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Journal Abstract Search

181 related items for PubMed ID: 4257065

  • 1. [Examination technics in metabolic brain damage with special reference to thin-layer chromatography].
    Lothaller H, Rett A, Zimprich H.
    Wien Klin Wochenschr; 1971 Nov 26; 83(47):863-6. PubMed ID: 4257065
    [No Abstract] [Full Text] [Related]

  • 2. Recent advances in the early detection and treatment of inborn errors with brain damage.
    Bickel H.
    Neuropadiatrie; 1969 Nov 26; 1(1):1-11. PubMed ID: 4942066
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
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  • 4. Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders.
    Levy HL, Barkin E.
    J Lab Clin Med; 1971 Oct 26; 78(4):517-23. PubMed ID: 5114049
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
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  • 6. [5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report].
    Thalhammer O, Scheibenreiter S, Schön R, Knoll E, Schmierer G.
    Wien Klin Wochenschr; 1972 Oct 26; 84():Suppl 2:3-12. PubMed ID: 5085466
    [No Abstract] [Full Text] [Related]

  • 7. 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 Oct 26; 26 Suppl 1():130-3. PubMed ID: 8629091
    [Abstract] [Full Text] [Related]

  • 8. Thin-layer ion-exchange chromatographic screening test for aminoacidemias in blood samples dried on filter paper.
    Dévényi T, Báti J, Kovács J, Kiss P.
    Acta Biochim Biophys Acad Sci Hung; 1972 Oct 26; 7(3):237-9. PubMed ID: 4672028
    [No Abstract] [Full Text] [Related]

  • 9. [Value of the assay of urine ortho-hydroxyphenylacetic acid in hyperphenylalaninemia].
    Dhondt JL, Cartigny B, Farriaux JP.
    Ann Biol Clin (Paris); 1974 Oct 26; 32(6):499-506. PubMed ID: 4468743
    [No Abstract] [Full Text] [Related]

  • 10. 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 Oct 26; 27(5):334-47. PubMed ID: 4779694
    [No Abstract] [Full Text] [Related]

  • 11. Neonatal screening for inborn errors of amino acid metabolism.
    Levy HL.
    Clin Endocrinol Metab; 1974 Mar 26; 3(1):153-66. PubMed ID: 4609646
    [No Abstract] [Full Text] [Related]

  • 12. 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 26; 44(Pt 5):474-81. PubMed ID: 17761035
    [Abstract] [Full Text] [Related]

  • 13. Simple biochemical methods for the study of lipidoses and aminoacidopathies.
    Adriaenssens K, Karcher D.
    Riv Patol Nerv Ment; 1970 Oct 26; 91(5):274-6. PubMed ID: 5525772
    [No Abstract] [Full Text] [Related]

  • 14. The assessment of serum amino acids.
    Swallow WH, Carrell RW.
    N Z Med J; 1970 Feb 26; 71(453):85-8. PubMed ID: 5267129
    [No Abstract] [Full Text] [Related]

  • 15. Inborn errors of metabolic diseases in Malaysia: a preliminary report of maple syrup urine diseases for 1993.
    Zakiah I, Ashikin YN, Aisiah SM, Ismail HI.
    Southeast Asian J Trop Med Public Health; 1995 Feb 26; 26 Suppl 1():134-6. PubMed ID: 8629092
    [Abstract] [Full Text] [Related]

  • 16. Mild variant of maple syrup urine disease.
    Kovács J, Kiss P.
    Acta Paediatr Acad Sci Hung; 1978 Feb 26; 19(2):137-43. PubMed ID: 707084
    [Abstract] [Full Text] [Related]

  • 17. Screening for inborn errors of amino acid metabolism.
    Wu JT.
    Ann Clin Lab Sci; 1991 Feb 26; 21(2):123-42. PubMed ID: 2029175
    [Abstract] [Full Text] [Related]

  • 18. [Routine thin-layer-chromatography in 25000 newborn infants. Comparison with the Guthrie-tests].
    Schön R, Thalhammer O.
    Z Kinderheilkd; 1971 Feb 26; 111(3):223-32. PubMed ID: 5157652
    [No Abstract] [Full Text] [Related]

  • 19. Genetic screening: notes added in proof.
    Levy HL.
    Adv Hum Genet; 1973 Feb 26; 4():389-94. PubMed ID: 4783333
    [No Abstract] [Full Text] [Related]

  • 20. Screening for genetic disorders.
    Berry HK.
    Fed Proc; 1975 Nov 26; 34(12):2134-9. PubMed ID: 1102335
    [No Abstract] [Full Text] [Related]

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