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Journal Abstract Search

150 related items for PubMed ID: 13431902

  • 1. Studies on conversion of phenylalanine to tyrosine in phenylpyruvic oligophrenia.
    WALLACE HW, MOLDAVE K, MEISTER A.
    Proc Soc Exp Biol Med; 1957 Apr; 94(4):632-3. PubMed ID: 13431902
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  • 2. [Some experiments on phenylalanine- and tyrosine metabolism in a patient with phenylpyruvic oligophrenia].
    HAMANN I.
    Maandschr Kindergeneeskd; 1956 Jan; 24(1):28-36. PubMed ID: 13308279
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  • 4. Aminoaciduria and mental retardation. II. Phenylpyruvic oligophrenia, phenylketonuria (PKU).
    ZELLWEGER H.
    J Iowa State Med Soc; 1961 Aug; 51():536-40. PubMed ID: 13788179
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  • 8. Phenylpyruvic oligophrenia deficiency of phenylalanine-oxidizing system.
    JERVIS GA.
    Proc Soc Exp Biol Med; 1953 Mar; 82(3):514-5. PubMed ID: 13047448
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  • 11. Inhibition of 5-hydroxytryptophan decarboxylase by phenylalanine metabolites.
    DAVISON AN, SANDLER M.
    Nature; 1958 Jan 18; 181(4603):186-7. PubMed ID: 13504122
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  • 13. [Treatment of phenylpyruvic oligophrenia].
    WOLF H.
    Medizinische; 1956 Jun 16; (24):883-6. PubMed ID: 13347861
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  • 15. The problem of phenylketonuria.
    PACHMAN DJ.
    Chic Med; 1961 Jun 17; 63():20. PubMed ID: 13731930
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  • 17. [Studies on the enzymatic and genetic system in phenylalanine metabolism disorders].
    GONCERZEWICZ M.
    Pediatr Pol; 1962 Nov 17; 37():1173-8. PubMed ID: 13948967
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  • 18. [Pathogenetic aspects of some congenital errors of metabolism].
    CUTILLO S.
    Pediatria (Napoli); 1962 Nov 17; 70():x-xvi contd. PubMed ID: 13882811
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