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Journal Abstract Search

328 related items for PubMed ID: 5580751

  • 1. 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 19; 104(12):1085-8. PubMed ID: 5580751
    [Abstract] [Full Text] [Related]

  • 2. [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 15; 88(5):445-59. PubMed ID: 466967
    [No Abstract] [Full Text] [Related]

  • 3. [Detection of hereditary metabolic diseases in Quebec].
    Grenier A, Laberge C.
    Union Med Can; 1974 Mar 15; 103(3):453-6. PubMed ID: 4820873
    [No Abstract] [Full Text] [Related]

  • 4. The place of large-scale screening in the prevention of hereditary diseases. Phenylketonuria.
    Szeinberg A, Cohen BE.
    Isr J Med Sci; 1973 Mar 15; 9(9):1319-22. PubMed ID: 4775112
    [No Abstract] [Full Text] [Related]

  • 5. [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 02; 15(10):635-41. PubMed ID: 4237831
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  • 10. Early detection of inborn errors of metabolism in Poland.
    Bozkowa K, Cabalska B, Duczynska N, Grodzka Z, Lenartowska I, Helwich E.
    Acta Anthropogenet; 1983 Oct 02; 7(4):373-81. PubMed ID: 6680316
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  • 11. Results of 10 years of screening of newborn infants for inherited metabolic diseases in the province of Limburg (Belgium).
    Greven-Brauns G, Mulkens E.
    Arch Belg Med Soc; 1979 Oct 02; 37(8):516-9. PubMed ID: 550724
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  • 12. [12 years Austrian newborn screening for inborn errors of metabolism. Results with special reference to phenylketonuria, hyperphenylalaninemia and histidinemia (author's transl)].
    Thalhammer O, Scheibenreiter S, Knoll E, Wehle E, Schön R.
    Klin Padiatr; 1980 Nov 02; 192(6):589-98. PubMed ID: 7194400
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  • 15. [Screening of newborn infants for inborn errors of metabolism].
    Halvorsen S, Skjelkvåle L.
    Tidsskr Nor Laegeforen; 1970 Jan 25; 90(2):233-5. PubMed ID: 5430194
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  • 16. [Neonatal diagnosis of hereditary metabolic diseases].
    Lambotte C.
    Rev Med Liege; 1973 Dec 15; 28(24):837-51. PubMed ID: 4769974
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  • 17. State newborn screening in the tandem mass spectrometry era: more tests, more false-positive results.
    Tarini BA, Christakis DA, Welch HG.
    Pediatrics; 2006 Aug 15; 118(2):448-56. PubMed ID: 16882794
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