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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

421 related items for PubMed ID: 4821497

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  • 4. [Results of screening studies for phenylketonuria, maple syrup disease and homocystinuria using Guthrie's test].
    Machill G.
    Kinderarztl Prax; 1973 May; 41(5):205-9. PubMed ID: 4732358
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  • 8. [Hereditary amino acid metabolism disorders. Indications for early diagnosis].
    Kroll S, Zebisch P, Toussaint W.
    Fortschr Med; 1972 Apr 13; 90(11):423-8. PubMed ID: 4680607
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  • 17. [Screening of the Westphalia-Lippe newborns of 1977 for phenylketonuria, histidinemia, homocystinuria and maple syrup disease. Furthermore a pilot study of galactosemia and galactokinase deficiency disease].
    Menne F, Otte HJ, Krüger M, Winterhoff D.
    MMW Munch Med Wochenschr; 1979 Jun 22; 121(25):833-4. PubMed ID: 111089
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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 Jun 22; 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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