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Journal Abstract Search

130 related items for PubMed ID: 486619

  • 1. Screening for PKU heterozygosity in bipolar affectively ill patients.
    Targum SD, Gershon ES, Shen RS, Abell CW.
    Biol Psychiatry; 1979 Aug; 14(4):651-5. PubMed ID: 486619
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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. [The IQ of heterozygotes for phenylketonuria (PKU). indication of a blood phenylalanine-independent action of the PKU mutant (author's transl)].
    Thalhammer O, Havelec L, Knoll E, Wehle E.
    Wien Klin Wochenschr; 1977 Oct 28; 89(20):684-6. PubMed ID: 930099
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  • 4. Biochemical phenotype and its relationship with genotype in hyperphenylalaninemia heterozygotes.
    Mallolas J, Milà M, Lambruschini N, Cambra FJ, Campistol J, Vilaseca MA.
    Mol Genet Metab; 1999 Jun 28; 67(2):156-61. PubMed ID: 10356315
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  • 7. "Hypotyrosinemia" in phenylketonuria.
    Hanley WB, Lee AW, Hanley AJ, Lehotay DC, Austin VJ, Schoonheyt WE, Platt BA, Clarke JT.
    Mol Genet Metab; 2000 Apr 28; 69(4):286-94. PubMed ID: 10870846
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  • 8. [Detection of heterozygotes of typical phenylketonuria].
    Farriaux JP, Delabre M.
    Arch Fr Pediatr; 1972 Apr 28; 29(4):365-72. PubMed ID: 5053206
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  • 9. Significant phenylalanine hydroxylation in vivo in patients with classical phenylketonuria.
    Thompson GN, Halliday D.
    J Clin Invest; 1990 Jul 28; 86(1):317-22. PubMed ID: 2365821
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  • 13. Plasma biopterin levels and tetrahydrobiopterin responsiveness.
    Shintaku H, Fujioka H, Sawada Y, Asada M, Yamano T.
    Mol Genet Metab; 2005 Dec 28; 86 Suppl 1():S104-6. PubMed ID: 16183315
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  • 14. Different phenotypes for phenylalanine hydroxylase deficiency.
    Güttler F, Hansen G.
    Ann Clin Biochem; 1977 May 28; 14(3):124-34. PubMed ID: 869488
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  • 16. About changes of the phenylalanine-tyrosine metabolism in psoriasis vulgaris.
    Knapp A.
    Acta Univ Carol Med (Praha); 1986 May 28; 32(3-4):203-6. PubMed ID: 3434474
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  • 17. In vivo studies of the phenylalanine-4-hydroxylase system in hyperphenylalaninemics and phenylketonurics.
    Curtius HC, Zagalak MJ, Baerlocher K, Schaub J, Leimbacher W, Redweik U.
    Helv Paediatr Acta; 1978 Feb 28; 32(6):461-9. PubMed ID: 632110
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  • 19. 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 Feb 28; 54(2):213-6. PubMed ID: 7390492
    [No Abstract] [Full Text] [Related]

  • 20. A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria.
    Hilton MA, Sharpe JN, Hicks LG, Andrews BF.
    J Pediatr; 1986 Oct 28; 109(4):601-4. PubMed ID: 3761073
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