BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

243 related articles for article (PubMed ID: 4775121)

  • 1. The hyperphenylalaninemias in Israel.
    Cohen BE; Szeinberg A; Pollak S; Peled I; Likverman S; Crispin M
    Isr J Med Sci; 1973; 9(9):1393-5. PubMed ID: 4775121
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Neonatal hyperphenylalaninemia: a differential diagnosis.
    Menkes JH; Holtzman NA
    Neuropadiatrie; 1970 Apr; 1(4):434-46. PubMed ID: 5538081
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. Phenylalaninaemia. Differential diagnosis.
    Blaskovics ME; Schaeffler GE; Hack S
    Arch Dis Child; 1974 Nov; 49(11):835-43. PubMed ID: 4441120
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Review of current practices in management of inherited disorders of amino acid metabolism in Western Europe.
    Wachtel U
    Hum Nutr Appl Nutr; 1986; 40 Suppl 1():61-9. PubMed ID: 3528074
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. [Phenylketonuria and hyperphenylalaninemia: clinico-genetic classification of 14 forms].
    Annenkov GA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(3):351-6. PubMed ID: 6720175
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Screening tests for phenylketonuria.
    Br Med J; 1968 Oct; 4(5622):4. PubMed ID: 4971102
    [No Abstract]   [Full Text] [Related]  

  • 10. [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]  

  • 11. [Paper samples in detection and confirmation of some anomalies of amino acid metabolism].
    Charpentier C; Lemonnier A
    Ann Biol Clin (Paris); 1969; 27(5):297-323. PubMed ID: 4897889
    [No Abstract]   [Full Text] [Related]  

  • 12. Genetic screening: notes added in proof.
    Levy HL
    Adv Hum Genet; 1973; 4():389-94. PubMed ID: 4783333
    [No Abstract]   [Full Text] [Related]  

  • 13. Recent advances in the early detection and treatment of inborn errors with brain damage.
    Bickel H
    Neuropadiatrie; 1969; 1(1):1-11. PubMed ID: 4942066
    [No Abstract]   [Full Text] [Related]  

  • 14. [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]  

  • 15. Origins of hyperphenylalaninemia in Israel.
    Kleiman S; Avigad S; Vanagaite L; Shmuelevitz A; David M; Eisensmith RC; Brand N; Schwartz G; Rey F; Munnich A; Woo SL; Shiloh Y
    Eur J Hum Genet; 1994; 2(1):24-34. PubMed ID: 7913865
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. [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]  

  • 18. [Molecular pathology and DNA diagnosis of phenylketonuria and hypermethioninemia].
    Nagao M
    Tanpakushitsu Kakusan Koso; 1998 May; 43(6):762-9. PubMed ID: 9612070
    [No Abstract]   [Full Text] [Related]  

  • 19. Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study.
    Humangenetik; 1975 Dec; 30(4):273-86. PubMed ID: 1218857
    [No Abstract]   [Full Text] [Related]  

  • 20. [Phenylketonuria. Yesterday, today and tomorrow].
    Bickel H
    Arch Fr Pediatr; 1983; 40 Suppl 1():207-13. PubMed ID: 6349571
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 13.