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PUBMED FOR HANDHELDS

Journal Abstract Search

143 related items for PubMed ID: 4663915

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  • 2. [Methods and results of screening newborn infants for aminoacidopathies].
    Bickel H.
    Monatsschr Kinderheilkd (1902); 1976 Sep; 129(9):650-3. PubMed ID: 979984
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  • 3. [Screening newborn infants for phenylketonuria, histadinemia, homocystinuria and maple syrup disease. Results from north rhein-westphalia (1974-1976) (author's transl].
    Menne F, Otte HJ, Krüger M, Winterhoff D.
    MMW Munch Med Wochenschr; 1978 May 05; 120(18):619-22. PubMed ID: 306535
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  • 4. Neonatal screening for inborn errors of amino acid metabolism.
    Levy HL.
    Clin Endocrinol Metab; 1974 Mar 05; 3(1):153-66. PubMed ID: 4609646
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  • 5. [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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  • 7. The value of screening in paediatrics.
    Carter RA.
    J R Coll Physicians Lond; 1976 Jan 20; 10(2):153-60. PubMed ID: 54421
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  • 14. [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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  • 16. Neonatal screening in Italy for congenital hypothyroidism and metabolic disorders: hyperphenylalaninemia, maple syrup urine disease and homocystinuria.
    Antonozzi I, Dominici R, Andreoli M, Monaco F.
    J Endocrinol Invest; 1980 Jun 22; 3(4):357-63. PubMed ID: 7204885
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  • 18. [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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