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Journal Abstract Search

136 related items for PubMed ID: 5554915

  • 1. [Hyperphenylalaninemia].
    Hyánek J, Seemanová E, Sádlová I, Mrastíková H, Wünschová N, Hoza J, Zelingerová J.
    Cas Lek Cesk; 1971; 110(15):337-41. PubMed ID: 5554915
    [No Abstract] [Full Text] [Related]

  • 2. [Hyperphenylalaninemia in the neonatal period].
    Spahr A.
    Rev Med Suisse Romande; 1973 Sep; 93(9):679-86. PubMed ID: 4769047
    [No Abstract] [Full Text] [Related]

  • 3. [A mother with hyperphenylalaninemia and development of the fetus during a diet in pregnancy].
    Blehová B, Finková A, Pazoutová N.
    Cesk Gynekol; 1977 Jul; 42(6):453-4. PubMed ID: 890779
    [No Abstract] [Full Text] [Related]

  • 4. [Child of a mother with hyperphenylalaninemia].
    Hyánek J, Hoza J, Dolezal A, Vinsová N, Seemanová E, Rejmanová E.
    Cesk Pediatr; 1972 Oct; 27(10):489-91. PubMed ID: 5078514
    [No Abstract] [Full Text] [Related]

  • 5. [Offspring of mothers with hyperphenylalaninemia treated with a low phenylalanine diet before conception and during pregnancy].
    Hyánek J, Viletová H, Zeman J, Vyhnálková H, Soukup J.
    Cas Lek Cesk; 1988 Jun 03; 127(23):715-9. PubMed ID: 3401904
    [No Abstract] [Full Text] [Related]

  • 6. Biochemical factors in mental retardation.
    Hsia DY.
    Proc Annu Meet Am Psychopathol Assoc; 1967 Jun 03; 56():28-44. PubMed ID: 4966303
    [No Abstract] [Full Text] [Related]

  • 7. Inborn errors of metabolism-the relationship of clinical and biochemical abnormalities.
    Harper PS.
    Acta Univ Carol Med Monogr; 1973 Jun 03; 56():159-67. PubMed ID: 4151599
    [No Abstract] [Full Text] [Related]

  • 8. Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood.
    Güttler F.
    Acta Paediatr Scand Suppl; 1980 Jun 03; 280():1-80. PubMed ID: 7006308
    [No Abstract] [Full Text] [Related]

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  • 10. Epidemiological considerations on maternal hyperphenylalaninemia.
    Hansen H.
    Am J Ment Defic; 1970 Jul 03; 75(1):22-6. PubMed ID: 5428284
    [No Abstract] [Full Text] [Related]

  • 11. Inborn errors of metabolism. Variability within single diseases.
    Danks DM.
    Clin Pediatr (Phila); 1971 Jan 03; 10(1):1-3. PubMed ID: 5545904
    [No Abstract] [Full Text] [Related]

  • 12. [Pregnancy hyperphenylalanemia and its diagnostic importance (author's transl)].
    Hyánek J, Trnka V, Homolka J, Seemanová E, Macek M, Cervenka J, Nevsímalová S, Dolezal A, Wünschová N, Hoza J, Kapras J, Kunová V, Tauchmanová H.
    Cas Lek Cesk; 1975 Apr 25; 114(17):515-8. PubMed ID: 1131842
    [No Abstract] [Full Text] [Related]

  • 13. Hyperphenylalaninemia (PKU) and hypothyroid testing.
    Stanage WF, Gregg JB.
    S D J Med; 1982 Jul 25; 35(7):8. PubMed ID: 6958065
    [No Abstract] [Full Text] [Related]

  • 14. [Congenital errors of metabolism: phenylketonuria and hyperphenylalanemias].
    Laguna Serrano C.
    An R Acad Nac Med (Madr); 1982 Jul 25; 99(4):783-814. PubMed ID: 7185286
    [No Abstract] [Full Text] [Related]

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  • 16. Sex ratio in hyperphenylalaninemia.
    Berman JL.
    N Engl J Med; 1970 Aug 27; 283(9):491. PubMed ID: 5434125
    [No Abstract] [Full Text] [Related]

  • 17. The use of N-ethyl-N-nitrosourea to produce mouse models for human phenylketonuria and hyperphenylalaninemia.
    McDonald JD, Bode VC, Dove WF, Shedlovsky A.
    Prog Clin Biol Res; 1990 Aug 27; 340C():407-13. PubMed ID: 2381939
    [No Abstract] [Full Text] [Related]

  • 18. Phenylalanine tolerance tests. In families with phenylketonuria and hyperphenylalaninemia.
    Cunningham GC, Day RW, Berman JL, Hsia DY.
    Am J Dis Child; 1969 Jun 27; 117(6):626-35. PubMed ID: 5771502
    [No Abstract] [Full Text] [Related]

  • 19. Mutations of the phenylalanine hydroxylase gene in mild hyperphenylalaninemia: a novel mutation in exon 3.
    Zekanowski C, Cabalska B, Borsuk P, Bal J.
    Hum Mutat; 1997 Jun 27; 10(3):258-9. PubMed ID: 9298832
    [No Abstract] [Full Text] [Related]

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