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Pubmed for Handhelds

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Journal Abstract Search

510 related items for PubMed ID: 14285451

  • 21. Cystathioninuria.
    Shaw KN, Lieberman E, Koch R, Donnell GN.
    Am J Dis Child; 1967 Jan; 113(1):119-28. PubMed ID: 4289134
    [No Abstract] [Full Text] [Related]

  • 22. A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.
    EFRON ML, YOUNG D, MOSER HW, MACCREADY RA.
    N Engl J Med; 1964 Jun 25; 270():1378-83. PubMed ID: 14152868
    [No Abstract] [Full Text] [Related]

  • 23. Recent work on phenylketonuria and maple syrup urine disease (leucinosis).
    WOOLF LI.
    Proc R Soc Med; 1962 Oct 25; 55(10):824-6. PubMed ID: 14001839
    [No Abstract] [Full Text] [Related]

  • 24. [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 25; 84():Suppl 2:3-12. PubMed ID: 5085466
    [No Abstract] [Full Text] [Related]

  • 25. Screening for inborn errors of metabolism. Report of a WHO Scientific Group.
    World Health Organ Tech Rep Ser; 1968 Oct 25; 401():1-57. PubMed ID: 4973455
    [No Abstract] [Full Text] [Related]

  • 26. Genetic screening: notes added in proof.
    Levy HL.
    Adv Hum Genet; 1973 Oct 25; 4():389-94. PubMed ID: 4783333
    [No Abstract] [Full Text] [Related]

  • 27. State screening for metabolic disorders in newborns.
    Stevens MB, Rigilano JC, Wilson CC.
    Am Fam Physician; 1988 Apr 25; 37(4):223-8. PubMed ID: 3358346
    [Abstract] [Full Text] [Related]

  • 28. HIGH-RESOLUTION SCREENING OF AMINO-ACIDURIAS.
    SAMUELS S.
    Arch Neurol; 1964 Mar 25; 10():322-6. PubMed ID: 14106988
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. [Methods and results of screening newborn infants for aminoacidopathies].
    Bickel H.
    Monatsschr Kinderheilkd (1902); 1976 Sep 25; 129(9):650-3. PubMed ID: 979984
    [No Abstract] [Full Text] [Related]

  • 31. [Diet therapy of inborn errors of metabolism].
    Schaub J, Bremer HJ.
    Med Klin; 1970 Aug 01; 65(32):1429-35. PubMed ID: 4943770
    [No Abstract] [Full Text] [Related]

  • 32. [Screening results for inborn errors of metabolism in Western Europe].
    Schmid-Rüter E.
    Monatsschr Kinderheilkd (1902); 1973 May 01; 121(5):205-6. PubMed ID: 4713391
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
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  • 34. METABOLIC ERRORS AND SEIZURES.
    STEMMERMANN MG.
    Epilepsia; 1965 Mar 01; 6():16-23. PubMed ID: 14302043
    [No Abstract] [Full Text] [Related]

  • 35. Collective results of mass screening for inborn metabolic errors in eight European countries.
    Acta Paediatr Scand; 1973 Jul 01; 62(4):413-6. PubMed ID: 4729691
    [No Abstract] [Full Text] [Related]

  • 36.
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  • 37. [Combined forms of metabolic errors detected in newborn infants].
    Tănase-Mogoş I, Ciortoloman H, Grigorescu G, Popescu M, Ankăr V.
    Physiologie; 1978 Jul 01; 15(4):239-43. PubMed ID: 106407
    [No Abstract] [Full Text] [Related]

  • 38. [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
    [No Abstract] [Full Text] [Related]

  • 39.
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  • 40. [Screening newborn infants for phenylketonuria, histadinemia, homocystinuria and maple syrup disease. Results from north rhein-westphalia (1974-1976) (author's transl].
    Menne F, Otte HJ, Krüger M, Winterhoff D.
    MMW Munch Med Wochenschr; 1978 May 05; 120(18):619-22. PubMed ID: 306535
    [Abstract] [Full Text] [Related]

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