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PUBMED FOR HANDHELDS

Journal Abstract Search

185 related items for PubMed ID: 6466694

  • 1. Urinary excretion of dicarboxylic acids from patients with the Zellweger syndrome. Importance of peroxisomes in beta-oxidation of dicarboxylic acids.
    Björkhem I, Blomstrand S, Hågå P, Kase BF, Palonek E, Pedersen JI, Strandvik B, Wikström SA.
    Biochim Biophys Acta; 1984 Aug 15; 795(1):15-9. PubMed ID: 6466694
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  • 2. C6-C10-dicarboxylic aciduria: biochemical considerations in relation to diagnosis of beta-oxidation defects.
    Gregersen N, Kølvraa S, Mortensen PB, Rasmussen K.
    Scand J Clin Lab Invest Suppl; 1982 Aug 15; 161():15-27. PubMed ID: 6959231
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  • 4. Medium- and long-chain dicarboxylic aciduria in patients with Zellweger syndrome and neonatal adrenoleukodystrophy.
    Rocchiccioli F, Aubourg P, Bougnères PF.
    Pediatr Res; 1986 Jan 15; 20(1):62-6. PubMed ID: 3945517
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  • 6. C6--C10-dicarboxylic aciduria in starved, fat-fed and diabetic rats receiving decanoic acid or medium-chain triacylglycerol. An in vivo measure of the rate of beta-oxidation of fatty acids.
    Mortensen PB.
    Biochim Biophys Acta; 1981 May 22; 664(2):349-55. PubMed ID: 7248330
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  • 7. Urinary excretion of C4--C10-dicarboxylic acids and antiketogenic properties of adipic acid in ketogenic-stimulated rats due to diabetes, long-chain and short-chain monocarboxylic acids.
    Mortensen PB.
    Biochim Biophys Acta; 1981 May 22; 664(2):335-48. PubMed ID: 7248329
    [Abstract] [Full Text] [Related]

  • 8. Suberylglycine excretion in the urine from a patient with dicarboxylic aciduria.
    Gregersen N, Lauritzen R, Rasmussen K.
    Clin Chim Acta; 1976 Aug 02; 70(3):417-25. PubMed ID: 947635
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  • 9. Non-ketotic C6-C10-dicarboxylic aciduria: biochemical investigations of two cases.
    Gregersen N, Rosleff F, Kølvraa S, Hobolth N, Rasmussen K, Lauritzen R.
    Clin Chim Acta; 1980 Mar 28; 102(2-3):179-89. PubMed ID: 6892795
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  • 10. General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases.
    Gregersen N, Kølvraa S, Rasmussen K, Mortensen PB, Divry P, David M, Hobolth N.
    Clin Chim Acta; 1983 Aug 15; 132(2):181-91. PubMed ID: 6616873
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  • 11. The biological origin of ketotic dicarboxylic aciduria. In vivo and in vitro investigations of the omega-oxidation of C6-C16-monocarboxylic acids in unstarved, starved and diabetic rats.
    Mortensen PB, Gregersen N.
    Biochim Biophys Acta; 1981 Dec 23; 666(3):394-404. PubMed ID: 6798996
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  • 12. The biological origin of ketotic dicarboxylic aciduria. II. In vivo and in vitro investigations of the beta-oxidation of C8-C16-dicarboxylic acids in unstarved, starved and diabetic rats.
    Mortensen PB, Gregersen N.
    Biochim Biophys Acta; 1982 Mar 12; 710(3):477-84. PubMed ID: 7074126
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  • 15. Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhood.
    Divry P, David M, Gregersen N, Kølvraa S, Christensen E, Collet JP, Dellamonica C, Cotte J.
    Acta Paediatr Scand; 1983 Nov 12; 72(6):943-9. PubMed ID: 6673498
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  • 17. In vitro studies on the oxidation of medium-chain dicarboxylic acids in rat liver.
    Kølvraa S, Gregersen N.
    Biochim Biophys Acta; 1986 May 21; 876(3):515-25. PubMed ID: 3707982
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  • 19. The possible antiketogenic and gluconeogenic effect of the omega-oxidation of fatty acids in rats.
    Mortensen PB.
    Biochim Biophys Acta; 1980 Nov 07; 620(2):177-85. PubMed ID: 7437451
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