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Journal Abstract Search

56 related items for PubMed ID: 5174189

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  • 5. A rapid ultra performance liquid chromatography tandem mass spectrometric method for measuring amino acids associated with maple syrup urine disease, tyrosinaemia and phenylketonuria.
    Freeto S, Mason D, Chen J, Scott RH, Narayan SB, Bennett MJ.
    Ann Clin Biochem; 2007 Sep; 44(Pt 5):474-81. PubMed ID: 17761035
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  • 8. [Screening of the Westphalia-Lippe newborns of 1977 for phenylketonuria, histidinemia, homocystinuria and maple syrup disease. Furthermore a pilot study of galactosemia and galactokinase deficiency disease].
    Menne F, Otte HJ, Krüger M, Winterhoff D.
    MMW Munch Med Wochenschr; 1979 Jun 22; 121(25):833-4. PubMed ID: 111089
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  • 9. Control of pyruvate and beta-hydroxybutyrate utilization in rat brain mitochondria and its relevance to phenylketonuria and maple syrup urine disease.
    Land JM, Mowbray J, Clark JB.
    J Neurochem; 1976 Apr 22; 26(4):823-30. PubMed ID: 987160
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  • 12. RESEARCH INTO MENTAL SUBNORMALITY. 2. BIOCHEMICAL DISORDERS AND MENTAL RETARDATION.
    GIBSON J.
    Nurs Times; 1964 May 15; 60():624-5. PubMed ID: 14147186
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  • 13. DIETARY ISOLEUCINE INHIBITION OF LIVER TRYPTOPHAN HYDROXYLASE.
    YUWILER A, GELLER E, SLATER GG.
    Life Sci (1962); 1964 Jun 15; 3():567-71. PubMed ID: 14187498
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  • 16. Definition of the mutation responsible for maple syrup urine disease in Poll Shorthorns and genotyping Poll Shorthorns and Poll Herefords for maple syrup urine disease alleles.
    Dennis JA, Healy PJ.
    Res Vet Sci; 1999 Aug 15; 67(1):1-6. PubMed ID: 10425233
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  • 18. [Results of a nine-year phenylketonuria (PKU) screening (author's transl)].
    Menne F.
    MMW Munch Med Wochenschr; 1975 Jan 10; 117(2):63-8. PubMed ID: 164621
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  • 20. [Hereditary enzyme defects of amino acid metabolism].
    SCHULTZE-JENA BS.
    Ergeb Inn Med Kinderheilkd; 1962 Jan 10; 18():1-46. PubMed ID: 13987252
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