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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

230 related items for PubMed ID: 5025157

  • 1.
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  • 2. High-voltage electrophoresis in urinary amino acid screening.
    Holmgren G, Jeppson JO, Samuelson G.
    Scand J Clin Lab Invest; 1970 Dec; 26(4):313-8. PubMed ID: 5486398
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  • 4. [Primary and secondary hyperaminoaciduria in children (review of the literature)].
    Lebedev VP, Iur'eva EA, Mukhina IuG, Buravina TA, Koroleva IA.
    Vopr Okhr Materin Det; 1970 Nov; 15(11):64-8. PubMed ID: 4928437
    [No Abstract] [Full Text] [Related]

  • 5. Aminoacid excretion in infancy and early childhood. A survey of 100,000 infants.
    Turner B, Brown DA.
    Med J Aust; 1970 Jan 03; 1(1):11-4. PubMed ID: 5436523
    [No Abstract] [Full Text] [Related]

  • 6. [Hereditary amino acid metabolism disorders. Indications for early diagnosis].
    Kroll S, Zebisch P, Toussaint W.
    Fortschr Med; 1972 Apr 13; 90(11):423-8. PubMed ID: 4680607
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  • 8. [Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods].
    Kroll S, Zebisch P, Toussaint W.
    Fortschr Med; 1972 Apr 13; 90(11):430-1. PubMed ID: 4681731
    [No Abstract] [Full Text] [Related]

  • 9. The effect of a single oral dose of lysine or arginine on the excretion of free amino acids by the starved laying hen.
    Lee DJ.
    Br Poult Sci; 1972 Mar 13; 13(2):133-40. PubMed ID: 5017938
    [No Abstract] [Full Text] [Related]

  • 10. Problems in screening infants for defects of amino acid metabolism.
    Jackson SH.
    Clin Biochem; 1973 Mar 13; 6(1):15-21. PubMed ID: 4121648
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  • 11. [Results of a period of research (1967-1974) in the field of disorders of transport amino acid and metabolism using chromatographic, electrophoretic and dosimetric methods].
    Berio A, Allegranza A, Scapaticci E, Cadoni M, Camozzi C, Cavallo V, Di Stefano A, Santos JG.
    Minerva Pediatr; 1975 Sep 29; 27(30):1609-23. PubMed ID: 1177852
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  • 15. A prospective community survey for aminoacidaemias.
    Komrower GM, Griffiths MJ, Fowler B, Lambert AM.
    Proc R Soc Med; 1968 Mar 29; 61(3):294-6. PubMed ID: 5689917
    [No Abstract] [Full Text] [Related]

  • 16. Cystathioninuria, renal iminoglycinuria and...alpha 1-antitrypsin...deficiency in the same family: relevance in medical practice.
    Halal F, Scriver CR, Cox DW, Jaber L, Varsano I.
    Can Med Assoc J; 1979 Jul 07; 121(1):64-8. PubMed ID: 313837
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  • 20. Urinary screening for abnormalities of amino acid or mucopolysaccharide metabolism in patients in a hospital for the mentally handicapped in Wessex.
    Walker V, Smythe PJ, Cook NJ, Ball NA, Veall RM, Whiteman P.
    J Ment Defic Res; 1983 Jun 07; 27 (Pt 2)():105-14. PubMed ID: 6225873
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