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Journal Abstract Search

96 related items for PubMed ID: 8592567

  • 1. The genetic basis of Gilbert's syndrome.
    Mathew P.
    N Engl J Med; 1996 Mar 21; 334(12):802-3. PubMed ID: 8592567
    [No Abstract] [Full Text] [Related]

  • 2. TATA-box mutant in the promoter of the uridine diphosphate glucuronosyltransferase gene in Italian patients with Gilbert's syndrome.
    Sampietro M, Lupica L, Perrero L, Romano R, Molteni V, Fiorelli G.
    Ital J Gastroenterol Hepatol; 1998 Apr 21; 30(2):194-8. PubMed ID: 9675658
    [Abstract] [Full Text] [Related]

  • 3. Gilbert's syndrome--a legitimate genetic anomaly?
    Schmid R.
    N Engl J Med; 1995 Nov 02; 333(18):1217-8. PubMed ID: 7565981
    [No Abstract] [Full Text] [Related]

  • 4. Correlation of mutational analysis to clinical features in Taiwanese patients with Gilbert's syndrome.
    Hsieh SY, Wu YH, Lin DY, Chu CM, Wu M, Liaw YF.
    Am J Gastroenterol; 2001 Apr 02; 96(4):1188-93. PubMed ID: 11316168
    [Abstract] [Full Text] [Related]

  • 5. The genetic basis of Gilbert's syndrome.
    Sato H, Adachi Y, Koiwai O.
    Lancet; 1996 Mar 02; 347(9001):557-8. PubMed ID: 8596313
    [No Abstract] [Full Text] [Related]

  • 6. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.
    Bosma PJ, Chowdhury JR, Bakker C, Gantla S, de Boer A, Oostra BA, Lindhout D, Tytgat GN, Jansen PL, Oude Elferink RP.
    N Engl J Med; 1995 Nov 02; 333(18):1171-5. PubMed ID: 7565971
    [Abstract] [Full Text] [Related]

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  • 9. Dual polymorphisms in UDP-glucuronosyltransferases 1A1 and 1A6: a novel mechanism for hyperserotoninaemia in Gilbert's syndrome mimicking carcinoid syndrome?
    Lee P, Jones G, Seibel MJ.
    Eur J Gastroenterol Hepatol; 2007 Apr 02; 19(4):337-40. PubMed ID: 17353700
    [Abstract] [Full Text] [Related]

  • 10. [From gene to disease; unconjugated hyperbilirubinemia: Gilbert's syndrome and Crigler-Najjar types I and II].
    Drenth JP, Peters WH, Jansen JB.
    Ned Tijdschr Geneeskd; 2002 Aug 10; 146(32):1488-90. PubMed ID: 12198827
    [Abstract] [Full Text] [Related]

  • 11. What is Gilbert's syndrome? Lesson from genetic polymorphisms of UGT1A1 in Gilbert's syndrome from Asia.
    Kamisako T.
    J Gastroenterol Hepatol; 2004 Sep 10; 19(9):955-7. PubMed ID: 15304109
    [No Abstract] [Full Text] [Related]

  • 12. [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 10; 8(2):132-8. PubMed ID: 12499798
    [Abstract] [Full Text] [Related]

  • 13. Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome.
    Iolascon A, Faienza MF, Giordani L, Perrotta S, Ruggiu G, Meloni GF, del Giudice EM.
    Eur J Haematol; 1999 May 10; 62(5):307-10. PubMed ID: 10359058
    [Abstract] [Full Text] [Related]

  • 14. Drug-mediated toxicity caused by genetic deficiency of UDP-glucuronosyltransferases.
    Burchell B, Soars M, Monaghan G, Cassidy A, Smith D, Ethell B.
    Toxicol Lett; 2000 Mar 15; 112-113():333-40. PubMed ID: 10720749
    [Abstract] [Full Text] [Related]

  • 15. Frequent co-occurrence of the TATA box mutation associated with Gilbert's syndrome (UGT1A1*28) with other polymorphisms of the UDP-glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and Egyptians.
    Köhle C, Möhrle B, Münzel PA, Schwab M, Wernet D, Badary OA, Bock KW.
    Biochem Pharmacol; 2003 May 01; 65(9):1521-7. PubMed ID: 12732365
    [Abstract] [Full Text] [Related]

  • 16. Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemia.
    Galanello R, Piras S, Barella S, Leoni GB, Cipollina MD, Perseu L, Cao A.
    Br J Haematol; 2001 Dec 01; 115(4):926-8. PubMed ID: 11843828
    [Abstract] [Full Text] [Related]

  • 17. Correlation of UGT1A1 TATA-box polymorphism and jaundice in breastfed newborns-early presentation of Gilbert's syndrome.
    Žaja O, Tiljak MK, Štefanović M, Tumbri J, Jurčić Z.
    J Matern Fetal Neonatal Med; 2014 May 01; 27(8):844-50. PubMed ID: 23981182
    [Abstract] [Full Text] [Related]

  • 18. Gilbert's syndrome is not associated with HELLP syndrome.
    Zusterzeel PL, te Morsche R, Raijmakers MT, Peters WH, Steegers EA.
    BJOG; 2001 Sep 01; 108(9):1003-4. PubMed ID: 11563452
    [Abstract] [Full Text] [Related]

  • 19. The combination of new missense mutation with [A(TA)7TAA] dinucleotide repeat in UGT1A1 gene promoter causes Gilbert's syndrome.
    D'Angelo R, Rinaldi C, Donato L, Nicocia G, Sidoti A.
    Ann Clin Lab Sci; 2015 Sep 01; 45(2):202-5. PubMed ID: 25887876
    [Abstract] [Full Text] [Related]

  • 20. Polymorphism in the promoter region of the bilirubin UDP-glucuronosyltransferase (Gilbert's syndrome) in healthy Dutch subjects.
    Te Morsche RH, Zusterzeel PL, Raijmakers MT, Roes EM, Steegers EA, Peters WH.
    Hepatology; 2001 Mar 01; 33(3):765. PubMed ID: 11230763
    [No Abstract] [Full Text] [Related]

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