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Journal Abstract Search

175 related items for PubMed ID: 7106768

  • 1. Intracellular phenylalanine and tyrosine concentration in homozygotes and heterozygotes for phenylketonuria (PKU) and hyperphenylalaninemia compared with normals.
    Thalhammer O, Lubec G, Königshofer H, Scheibenreiter S, Coradello H.
    Hum Genet; 1982; 60(4):320-1. PubMed ID: 7106768
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  • 2. [Intracellular concentration of phenylalanine, tyrosine and alpha-amino butyric acid in 13 homozygotes and 19 heterozygotes for phenylketonuria (PKU) compared with 26 normals (author's transl)].
    Thalhammer O, Pollak A, Lubec G, Königshofer H.
    Klin Padiatr; 1980 Nov; 192(6):608-12. PubMed ID: 7194402
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  • 3. Intracellular phenylalanine and tyrosine concentrations in 19 heterozygotes for phenylketonuria (PKU) and 26 normals. Do the higher values in heterozygotes explain their lowered intellectual level?
    Thalhammer O, Lubec G, Königshofer H.
    Hum Genet; 1979 Jul 18; 49(3):333-6. PubMed ID: 478540
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  • 6. 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 Jul 18; 4(2):73-4. PubMed ID: 6790854
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  • 8. [Phenylalanine metabolites in the urine after oral phenylalanine loading. Significance for the discrimination between classical phenylketonuria and variations of hyperphenylalaninemia (heterozygotes and homozygotes)].
    Koepp P.
    Fortschr Med; 1977 Mar 10; 95(10):627-31. PubMed ID: 844759
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  • 9. Different phenotypes for phenylalanine hydroxylase deficiency.
    Güttler F, Hansen G.
    Ann Clin Biochem; 1977 May 10; 14(3):124-34. PubMed ID: 869488
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  • 12. Compound heterozygosity in nonphenylketonuria hyperphenylalanemia: the contribution of mutations for classical phenylketonuria.
    Avigad S, Kleiman S, Weinstein M, Cohen BE, Schwartz G, Woo SL, Shiloh Y.
    Am J Hum Genet; 1991 Aug 10; 49(2):393-9. PubMed ID: 1867197
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