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Journal Abstract Search

451 related items for PubMed ID: 6026878

  • 1. Diagnosis and treatment: interpreting the positive screening test in the newborn infant.
    Scriver CR.
    Pediatrics; 1967 May; 39(5):764-8. PubMed ID: 6026878
    [No Abstract] [Full Text] [Related]

  • 2. [Diagnosis and therapy of 6 inherited, metabolic diseases, leading to mental deficiency. 1].
    Menne F, Enzenauer J, Matz D.
    Med Klin; 1976 Apr 23; 71(17):724-8. PubMed ID: 775276
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  • 4. [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
    [No Abstract] [Full Text] [Related]

  • 5. [Screening for congenital metabolic disorders].
    Knapp A, Machill G.
    Kinderarztl Prax; 1974 Jun 25; 42(6):270-7. PubMed ID: 4610264
    [No Abstract] [Full Text] [Related]

  • 6. Screening for inborn errors of metabolism. Report of a WHO Scientific Group.
    World Health Organ Tech Rep Ser; 1968 Jun 25; 401():1-57. PubMed ID: 4973455
    [No Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Neonatal hyperphenylalaninemia: a differential diagnosis.
    Menkes JH, Holtzman NA.
    Neuropadiatrie; 1970 Apr 19; 1(4):434-46. PubMed ID: 5538081
    [No Abstract] [Full Text] [Related]

  • 9. [Neonatal diagnosis of hereditary metabolic diseases].
    Lambotte C.
    Rev Med Liege; 1973 Dec 15; 28(24):837-51. PubMed ID: 4769974
    [No Abstract] [Full Text] [Related]

  • 10. Austria newborn screening programme for inborn errors of metabolism.
    Thalhammer O.
    Acta Univ Carol Med Monogr; 1973 Dec 15; 56():79-82. PubMed ID: 4791784
    [No Abstract] [Full Text] [Related]

  • 11. [Combined forms of metabolic errors detected in newborn infants].
    Tănase-Mogoş I, Ciortoloman H, Grigorescu G, Popescu M, Ankăr V.
    Physiologie; 1978 Dec 15; 15(4):239-43. PubMed ID: 106407
    [No Abstract] [Full Text] [Related]

  • 12. [Screening of 80,000 newborn infants at delivery, for amino acid metabolism].
    Greven-Brauns G, Mulkens E.
    Arch Belg Med Soc; 1975 Apr 15; 33(4):253-7. PubMed ID: 1231644
    [No Abstract] [Full Text] [Related]

  • 13. [Early diagnosis of congenital disorders].
    Méhes K.
    Orv Hetil; 1978 Jul 23; 119(30):1819-23. PubMed ID: 353640
    [No Abstract] [Full Text] [Related]

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  • 17. [Methods and results of screening newborn infants for aminoacidopathies].
    Bickel H.
    Monatsschr Kinderheilkd (1902); 1976 Sep 23; 129(9):650-3. PubMed ID: 979984
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  • 20. [Detections tests for newborn infants].
    Paunier L.
    Rev Med Suisse Romande; 1981 May 23; 101(5):359-62. PubMed ID: 7291827
    [No Abstract] [Full Text] [Related]

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