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Journal Abstract Search

113 related items for PubMed ID: 4765708

  • 1. Quantitative analysis of branched-chain alpha-keto acids as their trimethylsilylated oximes.
    Lancaster G, Lamm P, Scriver CR, Tjoa SS, Mamer OA.
    Clin Chim Acta; 1973 Oct 30; 48(3):279-85. PubMed ID: 4765708
    [No Abstract] [Full Text] [Related]

  • 2. Determination of alpha-keto acids as silylated oximes in urine and serum by combined gas chromatography-mass spectrometry.
    Sternowsky HJ, Roboz J, Hutterer F, Gaull G.
    Clin Chim Acta; 1973 Sep 14; 47(3):371-9. PubMed ID: 4795614
    [No Abstract] [Full Text] [Related]

  • 3. Gas-liquid chromatography of alpha-keto acids: quantification of the branched-chain-alpha-keto acids from physiological sources.
    Cree TC, Hutson SM, Harper AE.
    Anal Biochem; 1979 Jan 01; 92(1):159-63. PubMed ID: 426274
    [No Abstract] [Full Text] [Related]

  • 4. Correlations between branched-chain amino acids and branched-chain alpha-keto acids in blood in maple syrup urine disease.
    Langenbeck U, Wendel U, Mench-Hoinowski A, Kuschel D, Becker K, Przyrembel H, Bremer HJ.
    Clin Chim Acta; 1978 Sep 01; 88(2):283-91. PubMed ID: 699323
    [Abstract] [Full Text] [Related]

  • 5. Branched-chain alpha-keto acids isolated as oxime derivatives: relationship to the corresponding hydroxy acids and amino acids in maple syrup urine disease.
    Lancaster G, Mamer OA, Scriver CR.
    Metabolism; 1974 Mar 01; 23(3):257-65. PubMed ID: 4813956
    [No Abstract] [Full Text] [Related]

  • 6. Fluorescent analysis of alpha-keto acids in serum and urine by high-performance liquid chromatography.
    Koike K, Koike M.
    Anal Biochem; 1984 Sep 01; 141(2):481-7. PubMed ID: 6437276
    [Abstract] [Full Text] [Related]

  • 7. Maple syrup urine disease (branched-chain keto-aciduria) variant type manifesting as hyperkinetic behaviour and mental retardation. Report of two cases.
    Kalyanaraman K, Chamukuttan S, Arjundas G, Gajanan N, Ramamurthi B.
    J Neurol Sci; 1972 Feb 01; 15(2):209-17. PubMed ID: 5010106
    [No Abstract] [Full Text] [Related]

  • 8. [Clinical characteristics and analysis of mass spectrometric data in 33 patients with maple syrup urine disease].
    Yang N, Han LS, Ye J, Qiu WJ, Zhang HW, Gao XL, Wang Y, Li XY, Xu H, Gu XF.
    Zhonghua Yi Xue Za Zhi; 2012 Oct 30; 92(40):2839-42. PubMed ID: 23290213
    [Abstract] [Full Text] [Related]

  • 9. Prepurification and derivatization of alpha-keto acids using hydrazide gel. Application in gas chromatography and gas chromatography--mass spectrometry.
    Todoriki H, Hayashi T, Naruse H, Ikeda S.
    J Chromatogr; 1982 Nov 12; 232(2):394-9. PubMed ID: 6818241
    [No Abstract] [Full Text] [Related]

  • 10. The gas-chromatographic diagnosis of intermittent maple syrup urine disease (branch-chain ketoaciduria).
    Gompertz D, Draffan GH.
    Clin Chim Acta; 1972 Aug 12; 40(1):5-11. PubMed ID: 5056643
    [No Abstract] [Full Text] [Related]

  • 11. The relationship between the branched chain amino acids and their alpha-ketoacids in maple syrup urine disease.
    Snyderman SE, Goldstein F, Sansaricq C, Norton PM.
    Pediatr Res; 1984 Sep 12; 18(9):851-3. PubMed ID: 6483508
    [Abstract] [Full Text] [Related]

  • 12. Family with intermittent maple syrup urine disease.
    Valman HB, Patrick AD, Seakins JW, Platt JW, Gompertz D.
    Arch Dis Child; 1973 Mar 12; 48(3):225-8. PubMed ID: 4693464
    [Abstract] [Full Text] [Related]

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