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Journal Abstract Search

131 related items for PubMed ID: 5539298

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  • 4. Relevance of urinary coproporphyrin isomers in hereditary hyperbilirubinemias.
    Frank M, Doss MO.
    Clin Biochem; 1989 Jun; 22(3):221-2. PubMed ID: 2736773
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  • 8. BENIGN JAUNDICE: THE DUBIN-JOHNSON AND ROTOR SYNDROMES.
    POLAND MD, PICKETT RD, ROSENAK BD.
    J Indiana State Med Assoc; 1965 May; 58():429-34. PubMed ID: 14289385
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  • 13. Diagnostic and pathogenetic implications of urinary coproporphyrin excretion in the Dubin-Johnson syndrome.
    Frank M, Doss M, de Carvalho DG.
    Hepatogastroenterology; 1990 Feb; 37(1):147-51. PubMed ID: 2312040
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  • 14. Severe jaundice due to coexistence of Dubin-Johnson syndrome and hereditary spherocytosis: a case report.
    Korkmaz U, Duman AE, Oğütmen Koç D, Gürbüz Y, Dındar G, Ensaroğlu F, Sener SY, Sentürk O, Hülagü S.
    Turk J Gastroenterol; 2011 Aug; 22(4):422-5. PubMed ID: 21948575
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  • 16. Porphobilinogen deaminase and the synthesis of porphyrin isomers in the Dubin-Johnson syndrome.
    Cohen C, Kirsch RE, Moore MR.
    S Afr Med J; 1986 Jul 05; 70(1):36-9. PubMed ID: 3726684
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  • 18. [Rotor syndrome: relevance of the determination of coproporphyrin isomers in the urine in comparison with intrahepatic (alcohol-induced) cholestasis].
    Both P, Frank M, Merkel HG, Doss M.
    Z Gastroenterol; 1988 Aug 05; 26(8):416-20. PubMed ID: 3218284
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  • 19. Inheritance of the Dubin-Johnson syndrome.
    Wolkoff AW, Cohen LE, Arias IM.
    N Engl J Med; 1973 Jan 18; 288(3):113-7. PubMed ID: 4682034
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  • 20. The inheritance of Dubin-Johnson syndrome.
    Shani M, Seligsohn U, Adam A.
    Isr J Med Sci; 1973 Jan 18; 9(9):1427-30. PubMed ID: 4775129
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