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Journal Abstract Search

169 related items for PubMed ID: 766621

  • 1. Rotor's syndrome. A distinct inheritable pathophysiologic entity.
    Wolkoff AW, Wolpert E, Pascasio FN, Arias IM.
    Am J Med; 1976 Feb; 60(2):173-9. PubMed ID: 766621
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  • 7. Abnormal sulfobromophthalein metabolism in Rotor's syndrome and obligate heterozygotes.
    Wolpert E, Pascasio FM, Wolkoff AW, Arias IM.
    N Engl J Med; 1977 May 12; 296(19):1099-101. PubMed ID: 850521
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  • 8. Porphyrins in Rotor's syndrome: a study on an Italian family.
    Rapaccini GL, Topi GC, Anti M, D'Alessandro Gandolfo L, Griso D, Amantea A, de Vitis I, Fedeli G.
    Hepatogastroenterology; 1986 Feb 12; 33(1):11-3. PubMed ID: 3957223
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  • 10. Dubin-Johnson syndrome in a neonate.
    Nakata F, Oyanagi K, Fujiwara M, Sogawa H, Minami R, Horino K, Nakao T, Kondo T.
    Eur J Pediatr; 1979 Feb 12; 132(4):299-301. PubMed ID: 520367
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  • 12. Diagnostic and pathogenetic implications of urinary coproporphyrin excretion in the Dubin-Johnson syndrome.
    Frank M, Doss M, de Carvalho DG.
    Hepatogastroenterology; 1990 Feb 12; 37(1):147-51. PubMed ID: 2312040
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  • 13. [Rotor's syndrome. Apropos of a case].
    Carre D, Civadier C, Foll Y, Talarmin B, Abgrall J.
    Ann Gastroenterol Hepatol (Paris); 1994 Feb 12; 30(6):255-9. PubMed ID: 7847786
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  • 15. Urinary coproporphyrin isomer distribution in the Dubin-Johnson syndrome.
    Koskelo P, Toivonen I, Adlercreutz H.
    Clin Chem; 1967 Nov 12; 13(11):1006-9. PubMed ID: 6054688
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  • 16. [Constitutional hyperbilirubinemia and mixed bilirubin. Clinical and functional study].
    Rapaccini GL, Anti M, Miggiano G, De Vitis I, De Simone F, Fedeli G.
    Minerva Med; 1980 Nov 10; 71(44):3221-8. PubMed ID: 7454089
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  • 17. Abnormal excretion of the isomers of urinary coproporphyrin by patients with Dubin-Johnson syndrome in Israel.
    Ben-Ezzer J, Rimington C, Shani M, Seligsohn U, Sheba C, Szeinberg A.
    Clin Sci; 1971 Jan 10; 40(1):17-30. PubMed ID: 5539298
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  • 18. 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 10; 22(4):422-5. PubMed ID: 21948575
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