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Journal Abstract Search

146 related items for PubMed ID: 14332789

  • 21. Effect of phenylalanine-restricted diet in phenylketonuria. II.
    HORNER FA, STREAMER CW, CLADER DE, HASSELL LL, BINKLEY EL, DUMARS KW.
    AMA J Dis Child; 1957 Jun; 93(6):615-8. PubMed ID: 13424002
    [No Abstract] [Full Text] [Related]

  • 22. From the Clinical Conference St. Louis Children's Hospital. Phenylketonuria. Diagnostic and therapeutic dilemma.
    Kahn LI.
    Clin Pediatr (Phila); 1970 May; 9(5):263-71. PubMed ID: 5445064
    [No Abstract] [Full Text] [Related]

  • 23. A STATE PROGRAM TO CONTROL PHENYLKETONURIA.
    GROVES R, SCHLOESSER PT.
    Am J Nurs; 1964 Aug; 64():74-7. PubMed ID: 14180362
    [No Abstract] [Full Text] [Related]

  • 24. The excretion of 5-hydroxyindoleacetic acid in the heterozygous carrier for phenylketonuria.
    HSIA DY, ROWLEY WA, HUANG I.
    J Ment Defic Res; 1961 Jun; 5():4-9. PubMed ID: 13716364
    [No Abstract] [Full Text] [Related]

  • 25. MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM.
    COFFEY VP.
    J Ir Med Assoc; 1964 Mar; 54():84-7. PubMed ID: 14130648
    [No Abstract] [Full Text] [Related]

  • 26. [Biochemical and analytical bases of the exploration of phenylalanine metabolism].
    Leluc R, Lemonnier A, Charpentier C, Thuong-Cong-Trieu.
    Ann Pediatr (Paris); 1964 Mar 02; 11(3):139-46. PubMed ID: 5878702
    [No Abstract] [Full Text] [Related]

  • 27. Mental retardation in a family with phenylketonuria and mild hyperphenylalaninemia.
    Cohen BE, Szeinberg A, Berman W, Aviad Y, Crispin M, Hirshorn N, Goland R.
    Pediatrics; 1969 Nov 02; 44(5):655-60. PubMed ID: 5374976
    [No Abstract] [Full Text] [Related]

  • 28. PHENYLKETONURIA. A REVIEW OF SOME DEFICITS IN OUR INFORMATION.
    KLEINMAN DS.
    Pediatrics; 1964 Jan 02; 33():123-34. PubMed ID: 14115222
    [No Abstract] [Full Text] [Related]

  • 29. [GENETIC MENTAL DEFICIENCY].
    NODOT A.
    Rev Neuropsychiatr Infant; 1963 Jan 02; 11():433-46. PubMed ID: 14200146
    [No Abstract] [Full Text] [Related]

  • 30. Relative inability of mother and child to convert phenylalanine of tyrosine--a possible cause of nonspecific mental retardation.
    Fujimoto A, Crawford R, Bessman SP.
    Biochem Med; 1979 Jun 02; 21(3):271-6. PubMed ID: 496920
    [No Abstract] [Full Text] [Related]

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  • 32. Pyruvate metabolism by homogenates of human brain: effects of phenylpyruvate and implications for the etiology of the mental retardation in phenylketonuria.
    Patel MS, Grover WD, Auerbach VH.
    J Neurochem; 1973 Feb 02; 20(2):289-96. PubMed ID: 4698280
    [No Abstract] [Full Text] [Related]

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  • 36. ENZYMES IN MENTAL RETARDATION.
    ROSANOVA AR, NEIMEYER H, COMPALL T, MICHAELSON AS.
    IMJ Ill Med J; 1964 Jul 02; 126():52-6. PubMed ID: 14183323
    [No Abstract] [Full Text] [Related]

  • 37. [Phenylketonuria and hyperphenylalaninemia: clinico-genetic classification of 14 forms].
    Annenkov GA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984 Jul 02; 84(3):351-6. PubMed ID: 6720175
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