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Journal Abstract Search

173 related items for PubMed ID: 615451

  • 1. Chemical diagnosis of amino acid abnormalities. Possibilities and desirabilities.
    Wadman SK.
    Acta Univ Carol Med Monogr; 1977; (77 Pt 1):49-69. PubMed ID: 615451
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  • 2. [Aminoaciduria screening in newborn infants using, comparatively, chromatographic and colorimetric methods].
    Pedrazzi AH, Rossi AR.
    Rev Farm Bioquim Univ Sao Paulo; 1976; 14(2):241-54. PubMed ID: 1030516
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  • 5. [Thin layer chromatography studies of capillary blood in newborn infants. Evaluation of utility for mass screening].
    Coradello H.
    Klin Padiatr; 1972 Sep; 184(5):358-66. PubMed ID: 4673723
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  • 10. [Mass screening of genetic metabolic abnormalities with special reference to amino acid metabolism disorders, using chemical methods].
    Lubs H, Knapp A.
    Z Arztl Fortbild (Jena); 1970 May 15; 64(10):516-9. PubMed ID: 5520559
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  • 11. Screening of amino acid enzymopathies in pregnancy and possibilities of their prenatal diagnosis.
    Hyánek J, Trnka V, Homolka J, Seemanová E, Macek M, Dolezal A, Wünschová N, Hoza J, Kapras J, Kunová V, Tauchmanová H.
    Acta Univ Carol Med Monogr; 1977 May 15; (79 Pt 3):15-21. PubMed ID: 615475
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  • 15. Screening for inborn errors of amino acid metabolism.
    Wu JT.
    Ann Clin Lab Sci; 1991 May 15; 21(2):123-42. PubMed ID: 2029175
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  • 16. [Biochemical diagnosis and mass screening for hereditary amino acid disorders].
    Owada M, Kitagawa T.
    Nihon Rinsho; 1992 Jul 15; 50(7):1522-9. PubMed ID: 1404880
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