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Journal Abstract Search

114 related items for PubMed ID: 4064334

  • 1. Concentrations of succinylacetone after homogentisate and tyrosine loading in healthy individuals with low fumarylacetoacetase activity.
    Kvittingen EA, Leonard JV, Pettit BR, King GS.
    Clin Chim Acta; 1985 Nov 15; 152(3):271-9. PubMed ID: 4064334
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  • 2. Succinylacetone inhibits delta-aminolevulinate dehydratase and potentiates the drug and steroid induction of delta-aminolevulinate synthase in liver.
    Sassa S, Kappas A.
    Trans Assoc Am Physicians; 1982 Nov 15; 95():42-52. PubMed ID: 7182986
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  • 3. Hereditary tyrosinemia and the heme biosynthetic pathway. Profound inhibition of delta-aminolevulinic acid dehydratase activity by succinylacetone.
    Sassa S, Kappas A.
    J Clin Invest; 1983 Mar 15; 71(3):625-34. PubMed ID: 6826727
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  • 4. ["Succinylacetone effect' after oral homogentisate loading].
    Laberge C, Lescault A, Grenier A, Gagné R.
    Union Med Can; 1981 Jul 15; 110(7):621-5. PubMed ID: 7292795
    [No Abstract] [Full Text] [Related]

  • 5. On the enzymic defects in hereditary tyrosinemia.
    Lindblad B, Lindstedt S, Steen G.
    Proc Natl Acad Sci U S A; 1977 Oct 15; 74(10):4641-5. PubMed ID: 270706
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  • 6. Hereditary tyrosinemia type I: lack of correlation between clinical findings and amount of immunoreactive fumarylacetoacetase protein.
    Kvittingen EA, Rootwelt H, van Dam T, van Faassen H, Berger R.
    Pediatr Res; 1992 Jan 15; 31(1):43-6. PubMed ID: 1594329
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  • 7. Succinylacetone and delta-aminolevulinic acid dehydratase in hereditary tyrosinemia: immunochemical study of the enzyme.
    Sassa S, Fujita H, Kappas A.
    Pediatrics; 1990 Jul 15; 86(1):84-6. PubMed ID: 2359685
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  • 8. Deficiency of fumarylacetoacetase without hereditary tyrosinemia.
    Kvittingen EA, Børresen AL, Stokke O, van der Hagen CB, Lie SO.
    Clin Genet; 1985 Jun 15; 27(6):550-4. PubMed ID: 4017276
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  • 9. Genotyping of a case of tyrosinaemia type I with normal level of succinylacetone in amniotic fluid.
    Poudrier J, Lettre F, St-Louis M, Tanguay RM.
    Prenat Diagn; 1999 Jan 15; 19(1):61-3. PubMed ID: 10073910
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  • 15. Hereditary tyrosinemia. Formation of succinylacetone-amino acid adducts.
    Manabe S, Sassa S, Kappas A.
    J Exp Med; 1985 Sep 01; 162(3):1060-74. PubMed ID: 3928801
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  • 16. Biochemical studies on the enzymatic deficiencies in hereditary tyrosinemia.
    Berger R, van Faassen H, Smith GP.
    Clin Chim Acta; 1983 Oct 31; 134(1-2):129-41. PubMed ID: 6652907
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  • 17. Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase.
    Lindstedt S, Holme E, Lock EA, Hjalmarson O, Strandvik B.
    Lancet; 1992 Oct 03; 340(8823):813-7. PubMed ID: 1383656
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  • 20. The human fumarylacetoacetase gene: characterisation of restriction fragment length polymorphisms and identification of haplotypes in tyrosinemia type 1 and pseudodeficiency.
    Rootwelt H, Kvittingen EA, Høie K, Agsteribbe E, Hartog M, van Faassen H, Berger R.
    Hum Genet; 1992 May 03; 89(2):229-33. PubMed ID: 1350265
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