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Journal Abstract Search

395 related items for PubMed ID: 4680607

  • 1. [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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  • 3. [Eye manifestations of amino acid disorders].
    Greco GM, Magli A.
    Minerva Pediatr; 1978 May 31; 30(10):761-80. PubMed ID: 353484
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  • 8. [Feeble mindedness caused by genetic disorders of amino acid metabolism].
    Menne F.
    Hippokrates; 1968 May 31; 39(10):357-67. PubMed ID: 4886426
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  • 10. [Phaenotypic aspects of hereditary aminoacidopathies (author's transl)].
    Becker K.
    Monatsschr Kinderheilkd; 1981 Oct 31; 129(10):556-63. PubMed ID: 6801479
    [Abstract] [Full Text] [Related]

  • 11. Recent advances in the early detection and treatment of inborn errors with brain damage.
    Bickel H.
    Neuropadiatrie; 1969 Oct 31; 1(1):1-11. PubMed ID: 4942066
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  • 12. [Primary and secondary hyperaminoaciduria in children (review of the literature)].
    Lebedev VP, Iur'eva EA, Mukhina IuG, Buravina TA, Koroleva IA.
    Vopr Okhr Materin Det; 1970 Nov 31; 15(11):64-8. PubMed ID: 4928437
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  • 13. [The inborn errors of metabolism of amino acids].
    Tomaszewski L.
    Postepy Biochem; 1973 Nov 31; 19(1):91-122. PubMed ID: 4697972
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  • 16. [Dietetics in hereditary enzyme deficiencies].
    Royer P.
    Sem Hop; 1970 Feb 26; 46(10):653-9. PubMed ID: 4314674
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  • 17. The dietary therapy of inherited metabolic disease.
    Snyderman SE.
    Prog Food Nutr Sci; 1975 Feb 26; 1(7-8):507-30. PubMed ID: 57628
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  • 18. Genetic screening: notes added in proof.
    Levy HL.
    Adv Hum Genet; 1973 Feb 26; 4():389-94. PubMed ID: 4783333
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  • 19. [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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