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Journal Abstract Search

203 related items for PubMed ID: 7064884

  • 21. Neonatal screening for maple syrup urine disease by an enzyme-mediated colorimetric method.
    Wendel U, Gonzales J, Hummel W.
    Clin Chim Acta; 1993 Oct 15; 219(1-2):105-11. PubMed ID: 8306450
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  • 24. [Comparative effects of different inhibitors of phenylalanine hydroxylase and dihydropteridine reductase. In vivo and in vitro study in rats].
    Charpentier C, Domange C, Wolf M, Barthon F, Laggoune B, Lemonnier A.
    Arch Fr Pediatr; 1978 Dec 15; 35(10 Suppl):93-101. PubMed ID: 571268
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  • 25. Classical maple syrup urine disease and brain development: principles of management and formula design.
    Strauss KA, Wardley B, Robinson D, Hendrickson C, Rider NL, Puffenberger EG, Shellmer D, Moser AB, Morton DH.
    Mol Genet Metab; 2010 Apr 15; 99(4):333-45. PubMed ID: 20061171
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  • 27. Medical physiopathology, enzymology and diagnosis.
    Frézal J.
    Monogr Hum Genet; 1972 Apr 15; 6():37-49. PubMed ID: 4663914
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  • 28. New variant of phenylketonuria with progressive neurological illness unresponsive to phenylalanine restriction.
    Smith I, Clayton BE, Wolff OH.
    Lancet; 1975 May 17; 1(7916):1108-11. PubMed ID: 49470
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  • 29. Aminoacidopathies: a review of 3 years experience of investigations in a Kuwait hospital.
    Yadav GC, Reavey PC.
    J Inherit Metab Dis; 1988 May 17; 11(3):277-84. PubMed ID: 3148069
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  • 36. Development of micellar electro kinetic chromatography for the separation and quantitation of L-valine, L-leucine, L-isoleucin and L-phenylalanine in human plasma and comparison with HPLC.
    Darvish M, Ebrahimi SA, Ghadam P.
    Pak J Biol Sci; 2007 Aug 01; 10(15):2436-41. PubMed ID: 19070110
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