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PUBMED FOR HANDHELDS

Journal Abstract Search


119 related items for PubMed ID: 6779814

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  • 4. On the biologic origin of C6-C10-dicarboxylic and C6-C10-omega-1-hydroxy monocarboxylic acids in human and rat with acyl-CoA dehydrogenation deficiencies: in vitro studies on the omega- and omega-1-oxidation of medium-chain (C6-C12) fatty acids in human and rat liver.
    Gregersen N, Mortensen PB, Kølvraa S.
    Pediatr Res; 1983 Oct; 17(10):828-34. PubMed ID: 6634246
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  • 6. 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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  • 8. Azelaic and pimelic acids: metabolic intermediates or artefacts?
    Bennett MJ, Ragni MC, Hood I, Hale DE.
    J Inherit Metab Dis; 1992 Aug 15; 15(2):220-3. PubMed ID: 1527989
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  • 9. The excretion of C6-C10-dicarboxylic acids in the urine of newborn infants during starvation. Evidence for omega-oxidation of fatty acids in the newborn.
    Gregersen N, Ingerslev J.
    Acta Paediatr Scand; 1979 Sep 15; 68(5):677-81. PubMed ID: 525335
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  • 10. Specific and sensitive method for the determination of C6--C10 dicarboxylic acids in serum and urine by selected ion monitoring.
    Gregersen N.
    J Chromatogr; 1979 Mar 01; 162(3):377-81. PubMed ID: 528602
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  • 11. 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
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  • 12. Measurements of urinary adipic acid and suberic acid using high-performance liquid chromatography.
    Yoshioka K, Shimojo N, Nakanishi T, Naka K, Okuda K.
    J Chromatogr B Biomed Appl; 1994 May 13; 655(2):189-93. PubMed ID: 8081464
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  • 13. The absolute configuration of urinary 5-hydroxyhexanoic acid - a product of fatty acid (omega-1)-oxidation - in patients with non-ketotic dicarboxylic aciduria.
    Kamerling JP, Duran M, Bruinvis L, Ketting D, Wadman SK, Vliegenthart JF.
    Clin Chim Acta; 1982 Nov 10; 125(3):247-54. PubMed ID: 6897376
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  • 14. Excretion of 3,6-epoxydicarboxylic acids in peroxisomal disorders.
    Pitt JJ, Poulos A.
    Clin Chim Acta; 1993 Dec 31; 223(1-2):23-9. PubMed ID: 7511488
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  • 15. [Floppy female infant with congenital hydrocephalus, hepatic dysfunction and refractory convulsions].
    Nakai A.
    No To Hattatsu; 2011 Nov 31; 43(6):433-4. PubMed ID: 22180956
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  • 16. Medium- and long-chain dicarboxylic aciduria in patients with Zellweger syndrome and neonatal adrenoleukodystrophy.
    Rocchiccioli F, Aubourg P, Bougnères PF.
    Pediatr Res; 1986 Jan 31; 20(1):62-6. PubMed ID: 3945517
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  • 17. The occurrence of adipic and suberic acid in urine from ketotic patients.
    Pettersen JE, Jellum E, Eldjarn L.
    Clin Chim Acta; 1972 Apr 31; 38(1):17-24. PubMed ID: 5031780
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  • 18. 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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  • 19. Formation and degradation of dicarboxylic acids in relation to alterations in fatty acid oxidation in rats.
    Mortensen PB.
    Biochim Biophys Acta; 1992 Feb 20; 1124(1):71-9. PubMed ID: 1543729
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  • 20. A GC/MS/MS screening method for multiple organic acidemias from urine specimens.
    Hagen T, Korson MS, Sakamoto M, Evans JE.
    Clin Chim Acta; 1999 May 20; 283(1-2):77-88. PubMed ID: 10404733
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