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 *

112 related articles for article (PubMed ID: 3095584)

  • 21. [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]  

  • 22. 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]  

  • 23. [Nutrition in congenital metabolic diseases].
    Plöchl E
    Padiatr Padol; 1984; 19(4):343-8. PubMed ID: 6504543
    [TBL] [Abstract][Full Text] [Related]  

  • 24. From genotype to phenotype. Free communications presented at the 31st annual meeting of the Society for the Study of Inborn Errors of Metabolism. Manchester, 7-10 September 1993.
    J Inherit Metab Dis; 1994; 17(3):257-378. PubMed ID: 7807928
    [No Abstract]   [Full Text] [Related]  

  • 25. American Academy of Pediatrics. Committee on Nutrition: special diets for infants with inborn errors of amino acid metabolism.
    Pediatrics; 1976 May; 57(5):783-92. PubMed ID: 940719
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [CONTRIBUTION TO THE STUDY OF MENTAL DEFICIENCY ETIOLOGY IN CASES OF INBORN ERRORS OF PHENYLALANINE METABOLISM].
    GONCERZEWICZ M
    Pediatr Pol; 1965 Mar; 40():259-60. PubMed ID: 14332789
    [No Abstract]   [Full Text] [Related]  

  • 27. [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]  

  • 28. [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]  

  • 29. Inborn errors of metabolism.
    Basu TK
    Nurs Times; 1970 Jan; 66(1):9-11. PubMed ID: 5410527
    [No Abstract]   [Full Text] [Related]  

  • 30. [The problem in the differential diagnosis of various forms of hyperphenylalaninemia and in its diet therapy].
    Zammarchi E
    Minerva Pediatr; 1977 Apr; 29(12):873-7. PubMed ID: 559914
    [No Abstract]   [Full Text] [Related]  

  • 31. [Problems in the detection of hereditary diseases studied in the light of frequent examples].
    Vis HL
    Brux Med; 1972 Feb; 52(2):95-100. PubMed ID: 4551157
    [No Abstract]   [Full Text] [Related]  

  • 32. [Metabolic disorders of phenylalanine and tyrosine].
    Tsukada Y; Noguchi T
    Shinkei Kenkyu No Shimpo; 1965 Jul; 9(2):217-26. PubMed ID: 5893868
    [No Abstract]   [Full Text] [Related]  

  • 33. Inborn Errors of Metabolism with Cognitive Impairment: Metabolism Defects of Phenylalanine, Homocysteine and Methionine, Purine and Pyrimidine, and Creatine.
    Sklirou E; Lichter-Konecki U
    Pediatr Clin North Am; 2018 Apr; 65(2):267-277. PubMed ID: 29502913
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Diet with inborn errors of metabolism].
    Halvorsen S; Haneborg B; Kindt E
    Tidsskr Nor Laegeforen; 1972 Sep; 92(26):1683-6. PubMed ID: 5078273
    [No Abstract]   [Full Text] [Related]  

  • 35. Phenylketonuria and other phenylalanine hydroxylation mutants in man.
    Scriver CR; Clow CL
    Annu Rev Genet; 1980; 14():179-202. PubMed ID: 7011173
    [No Abstract]   [Full Text] [Related]  

  • 36. Geographical variations in inborn errors of metabolism in Japan.
    Yasuda N
    Hum Hered; 1984; 34(1):1-8. PubMed ID: 6735410
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Phenylketonuria, the inborn errors of metabolism, and clinical research--1971.
    Epstein CJ
    Calif Med; 1971 Jul; 115(1):76-9. PubMed ID: 5566345
    [No Abstract]   [Full Text] [Related]  

  • 38. [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]  

  • 39. Inherited metabolic disease. 25 years on. Proceedings of the Silver Jubilee meeting of the Society for the Study of Inborn Errors of Metabolism. Sheffield, 22-25 September 1987.
    J Inherit Metab Dis; 1988; 11 Suppl 1():1-129. PubMed ID: 3141680
    [No Abstract]   [Full Text] [Related]  

  • 40. Inborn errors of metabolism.
    O'Brien D
    Am J Clin Nutr; 1979 Feb; 32(2):482-5. PubMed ID: 420138
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.