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PUBMED FOR HANDHELDS

Journal Abstract Search


136 related items for PubMed ID: 731965

  • 1. [Screening method for the detection of urine with inherited basic amino acidopathies by thin-layer chromatography (author's transl)].
    Fukaya J, Iwase M, Kanno T.
    Rinsho Byori; 1978 Nov; 26(11):979-82. PubMed ID: 731965
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  • 2. [Development of a routine screening procedure for hyperaminoacidemias in the newborn infants, using microcrystalline cellulose thin-layer chromatography (author's transl)].
    Koide A, Kawai T.
    Rinsho Byori; 1974 Jul; 22(7):507-10. PubMed ID: 4475457
    [No Abstract] [Full Text] [Related]

  • 3. High performance liquid chromatography (HPLC) method for confirming thin layer chromatography (TLC) findings in inborn errors of metabolism children in Malaysia.
    Yahya NA, Ismail Z, Embong KH, Mohamad SA.
    Southeast Asian J Trop Med Public Health; 1995 Jul; 26 Suppl 1():130-3. PubMed ID: 8629091
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  • 4. [Thin layer chromatography of amino acids in biological medium. Use for detection and diagnosis of amino acidopathies].
    Kutter D, Humbel R.
    Pharm Acta Helv; 1970 Sep; 45(9):553-63. PubMed ID: 5469385
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  • 6. Screening for inborn errors of amino acid metabolism.
    Wu JT.
    Ann Clin Lab Sci; 1991 Sep; 21(2):123-42. PubMed ID: 2029175
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  • 11. [A simple thin layer chromatography screening test for the detection of hyperaminoacidemias].
    Kraffczyk F, Helger R, Lang H.
    Z Klin Chem Klin Biochem; 1970 Sep 08; 7(5):521-4. PubMed ID: 5505964
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  • 13. Quantitative evaluation of thin-layer ion-exchange chromatograms by video-densitometry II. Screening test for amino-acidaemias in blood samples dried on filter paper.
    Pongor S, Kovács J, Dévényi T.
    Acta Biochim Biophys Acad Sci Hung; 1978 Sep 08; 13(3):117-21. PubMed ID: 754443
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  • 15. [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 08; 26(6):532-6. PubMed ID: 691784
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  • 17. [Simultaneous thin-layer chromatography of blood and urine samples for the diagnosis of hereditary amino acid metabolism disorders].
    Peters WH, Lubs H, Knapp A.
    Z Arztl Fortbild (Jena); 1974 Jul 15; 68(14):716-25. PubMed ID: 4216183
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  • 18. [Thin layer chromatographic determination of amino acids in urine as a contribution to clinical diagnosis].
    Menzel K, Koslowski H, Fiehring C, Wedekind U, Jung G.
    Acta Paediatr Acad Sci Hung; 1971 Jul 15; 12(3):295-304. PubMed ID: 5148791
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