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 *

249 related articles for article (PubMed ID: 5232916)

  • 1. Metabolic factors in the prevention of mental retardation. Compulsory screening legislation open to question.
    Efron ML
    R I Med J; 1967 Apr; 50(4):255-7. PubMed ID: 5232916
    [No Abstract]   [Full Text] [Related]  

  • 2. Diagnosis and treatment of metabolic errors.
    Can Med Assoc J; 1971 Jun; 104(12):1064-5. PubMed ID: 5580749
    [No Abstract]   [Full Text] [Related]  

  • 3. The Oregon program of screening for inborn errors of metabolism.
    Ashley CG
    Northwest Med; 1971 Apr; 70(4):268-9. PubMed ID: 5550115
    [No Abstract]   [Full Text] [Related]  

  • 4. Urinary screening tests in the prevention of mental deficiency.
    Perry TL; Hansen S; MacDougall L
    Can Med Assoc J; 1966 Jul; 95(3):89-95. PubMed ID: 5945986
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prevention of mental retardation through screening, retrieval, diagnosis, and management of inherited metabolic disease.
    Acosta PB
    Ala J Med Sci; 1982 Oct; 19(4 Suppl 1):10-6. PubMed ID: 7149165
    [No Abstract]   [Full Text] [Related]  

  • 6. Prevention of mental retardation: the role of medicine.
    Sells CJ; Bennett FC
    Am J Ment Defic; 1977 Sep; 82(2):117-29. PubMed ID: 71859
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Screening and therapy of 6 metabolic diseases of hereditary nature which are possible causes of mental retardation: screening of 1,900,000 newborn infants since the year 1965].
    Menne F
    Clin Ter; 1979 Mar; 88(5):445-59. PubMed ID: 466967
    [No Abstract]   [Full Text] [Related]  

  • 8. [Prevention of congenital metabolic diseases. Early diagnosis by neonatal screening].
    Giovannini M; Riva E
    Minerva Med; 1979 Mar; 70(16):1137-46. PubMed ID: 440584
    [No Abstract]   [Full Text] [Related]  

  • 9. [Diagnosis and therapy of 6 hereditary, to mental-deficiency-leading, metabolic disorders. 2].
    Menne F; Enzenauer J; Matz D
    Med Klin; 1976 Apr; 71(18):779-85. PubMed ID: 178988
    [No Abstract]   [Full Text] [Related]  

  • 10. Newborn screening for hereditary metabolic disorders in Manitoba, 1965-1970.
    Fox JG; Hall DL; Haworth JC; Maniar A; Sekla L
    Can Med Assoc J; 1971 Jun; 104(12):1085-8. PubMed ID: 5580751
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The results of chromatographic screening for the detection of inborn metabolic errors in normal and mentally retarded population.
    Hyánek J; Homolka J
    Acta Univ Carol Med Monogr; 1973; 56():63-6. PubMed ID: 4791780
    [No Abstract]   [Full Text] [Related]  

  • 12. ["Metabolic screening" of newborns and infants].
    Lakartidningen; 1968 Apr; 65(15):1518. PubMed ID: 5741859
    [No Abstract]   [Full Text] [Related]  

  • 13. Inborn errors of metabolism. A diagnostic consideration in mental retardation.
    White HH
    J Kans Med Soc; 1969 Mar; 70(3):142-5 passim. PubMed ID: 5773192
    [No Abstract]   [Full Text] [Related]  

  • 14. [Antenatal and neonatal prevention of handicaps].
    Veylon R
    Nouv Presse Med; 1979 Jun; 8(27):2296. PubMed ID: 493011
    [No Abstract]   [Full Text] [Related]  

  • 15. Pediatric continuing education. Screening for inborn errors of metabolism.
    Morrow G
    Ariz Med; 1974 Jul; 31(7):520-1. PubMed ID: 4845607
    [No Abstract]   [Full Text] [Related]  

  • 16. [Screening of newborn infants for inborn errors of metabolism].
    Halvorsen S; Skjelkvåle L
    Tidsskr Nor Laegeforen; 1970 Jan; 90(2):233-5. PubMed ID: 5430194
    [No Abstract]   [Full Text] [Related]  

  • 17. Austria newborn screening programme for inborn errors of metabolism.
    Thalhammer O
    Acta Univ Carol Med Monogr; 1973; 56():79-82. PubMed ID: 4791784
    [No Abstract]   [Full Text] [Related]  

  • 18. [Early recognition of inborn metabolic abnormalities. Methods and results of the Austrian program. II. (Conclusion)].
    Schmierer G
    Med Lab (Stuttg); 1973 May; 26(5):115-9. PubMed ID: 4709319
    [No Abstract]   [Full Text] [Related]  

  • 19. [Systematic detection of hereditary metabolic encephalopathies].
    Neimann N; Pierson M; Vidailhet M; Siest G; Badonnel Y; Humbel R; Roos F
    Ann Pediatr (Paris); 1968 Oct; 15(10):635-41. PubMed ID: 4237831
    [No Abstract]   [Full Text] [Related]  

  • 20. [Laboratory diagnosis of inborn metabolic disorders: a method for early detection of mental retardation (author's transl)].
    Zimolo A
    Lijec Vjesn; 1978 Jan; 100(1):75-6. PubMed ID: 642698
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 13.