These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (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; 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; 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; 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; 280():1-80. PubMed ID: 7006308
    [No Abstract]   [Full Text] [Related]  

  • 9. [Maternal phenylketonuria syndrome: teratogenic effect of hyperphenylalaninemia].
    Szabó L; Somogyi C; Máté M
    Orv Hetil; 1982 Nov; 123(47):2895-901. PubMed ID: 7177638
    [No Abstract]   [Full Text] [Related]  

  • 10. Epidemiological considerations on maternal hyperphenylalaninemia.
    Hansen H
    Am J Ment Defic; 1970 Jul; 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; 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; 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; 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; 99(4):783-814. PubMed ID: 7185286
    [No Abstract]   [Full Text] [Related]  

  • 15. Hyperphenylalaninemia in a premature infant with heterozygosity for phenylketonuria.
    Hennermann JB; Loui A; Weber A; Mönch E
    J Perinat Med; 2004; 32(4):383-5. PubMed ID: 15346830
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sex ratio in hyperphenylalaninemia.
    Berman JL
    N Engl J Med; 1970 Aug; 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; 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; 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; 10(3):258-9. PubMed ID: 9298832
    [No Abstract]   [Full Text] [Related]  

  • 20. A missense mutation (A to G) of 6-pyruvoyltetrahydropterin synthase in tetrahydrobiopterin-deficient form of hyperphenylalaninemia.
    Ashida A; Owada M; Hatakeyama K
    Genomics; 1994 Nov; 24(2):408-10. PubMed ID: 7698774
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.