Compounds > succinylacetone
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succinylacetone and succinylacetoacetate

succinylacetone has been researched along with succinylacetoacetate in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19905 (83.33)18.7374
1990's1 (16.67)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hjalmarson, O; Holme, E; Lindstedt, S; Lock, EA; Strandvik, B1
Berger, R; Schierbeek, H1
Ascher, N; Bloomer, JR; Freese, DK; Ramnaraine, ML; Sharp, HL; Tuchman, M1
Berger, R; Bruinvis, L; Cartigny, B; Divry, P; Duran, M; Farriaux, JP; Ketting, D; Leonard, JV; Smit, GP; Steinmann, B; van Sprang, FJ; Wadman, SK1
Lindblad, B; Steen, G1
Fällström, SP; Lindblad, B; Steen, G1

Other Studies

6 other study(ies) available for succinylacetone and succinylacetoacetate

ArticleYear
Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase.
    Lancet (London, England), 1992, Oct-03, Volume: 340, Issue:8823

    Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Acetoacetates; alpha-Fetoproteins; Amino Acid Metabolism, Inborn Errors; Aminolevulinic Acid; Child; Child, Preschool; Cyclohexanones; Erythrocytes; Heptanoates; Humans; Hydroxybenzoates; Infant; Kidney Tubules; Liver; Nitrobenzoates; Phenylalanine; Phosphates; Porphobilinogen Synthase; Proteinuria; Tyrosine

1992
Determination of succinylacetone and succinylacetoacetate in physiological samples as the common product 5(3)-methyl-3(5)-isoxazole propionic acid using an isotope dilution method and mass spectrometry.
    Clinica chimica acta; international journal of clinical chemistry, 1989, Oct-16, Volume: 184, Issue:3

    Topics: Acetoacetates; Gas Chromatography-Mass Spectrometry; Heptanoates; Heptanoic Acids; Humans; Isotopes; Isoxazoles; Mass Spectrometry; Nitrogen Isotopes; Oxazoles; Tyrosine

1989
Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantation.
    The Journal of pediatrics, 1987, Volume: 110, Issue:3

    Topics: Acetoacetates; Amino Acid Metabolism, Inborn Errors; Aminolevulinic Acid; Child, Preschool; Female; Heptanoates; Humans; Infant; Liver Transplantation; Male; Porphobilinogen Synthase; Tyrosine

1987
Urinary excretion of deuterated metabolites in patients with tyrosinemia type I after oral loading with deuterated L-tyrosine.
    Clinica chimica acta; international journal of clinical chemistry, 1983, May-30, Volume: 130, Issue:2

    Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Acetoacetates; Amino Acid Metabolism, Inborn Errors; Deuterium; Female; Heptanoates; Heptanoic Acids; Humans; Hydrolases; Infant; Liver; Male; Tyrosine

1983
Identification of 4,6-dioxoheptanoic acid (succinylacetone), 3,5-dioxooctanedioic acid (succinylacetoacetate) and 4-Oxo-6-hydroxyheptanoic acid in the urine from patients with hereditary tyrosinemia.
    Biomedical mass spectrometry, 1982, Volume: 9, Issue:10

    Topics: Acetoacetates; Amino Acid Metabolism, Inborn Errors; Gas Chromatography-Mass Spectrometry; Heptanoates; Heptanoic Acids; Humans; Tyrosine

1982
On the renal tubular damage in hereditary tyrosinemia and on the formation of succinylacetoacetate and succinylacetone.
    Acta paediatrica Scandinavica, 1981, Volume: 70, Issue:3

    Topics: Acetoacetates; Amino Acid Metabolism, Inborn Errors; Aminolevulinic Acid; Child; Heptanoates; Homogentisic Acid; Humans; Infant; Keto Acids; Kidney Diseases; Kidney Tubules; Male; Phenylalanine; Proteinuria; Tyrosine

1981