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Journal Abstract Search

152 related items for PubMed ID: 5729564

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  • 2. Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency. Clinical, biochemical, pharmacologic and genetic evidence for heterogeneity.
    Arias IM, Gartner LM, Cohen M, Ezzer JB, Levi AJ.
    Am J Med; 1969 Sep; 47(3):395-409. PubMed ID: 4897277
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  • 4. [Crigler-Naijar syndrome. Clinical, biochemical, morphologic and therapeutic aspects].
    Götze H, Sidiropoulos D, Hess FA, Berthelot P.
    Helv Paediatr Acta; 1972 Jul; 27(3):335-51. PubMed ID: 4645658
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  • 5. 'In vitro' assay of bilirubin-UDP glucuronyl transferase activity in the liver of patients with Gilbert's syndrome and a variety of hepatic disorders.
    Black M, Billing BH.
    Gut; 1968 Dec; 9(6):728-9. PubMed ID: 5717986
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  • 7. Hepatic bilirubin glucuronidation in Gilbert's syndrome.
    Felsher BF, Craig JR, Carpio N.
    J Lab Clin Med; 1973 Jun; 81(6):829-37. PubMed ID: 4710368
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  • 12. Therapy in congenital hyperbilirubinemia: phenobarbital and diethylnicotinamide.
    Ertel IJ, Newton WA.
    Pediatrics; 1969 Jul; 44(1):43-8. PubMed ID: 5795402
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  • 14. [Phenobarbital therapy in congenital nonhemolytic hyperbilirubinemia (Crigler-Najjar)--report of 5 cases].
    Schellong G, Soennecken U.
    Monatsschr Kinderheilkd (1902); 1971 Jul; 119(7):422-4. PubMed ID: 5093938
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  • 15. The degradation of haem by mammals and its excretion as conjugated bilirubin.
    Lathe GH.
    Essays Biochem; 1972 Jul; 8():107-48. PubMed ID: 4564871
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  • 17. Bilirubin metabolism and inheritable jaundice.
    Arias IM.
    Isr J Med Sci; 1973 Jul; 9(9):1419-26. PubMed ID: 4775128
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