A1.
    Persico M, Persico E, Bakker CT, Rigato I, Amoroso A, Torella R, Bosma PJ, Tiribelli C, Ostrow JD.
    Hepatology; 2001 Mar; 33(3):627-32. PubMed ID: 11230743
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  • 59. [Relationship between bilirubin UDP-glucuronosyl transferase polymorphism and neonatal jaundice].
    Sha B.
    Zhongguo Dang Dai Er Ke Za Zhi; 2007 Oct; 9(5):510-3. PubMed ID: 17937877
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  • 60. [Clinical and genetic analyses of UGT1A1 gene from a Chinese family with Gilbert's syndrome].
    Peng XX, Jiang J.
    Zhonghua Yi Xue Za Zhi; 2010 Jun 22; 90(24):1690-3. PubMed ID: 20979879
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