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Journal Abstract Search

142 related items for PubMed ID: 5103385

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  • 3. Problems in the biochemical detection of heterozygotes for phenylketonuria.
    Yakymyshyn LY, Reid DW, Campbell DJ.
    Clin Biochem; 1972 Mar; 5(1):73-81. PubMed ID: 5022449
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  • 5. Plasma amino acid pattern in phenylketonuric heterozygotes during pregnancy.
    Cabalska B, Nowaczewska I, Duczyńska N.
    Biochem Med; 1982 Jun; 27(3):269-77. PubMed ID: 7115361
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  • 6. [Detection of heterozygotes of typical phenylketonuria].
    Farriaux JP, Delabre M.
    Arch Fr Pediatr; 1972 Apr; 29(4):365-72. PubMed ID: 5053206
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  • 7. Detection of heterozygotes for phenylketonuria by constant intravenous infusion of L-phenylalanine.
    Jagenburg R, Rödjer S.
    Clin Chem; 1977 Sep; 23(9):1661-5. PubMed ID: 890910
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  • 8. Intracellular concentrations of phenylalanine, tyrosine and alpha-aminobutyric acid in 13 homozygotes and 19 heterozygotes for phenylketonuria compared with 26 normals.
    Thalhammer O, Pollak A, Lubec G, Königshofer H.
    J Inherit Metab Dis; 1981 Sep; 4(2):73-4. PubMed ID: 6790854
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  • 9. A rapid chromatographic determination of phenylalanine and tyrosine for phenylketonuria screening.
    Mondino A, Bongiovanni G.
    J Chromatogr; 1972 Apr 26; 67(1):49-62. PubMed ID: 5024340
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  • 10. Intracellular concentrations of phenylalanine, tyrosine and alpha-aminobutyric acid in 13 homozygotes and 19 heterozygotes for phenylketonuria (PKU) compared with 26 normals.
    Thalhammer O, Pollak A, Lubec G, Königshofer H.
    Hum Genet; 1980 Apr 26; 54(2):213-6. PubMed ID: 7390492
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  • 11. Quantitative analysis of phenylalanine metabolites in urine to detect heterozygotes of phenylketonuria.
    Olek K, Oyanagi K, Wardenbach P.
    Humangenetik; 1974 Apr 24; 22(1):85-8. PubMed ID: 4837293
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  • 13. Two-dose phenylalanine tolerance test for detection of phenylketonuric heterozygotes. Value of tyrosine responses.
    ANDERSON JA, McCARTHY J, ERTEL R, FISCH R, GRAVEM H.
    J Lancet; 1961 Dec 24; 81():518-22. PubMed ID: 13861240
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  • 14. Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratio.
    Westwood A, Raine DN.
    J Med Genet; 1975 Dec 24; 12(4):327-33. PubMed ID: 1219115
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  • 16. Phenylalanine loading and aromatic acid excretion in normal subjects and heterozygotes for phenylketonuria.
    Blau K, Summer GK, Newsome HC, Edwards CH.
    Clin Chim Acta; 1973 May 18; 45(3):197-205. PubMed ID: 4708049
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  • 17. Detection of heterozygotes for phenylketonuria by column chromatography and discriminatory analysis.
    Rampini S, Anders PW, Curtius HC, Marthaler T.
    Pediatr Res; 1969 Jul 18; 3(4):287-97. PubMed ID: 5807058
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  • 20. Classic phenylketonuria: heterozygote detection during pregnancy.
    Griffin RF, Humienny ME, Hall EC, Elsas LJ.
    Am J Hum Genet; 1973 Nov 18; 25(6):646-54. PubMed ID: 4773479
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