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Journal Abstract Search

276 related items for PubMed ID: 5486398

  • 1. 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
    [No Abstract] [Full Text] [Related]

  • 2. Amino acid excretion in infancy and early childhood. A survey of 200,000 infants.
    Turner B, Brown DA.
    Med J Aust; 1972 Jan 08; 1(2):62-5. PubMed ID: 5025157
    [No Abstract] [Full Text] [Related]

  • 3. [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]

  • 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 13; 15(11):64-8. PubMed ID: 4928437
    [No Abstract] [Full Text] [Related]

  • 5. [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
    [No Abstract] [Full Text] [Related]

  • 6. Screening for disorders of amino acid metabolism by thin-layer high voltage electrophoresis.
    Farrelly RO, Watkins WB.
    Clin Chim Acta; 1968 May 13; 20(2):291-4. PubMed ID: 4297715
    [No Abstract] [Full Text] [Related]

  • 7. [Further types of alkaptonuria, cystinuria and histidinemia detected in children].
    Tănase-Mogoş I, Ciortoloman H, Popescu M, Grigorescu G, Ankar V.
    Physiologie; 1979 May 13; 16(1):41-7. PubMed ID: 106416
    [No Abstract] [Full Text] [Related]

  • 8. [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]

  • 9. [Eye manifestations of amino acid disorders].
    Greco GM, Magli A.
    Minerva Pediatr; 1978 May 31; 30(10):761-80. PubMed ID: 353484
    [No Abstract] [Full Text] [Related]

  • 10. Urinary metabolic screening of mentally retarded patients from institutions in the northern part of Sweden.
    Holmgren G.
    Hum Hered; 1973 May 31; 23(6):548-60. PubMed ID: 4276001
    [No Abstract] [Full Text] [Related]

  • 11. Neonatal screening for inborn errors of amino acid metabolism.
    Levy HL.
    Clin Endocrinol Metab; 1974 Mar 31; 3(1):153-66. PubMed ID: 4609646
    [No Abstract] [Full Text] [Related]

  • 12. The assessment of serum amino acids.
    Swallow WH, Carrell RW.
    N Z Med J; 1970 Feb 31; 71(453):85-8. PubMed ID: 5267129
    [No Abstract] [Full Text] [Related]

  • 13. Recent advances in the early detection and treatment of inborn errors with brain damage.
    Bickel H.
    Neuropadiatrie; 1969 Feb 31; 1(1):1-11. PubMed ID: 4942066
    [No Abstract] [Full Text] [Related]

  • 14. Amino acid screening of mentally defective patients by high voltage electrophoresis.
    Meyer JS, Wood MJ.
    Mo Med; 1972 Feb 31; 69(2):112-6. PubMed ID: 5058792
    [No Abstract] [Full Text] [Related]

  • 15. [Attempted clinical orientation in the diagnosis of amino acid metabolism disorders. I. Urinary symptoms, neuropsychic symptoms and ocular symtpoms].
    Boisse J.
    Presse Med (1893); 1968 Apr 20; 76(19):903-6. PubMed ID: 5645352
    [No Abstract] [Full Text] [Related]

  • 16. [Aminoaciduria screening in newborn infants using, comparatively, chromatographic and colorimetric methods].
    Pedrazzi AH, Rossi AR.
    Rev Farm Bioquim Univ Sao Paulo; 1976 Apr 20; 14(2):241-54. PubMed ID: 1030516
    [Abstract] [Full Text] [Related]

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  • 18. The philosophy and practice of screening for inherited diseases.
    Komrower GM.
    Pediatrics; 1974 Feb 20; 53(2):182-8. PubMed ID: 4272866
    [No Abstract] [Full Text] [Related]

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