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Journal Abstract Search

440 related items for PubMed ID: 18460254

  • 21. Inheritance of the Dubin-Johnson-Sprinz syndrome.
    Edwards RH.
    Gastroenterology; 1975 Apr; 68(4 Pt 1):734-49. PubMed ID: 1123140
    [No Abstract] [Full Text] [Related]

  • 22. Familial nonhemolytic jaundice with free and conjugated hyperbilirubinemia, elevated serum bile acids, and liver pigmentation.
    Mihas AA, Kirby JD, Hirschowitz BI.
    South Med J; 1979 Aug; 72(8):1014-6. PubMed ID: 472798
    [Abstract] [Full Text] [Related]

  • 23. Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2.
    Slachtova L, Seda O, Behunova J, Mistrik M, Martasek P.
    Eur J Hum Genet; 2016 May; 24(5):704-9. PubMed ID: 26350512
    [Abstract] [Full Text] [Related]

  • 24. Treatment of severe cholestasis in neonatal Dubin-Johnson syndrome with ursodeoxycholic acid.
    Regev RH, Stolar O, Raz A, Dolfin T.
    J Perinat Med; 2002 May; 30(2):185-7. PubMed ID: 12012642
    [Abstract] [Full Text] [Related]

  • 25. A new mutation of the ATP-binding cassette, sub-family C, member 2 (ABCC2) gene in a Japanese patient with Dubin-Johnson syndrome.
    Tate G, Li M, Suzuki T, Mitsuya T.
    Genes Genet Syst; 2002 Apr; 77(2):117-21. PubMed ID: 12087194
    [Abstract] [Full Text] [Related]

  • 26. Gene replacement therapy for genetic hepatocellular jaundice.
    van Dijk R, Beuers U, Bosma PJ.
    Clin Rev Allergy Immunol; 2015 Jun; 48(2-3):243-53. PubMed ID: 25315738
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  • 28. [Familial benign conjugated hyperbilirubinemia with the presence of a pigment in the liver (Dubin-Johnson syndrome). Description of 3 cases in siblings].
    Sosovec V, Pesek J.
    Vnitr Lek; 1971 Apr; 17(4):382-7. PubMed ID: 5581194
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  • 30. [The Dubin-Johnson syndrome: case report and review of literature].
    Bosia JD, D'Ascenzo MV, Borzi S, Cozzi S, Defelitto JR, Curciarello JO.
    Acta Gastroenterol Latinoam; 2008 Sep; 38(3):194-8. PubMed ID: 18979899
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  • 32. Neonatal Dubin-Johnson syndrome: novel compound heterozygous mutation in the ABCC2 gene.
    Okada H, Kusaka T, Fuke N, Kunikata J, Kondo S, Iwase T, Nan W, Hirota T, Ieiri I, Itoh S.
    Pediatr Int; 2014 Oct; 56(5):e62-4. PubMed ID: 25336012
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  • 35. Dubin-Johnson and Rotor syndromes: molecular basis and pathogenesis.
    Zimniak P.
    Semin Liver Dis; 1993 Aug; 13(3):248-60. PubMed ID: 8235715
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  • 37. Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome.
    Kartenbeck J, Leuschner U, Mayer R, Keppler D.
    Hepatology; 1996 May; 23(5):1061-6. PubMed ID: 8621134
    [Abstract] [Full Text] [Related]

  • 38. Dubin-Johnson syndrome with systemic lupus erythematosus: a case report.
    Mahtab MA, Karim MF, Rahman S, Adnan AB.
    Hepatobiliary Pancreat Dis Int; 2006 Nov; 5(4):617-9. PubMed ID: 17085354
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  • 40. Identification of a novel 974C-->G nonsense mutation of the MRP2/ABCC2 gene in a patient with Dubin-Johnson syndrome and analysis of the effects of rifampicin and ursodeoxycholic acid on serum bilirubin and bile acids.
    Corpechot C, Ping C, Wendum D, Matsuda F, Barbu V, Poupon R.
    Am J Gastroenterol; 2006 Oct; 101(10):2427-32. PubMed ID: 16952291
    [Abstract] [Full Text] [Related]

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