These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

132 related items for PubMed ID: 6774167

  • 1. Intermittent non-ketotic dicarboxylic aciduria in two siblings with hypoglycaemia: an apparent defect in beta-oxidation of fatty acids.
    Naylor EW, Mosovich LL, Guthrie R, Evans JE, Tieckelmann H.
    J Inherit Metab Dis; 1980; 3(1):19-24. PubMed ID: 6774167
    [Abstract] [Full Text] [Related]

  • 2. Mitochondropathy presenting with non-ketotic hypoglycaemia as 3-hydroxydicarboxylic aciduria.
    Mayatepek E, Wanders RJ, Becker M, Bremer HJ, Hoffmann GF.
    J Inherit Metab Dis; 1995; 18(2):249-52. PubMed ID: 7564260
    [No Abstract] [Full Text] [Related]

  • 3. 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; 161():15-27. PubMed ID: 6959231
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6-C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?
    Poll-The BT, Bonnefont JP, Ogier H, Charpentier C, Pelet A, Le Fur JM, Jakobs C, Kok RM, Duran M, Divry P.
    J Inherit Metab Dis; 1988; 11 Suppl 2():183-5. PubMed ID: 2846959
    [No Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. 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
    [No Abstract] [Full Text] [Related]

  • 12. In vitro fibroblast studies in a patient with C6-C10-dicarboxylic aciduria: evidence for a defect in general acyl-CoA dehydrogenase.
    Kølvraa S, Gregersen N, Christensen E, Hobolth N.
    Clin Chim Acta; 1982 Nov 24; 126(1):53-67. PubMed ID: 7172449
    [No Abstract] [Full Text] [Related]

  • 13. 3-Hydroxydicarboxylic and 3-ketodicarboxylic aciduria in three patients: evidence for a new defect in fatty acid oxidation at the level of 3-ketoacyl-CoA thiolase.
    Bennett MJ, Sherwood WG.
    Clin Chem; 1993 May 24; 39(5):897-901. PubMed ID: 8485884
    [Abstract] [Full Text] [Related]

  • 14. 3-Hydroxydicarboxylic aciduria--a fatty acid oxidation defect with severe prognosis.
    Hagenfeldt L, von Döbeln U, Holme E, Alm J, Brandberg G, Enocksson E, Lindeberg L.
    J Pediatr; 1990 Mar 24; 116(3):387-92. PubMed ID: 2308028
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. Primary plasmalemmal carnitine transporter defect manifested with dicarboxylic aciduria and impaired fatty acid oxidation.
    Tang NL, Hui J, Law LK, To KF, Ruiter JP, IJlst L, Wanders RJ, Ho CS, Fok TF, Yuen PM, Hjelm NM.
    J Inherit Metab Dis; 1998 Jun 22; 21(4):423-5. PubMed ID: 9700600
    [No Abstract] [Full Text] [Related]

  • 17. Oxidation of fatty acids in cultured fibroblasts: a model system for the detection and study of defects in oxidation.
    Saudubray JM, Coudé FX, Demaugre F, Johnson C, Gibson KM, Nyhan WL.
    Pediatr Res; 1982 Oct 22; 16(10):877-81. PubMed ID: 7145511
    [Abstract] [Full Text] [Related]

  • 18. 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 22; 72(6):943-9. PubMed ID: 6673498
    [Abstract] [Full Text] [Related]

  • 19. [Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency].
    Collet JP, Divry P, Blanc JF, Guibaud P, David M, Macabeo V, Vibert J, Hermier M.
    Pediatrie; 1984 Dec 22; 39(8):661-8. PubMed ID: 6535973
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.