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Journal Abstract Search

114 related items for PubMed ID: 4406782

  • 1. Urinary metabolic studies in hereditary macular degeneration.
    Holmgren G, Nordström S, Thorburn W.
    Acta Ophthalmol (Copenh); 1974; 52(2):225-30. PubMed ID: 4406782
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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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  • 5. A variant form of branched-chain keto aciduria.
    van der Horst JL, Wadman SK.
    Acta Paediatr Scand; 1971 Sep; 60(5):594-9. PubMed ID: 5125167
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  • 8. Investigation of ketoacidurias by two-dimensional paper chromatography.
    Coward RF, Smith P, Seakins JW.
    J Clin Pathol; 1969 Jul; 22(4):422-6. PubMed ID: 5808092
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  • 9. Screening for disorders of amino acid metabolism by thin-layer high voltage electrophoresis.
    Farrelly RO, Watkins WB.
    Clin Chim Acta; 1968 May; 20(2):291-4. PubMed ID: 4297715
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  • 11. Quantitative measurement of individual free amino acids in urine by means of high voltage paper electrophoresis. Investigations of a group of mentally retarded patients.
    Juul P.
    Scand J Clin Lab Invest; 1966 May; 18(6):629-37. PubMed ID: 5959318
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  • 15. Urinary amino acid patterns in simple and complicated bilharziasis.
    Soliman L, Abdel Kader MM, Ata AA, Abdel Wahab F, Emara SH.
    J Trop Med Hyg; 1969 Jul; 72(7):166-70. PubMed ID: 5795955
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  • 16. Hereditary vitelliform macular degeneration: variable fundus findings within a single pedigree.
    Maloney WF, Robertson DM, Duboff SM.
    Arch Ophthalmol; 1977 Jun; 95(6):979-83. PubMed ID: 869756
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  • 20. Urinary excretion of alpha-keto acids in phenylketonuria.
    ZELNICEK E.
    Clin Chim Acta; 1962 Jul; 7():592-3. PubMed ID: 14010101
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