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Journal Abstract Search

421 related items for PubMed ID: 4821497

  • 1. [A screening test for phenylketonuria using a paper chromatography method].
    Halvorsen S, Skjelkvåle L.
    Lakartidningen; 1974 Mar 20; 71(12):1166-7. PubMed ID: 4821497
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  • 3. Neonatal screening for inborn errors of amino acid metabolism.
    Levy HL.
    Clin Endocrinol Metab; 1974 Mar 20; 3(1):153-66. PubMed ID: 4609646
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  • 5. Recent advances in the early detection and treatment of inborn errors with brain damage.
    Bickel H.
    Neuropadiatrie; 1969 Mar 20; 1(1):1-11. PubMed ID: 4942066
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  • 10. [Paper chromatography in the detection of aminoacidopathies].
    Sietti C.
    Minerva Pediatr; 1971 Dec 22; 23(51):2123-4. PubMed ID: 5136311
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  • 12. [Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods].
    Kroll S, Zebisch P, Toussaint W.
    Fortschr Med; 1972 Apr 13; 90(11):430-1. PubMed ID: 4681731
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  • 13. [Early diagnosis of phenylketonuria, homocystinuria and maple syrup urine disease in the GDR with the aid of Gatri's microbiological inhibitor test].
    Makhill G, Knapp A.
    Pediatriia; 1974 Dec 13; (12):27-30. PubMed ID: 4614217
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  • 19. [5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report].
    Thalhammer O, Scheibenreiter S, Schön R, Knoll E, Schmierer G.
    Wien Klin Wochenschr; 1972 Dec 13; 84():Suppl 2:3-12. PubMed ID: 5085466
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  • 20. [Phenylalanine metabolites in the urine after oral phenylalanine loading. Significance for the discrimination between classical phenylketonuria and variations of hyperphenylalaninemia (heterozygotes and homozygotes)].
    Koepp P.
    Fortschr Med; 1977 Mar 10; 95(10):627-31. PubMed ID: 844759
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