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

144 related items for PubMed ID: 2198431

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. In vivo propionate oxidation as a prognostic indicator in disorders of propionate metabolism.
    Thompson GN, Walter JH, Bresson JL, Bonnefont JP, Saudubray JM, Leonard JV, Halliday D.
    Eur J Pediatr; 1990 Mar; 149(6):408-11. PubMed ID: 2332010
    [Abstract] [Full Text] [Related]

  • 3. Protein and leucine metabolism in maple syrup urine disease.
    Thompson GN, Bresson JL, Pacy PJ, Bonnefont JP, Walter JH, Leonard JV, Saudubray JM, Halliday D.
    Am J Physiol; 1990 Apr; 258(4 Pt 1):E654-60. PubMed ID: 2185648
    [Abstract] [Full Text] [Related]

  • 4. Stable isotope studies in propionic and methylmalonic acidaemia.
    Leonard JV.
    Eur J Pediatr; 1997 Aug; 156 Suppl 1():S67-9. PubMed ID: 9266219
    [Abstract] [Full Text] [Related]

  • 5. Substrate disposal in metabolic disease: a comparison between rates of in vivo propionate oxidation and urinary metabolite excretion in children with methylmalonic acidemia.
    Thompson GN, Walter JH, Bresson JL, Ford GC, Bonnefont JP, Chalmers RA, Saudubray JM, Leonard JV, Halliday D.
    J Pediatr; 1989 Nov; 115(5 Pt 1):735-9. PubMed ID: 2809905
    [Abstract] [Full Text] [Related]

  • 6. The dietary therapy of inherited metabolic disease.
    Snyderman SE.
    Prog Food Nutr Sci; 1975 Nov; 1(7-8):507-30. PubMed ID: 57628
    [No Abstract] [Full Text] [Related]

  • 7. Contribution of odd-chain fatty acid oxidation to propionate production in disorders of propionate metabolism.
    Sbaï D, Narcy C, Thompson GN, Mariotti A, Poggi F, Saudubray JM, Bresson JL.
    Am J Clin Nutr; 1994 Jun; 59(6):1332-7. PubMed ID: 8198058
    [Abstract] [Full Text] [Related]

  • 8. Assessment of whole body L-leucine oxidation by noninvasive L-[1-13C]leucine breath tests: a reappraisal in patients with maple syrup urine disease, obligate heterozygotes, and healthy subjects.
    Schadewaldt P, Bodner A, Brösicke H, Hammen HW, Wendel U.
    Pediatr Res; 1998 May; 43(5):592-600. PubMed ID: 9585004
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Metabolism of 1-13C-propionate in vivo in patients with disorders of propionate metabolism.
    Barshop BA, Yoshida I, Ajami A, Sweetman L, Wolff JA, Sweetman FR, Prodanos C, Smith M, Nyhan WL.
    Pediatr Res; 1991 Jul; 30(1):15-22. PubMed ID: 1909779
    [Abstract] [Full Text] [Related]

  • 12. [Molecular biologic aspects in dermatology demonstrated by some hereditary enzyme defects].
    Balda BR, Lukacs I.
    Z Haut Geschlechtskr; 1968 Dec 01; 43(23):963-72. PubMed ID: 4886401
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Contribution of aminoacid catabolism to propionate production in methylmalonic acidaemia.
    Walter JH, Thompson GN, Leonard JV, Bartlett K, Halliday D.
    Lancet; 1989 Jun 10; 1(8650):1298-9. PubMed ID: 2566828
    [Abstract] [Full Text] [Related]

  • 15. Metabolism of branched-chain amino acids in maple syrup urine disease.
    Schadewaldt P, Wendel U.
    Eur J Pediatr; 1997 Aug 10; 156 Suppl 1():S62-6. PubMed ID: 9266218
    [Abstract] [Full Text] [Related]

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

  • 17. The need of essential amino acids in children. An evaluation based on the intake of phenylalanine, tyrosine, leucine, isoleucine, and valine in children with phenylketonuria, tyrosine amino transferase defect, and maple syrup urine disease.
    Kindt E, Halvorsen S.
    Am J Clin Nutr; 1980 Feb 10; 33(2):279-86. PubMed ID: 6101930
    [Abstract] [Full Text] [Related]

  • 18. Decreased essential amino acid requirements without catabolism in phenylketonuria and maple syrup urine disease.
    Ruch T, Kerr D.
    Am J Clin Nutr; 1982 Feb 10; 35(2):217-28. PubMed ID: 7064884
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

    Page: [Next] [New Search]
    of 8.