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PUBMED FOR HANDHELDS

Journal Abstract Search


344 related items for PubMed ID: 5794637

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  • 6. Screening for inborn errors of amino acid metabolism.
    Wu JT.
    Ann Clin Lab Sci; 1991; 21(2):123-42. PubMed ID: 2029175
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  • 7. Screening for hyperaminoacidemias in newborns by thin-layer chromatography on DEAE-cellulose.
    Vercaemst R, Blaton V, Lievens-Taveirne J, Peeters H.
    Acta Paediatr Belg; 1973; 27(5):334-47. PubMed ID: 4779694
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  • 8. [Multiple screening test for the detection of inborn errors of metabolism : experiment of mass-screening test with ultra-micro amino acid analysis method in dried blood spot (author's transl)].
    Sumi K, Konishi K, Shimizu S, Mimura K, Uemura I, Matsuoka A.
    Rinsho Byori; 1978 Jun; 26(6):532-6. PubMed ID: 691784
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  • 10. [Hereditary tyrosinemia. II. Presentation of a system of detection].
    Bélanger M, Saint-Hilaire B.
    Pediatrie; 1973 Jun; 28(1):19-22. PubMed ID: 4715464
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  • 11. Chemical diagnosis of amino acid abnormalities. Possibilities and desirabilities.
    Wadman SK.
    Acta Univ Carol Med Monogr; 1977 Jun; (77 Pt 1):49-69. PubMed ID: 615451
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  • 14. [Personal experience in the clinical use of free amino acids in the blood and urine].
    Borota J, Velisavljev M, Jojić M.
    Med Pregl; 1984 Jun; 37(9-10):387-91. PubMed ID: 6530984
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  • 16. Amino acid screening of mentally defective patients by high voltage electrophoresis.
    Meyer JS, Wood MJ.
    Mo Med; 1972 Feb; 69(2):112-6. PubMed ID: 5058792
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  • 19. [Organized detection of hereditary metabolic diseases. Amino acidopathies and organic acidurias].
    Kaabachi N, Mebazaa A, Hamza L, Ben Miled S, Abdelmoula J.
    Tunis Med; 1989 Nov; 67(11):697-701. PubMed ID: 2595818
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