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Journal Abstract Search

226 related items for PubMed ID: 4197345

  • 21. [Amino acid imbalance as a pathogenetic factor in mental retardation (author's transl)].
    Fekete G.
    Klin Wochenschr; 1974 May 15; 52(6):276-82. PubMed ID: 4408538
    [No Abstract] [Full Text] [Related]

  • 22. [A system of early screening for inborn errors of metabolism: methods and results for hereditary tyrosinemia].
    Bélanger M, Saint-Hilaire B, Bélanger L.
    Union Med Can; 1973 Feb 15; 102(2):294-302. PubMed ID: 4709460
    [No Abstract] [Full Text] [Related]

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  • 24. [Examination technics in metabolic brain damage with special reference to thin-layer chromatography].
    Lothaller H, Rett A, Zimprich H.
    Wien Klin Wochenschr; 1971 Nov 26; 83(47):863-6. PubMed ID: 4257065
    [No Abstract] [Full Text] [Related]

  • 25. [Problems in the detection of hereditary diseases studied in the light of frequent examples].
    Vis HL.
    Brux Med; 1972 Feb 26; 52(2):95-100. PubMed ID: 4551157
    [No Abstract] [Full Text] [Related]

  • 26.
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  • 27. [Amino acid composition in blood and urine from healthy newborn infants: screening test for the detection of enxymopathies].
    Adrienne S.
    Orv Hetil; 1969 Jun 08; 110(23):1315-20. PubMed ID: 5794637
    [No Abstract] [Full Text] [Related]

  • 28. [Hyperphenylalaninemia and other hyperaminoacidurias with mental retardation, detected by multiple screening].
    Hyánek J.
    Cas Lek Cesk; 1972 Jun 08; 111(8):176-8. PubMed ID: 5010326
    [No Abstract] [Full Text] [Related]

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  • 30. [Screening for aminoacidopathies in newborns by means of an aminoacid analyzer. Reference values and statistical determinations (author's transl)].
    Antonozzi I, Del Castello PG, Morisi G, Ceccarelli P.
    Ann Ist Super Sanita; 1978 Jun 08; 14(4):781-91. PubMed ID: 756692
    [Abstract] [Full Text] [Related]

  • 31. [Chromatographic analysis in the diagnosis of metabolic aminoacidopathies].
    Sietti C.
    Minerva Pediatr; 1971 Dec 22; 23(51):2125-8. PubMed ID: 5136312
    [No Abstract] [Full Text] [Related]

  • 32. [Study of amino-aciduria and amino-acidemia in children by chromato-ionophoresis].
    Vovan L, Perrimond H, Pierron H, Orsini A.
    Mars Med; 1967 Dec 22; 104(10):811-9. PubMed ID: 5623923
    [No Abstract] [Full Text] [Related]

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  • 37. [Transitory neonatal disorders of amino acid metabolism].
    Lambotte C, Dodinval-Versie J, Adam A.
    Rev Med Liege; 1975 Sep 01; 30(17):579-86. PubMed ID: 1166174
    [No Abstract] [Full Text] [Related]

  • 38. [Diet therapy of some inborn errors of metabolism].
    Perrone L.
    Pediatria (Napoli); 1974 Sep 30; 82(2):260-97. PubMed ID: 4473102
    [No Abstract] [Full Text] [Related]

  • 39. [Dietetics in hereditary enzyme deficiencies].
    Royer P.
    Sem Hop; 1970 Feb 26; 46(10):653-9. PubMed ID: 4314674
    [No Abstract] [Full Text] [Related]

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