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

168 related items for PubMed ID: 11757586

  • 1. Neonatal hypoglycaemia in severe succinyl-CoA: 3-oxoacid CoA-transferase deficiency.
    Berry GT, Fukao T, Mitchell GA, Mazur A, Ciafre M, Gibson J, Kondo N, Palmieri MJ.
    J Inherit Metab Dis; 2001 Oct; 24(5):587-95. PubMed ID: 11757586
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No 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.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Successful adaptation to ketosis by mice with tissue-specific deficiency of ketone body oxidation.
    Cotter DG, Schugar RC, Wentz AE, d'Avignon DA, Crawford PA.
    Am J Physiol Endocrinol Metab; 2013 Feb 15; 304(4):E363-74. PubMed ID: 23233542
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency.
    Song XQ, Fukao T, Mitchell GA, Kassovska-Bratinova S, Ugarte M, Wanders RJ, Hirayama K, Shintaku H, Churchill P, Watanabe H, Orii T, Kondo N.
    Biochim Biophys Acta; 1997 Apr 12; 1360(2):151-6. PubMed ID: 9128180
    [Abstract] [Full Text] [Related]

  • 13. Succinyl-CoA:acetoacetate transferase deficiency: identification of a new patient with a neonatal onset and review of the literature.
    Niezen-Koning KE, Wanders RJ, Ruiter JP, Ijlst L, Visser G, Reitsma-Bierens WC, Heymans HS, Reijngoud DJ, Smit GP.
    Eur J Pediatr; 1997 Nov 12; 156(11):870-3. PubMed ID: 9392403
    [Abstract] [Full Text] [Related]

  • 14. Ketone body metabolism and its defects.
    Fukao T, Mitchell G, Sass JO, Hori T, Orii K, Aoyama Y.
    J Inherit Metab Dis; 2014 Jul 12; 37(4):541-51. PubMed ID: 24706027
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Succinyl-CoA:3-ketoacid transferase (SCOT) deficiency in a new patient homozygous for an R217X mutation.
    Longo N, Fukao T, Singh R, Pasquali M, Barrios RG, Kondo N, Gibson KM.
    J Inherit Metab Dis; 2004 Jul 12; 27(5):691-2. PubMed ID: 15669687
    [Abstract] [Full Text] [Related]

  • 19. [Succinyl-CoA: 3-ketoacid CoA transferase deficiency].
    Fukao T.
    Ryoikibetsu Shokogun Shirizu; 1998 Jul 12; (18 Pt 1):355-8. PubMed ID: 9590068
    [No Abstract] [Full Text] [Related]

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

    Page: [Next] [New Search]
    of 9.