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Journal Abstract Search

180 related items for PubMed ID: 520367

  • 1.
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  • 2. 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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  • 3. Dubin-Johnson Syndrome. Abnormal excretion of the isomers of urinary coproporphyrin by clinically unaffected family members.
    Ben-Ezzer J, Blonder J, Shani M, Seligsohn U, Post CA, Adam A, Szeinberg A.
    Isr J Med Sci; 1973 Feb; 9(9):1431-6. PubMed ID: 4775130
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  • 5. Neonatal cholestasis in two siblings: a variant of Dubin-Johnson syndrome?
    Kimura A, Yuge K, Kosai KI, Kage M, Fujisawa T, Inoue T, Yamashita Y, Nakashima E, Kato H.
    J Paediatr Child Health; 1995 Dec; 31(6):557-60. PubMed ID: 8924312
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  • 9. Clinical expression of co-inherited Dubin-Johnson and thalassaemic heterozygous states.
    Fretzayas A, Kitsiou S, Papadopoulou A, Nicolaidou P.
    Dig Liver Dis; 2007 Apr; 39(4):369-74. PubMed ID: 16563888
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  • 10. 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
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  • 11. [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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  • 12. Urinary coproporphyrins as a diagnostic biomarker of Dubin-Johnson syndrome in neonates: A diagnostic pathway is proposed.
    Al-Hussaini A, Asery A, Alharbi O.
    Saudi J Gastroenterol; 2023 Sep; 29(3):183-190. PubMed ID: 37313948
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  • 16. Dubin-Johnson syndrome as a cause of neonatal jaundice: the importance of coproporphyrins investigation.
    Haimi-Cohen Y, Merlob P, Marcus-Eidlits T, Amir J.
    Clin Pediatr (Phila); 1998 Aug; 37(8):511-3. PubMed ID: 9729708
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  • 19. [Conjugated hyperbilirubinemia with pigment in the liver (Dubin-Johnson syndrome) in a newborn infant].
    Ivicic L, Sosovec V.
    Cesk Pediatr; 1975 Jun; 30(6):287-8. PubMed ID: 1157182
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  • 20. Uroporphyrinogen III cosynthetase in liver and blood in the Dubin-Johnson syndrome.
    Shimizu Y, Kondo T, Kuchiba K, Urata G.
    J Lab Clin Med; 1977 Mar; 89(3):517-23. PubMed ID: 839109
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