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 *

70 related articles for article (PubMed ID: 698997)

  • 1. [Experience with diagnosing phenylalanine metabolism prior to marriage (author's transl)].
    Hyánek J; Seemanová E; Zeman L; Losan F; Salichová J; Homolka J; Viletová H; Kunová V; Matousová M; Nováková V; Kubík M; Sujanová H
    Cas Lek Cesk; 1978 Aug; 117(31):964-7. PubMed ID: 698997
    [No Abstract]   [Full Text] [Related]  

  • 2. [Early detection of inborne errors of metabolism in Switzerland: the problems of hyperphenylanalinemia (author's transl)].
    Colombo JP
    Ther Umsch; 1974 Aug; 31(8):545-52. PubMed ID: 4848540
    [No Abstract]   [Full Text] [Related]  

  • 3. [Congenital disorders of phenylalanine metabolism].
    Rampini S
    Schweiz Med Wochenschr; 1973 Apr; 103(15):537-46. PubMed ID: 4572324
    [No Abstract]   [Full Text] [Related]  

  • 4. [Difficulties in interpreting a pathological aminoaciduria].
    Farriaux JP; Dautrevaux M; Adam E; Gosselin B; Fontaine G
    Acta Paediatr Belg; 1968; 22(1):5-28. PubMed ID: 5759454
    [No Abstract]   [Full Text] [Related]  

  • 5. [Phenylalanine metabolites in the urine after oral phenylalanine loading. Significance for the discrimination between classical phenylketonuria and variations of hyperphenylalaninemia (heterozygotes and homozygotes)].
    Koepp P
    Fortschr Med; 1977 Mar; 95(10):627-31. PubMed ID: 844759
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [The use of some recent methods for diagnosis of aminoacidopathy. Personal results].
    Berio A; Di Stefano A; Bellati R; Viglione M
    Minerva Pediatr; 1971 Sep; 23(37):1519-25. PubMed ID: 5131916
    [No Abstract]   [Full Text] [Related]  

  • 7. [Value of the assay of urine ortho-hydroxyphenylacetic acid in hyperphenylalaninemia].
    Dhondt JL; Cartigny B; Farriaux JP
    Ann Biol Clin (Paris); 1974; 32(6):499-506. PubMed ID: 4468743
    [No Abstract]   [Full Text] [Related]  

  • 8. [Phenylalanine hydroxylase activity in the liver as a parameter for distinguishing various forms of hyperphenylalaninemias (author's transl)].
    Grimm U; Knapp A; Schlenzka K; Reddemann H
    Clin Chim Acta; 1975 Jan; 58(1):17-21. PubMed ID: 1122629
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Disorders of amino acid metabolism (author's transl)].
    Hirano S
    Tanpakushitsu Kakusan Koso; 1977; 22(6):776-83. PubMed ID: 337387
    [No Abstract]   [Full Text] [Related]  

  • 10. [Hyperphenylalaninemias. The Canadian and Quebec experience].
    Laberge C; Ferreira P; Grenier A; Laframbroise R; Morissette J
    Arch Fr Pediatr; 1987; 44 Suppl 1():643-7. PubMed ID: 3329493
    [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. [Phenylalanine tolerance tests].
    Mrskos A; Podhradská O
    Cesk Pediatr; 1970 Mar; 25(3):111-2. PubMed ID: 5440259
    [No Abstract]   [Full Text] [Related]  

  • 13. Molecular heterogeneity of nonphenylketonuria hyperphenylalaninemia in 25 Danish patients.
    Guldberg P; Henriksen KF; Thöny B; Blau N; Güttler F
    Genomics; 1994 May; 21(2):453-5. PubMed ID: 8088845
    [No Abstract]   [Full Text] [Related]  

  • 14. [Protein tolerance test in the differential diagnosis of inborn errors amino acid metabolism].
    Hyánek J; Viletová H; Matousová M; Kunová V; Kubík M; Soukupová Z; Tauchmanová H
    Cas Lek Cesk; 1976 Mar; 115(10):297-300. PubMed ID: 1260796
    [No Abstract]   [Full Text] [Related]  

  • 15. [Diagnosis and management of the aminoacidopathies (author's transl)].
    Farriaux JP; Dhondt JL; Cartigny B; Ardouin P
    Diabete Metab; 1978 Sep; 4(3):201-12. PubMed ID: 361464
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. [Results of screening for inborn errors of aminoacid metabolism in adult and infant patients from psychiatric institutions (author's transl)].
    Hyánek J; Turek S; Kríz J; Trísková J; Homolka J; Kopejtková H
    Cas Lek Cesk; 1975 Mar; 114(10-11):307-8. PubMed ID: 1139573
    [No Abstract]   [Full Text] [Related]  

  • 18. [Classification and heterogeneity of hyperphenylalaninemias linked to a phenylalanine hydroxylase deficiency].
    Rey F; Munnich A; Lyonnet S; Rey J
    Arch Fr Pediatr; 1987; 44 Suppl 1():639-42. PubMed ID: 3329492
    [No Abstract]   [Full Text] [Related]  

  • 19. [Malignant hyperphenylalaninemia--tetrahydrobiopterin (BH4) deficiency].
    Shintaku H
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):493-6. PubMed ID: 3270853
    [No Abstract]   [Full Text] [Related]  

  • 20. The place of large-scale screening in the prevention of hereditary diseases. Phenylketonuria.
    Szeinberg A; Cohen BE
    Isr J Med Sci; 1973; 9(9):1319-22. PubMed ID: 4775112
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.