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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

131 related items for PubMed ID: 4886401

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. [On enzyme defects of the gastrointestinal tract].
    Diwok K.
    Z Arztl Fortbild (Jena); 1969 Jun 01; 63(11):586-90. PubMed ID: 4308889
    [No Abstract] [Full Text] [Related]

  • 3.
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  • 4. [Hereditary enzyme defects of amino acid metabolism].
    SCHULTZE-JENA BS.
    Ergeb Inn Med Kinderheilkd; 1962 Jun 01; 18():1-46. PubMed ID: 13987252
    [No Abstract] [Full Text] [Related]

  • 5.
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  • 6. Differential diagnosis and diseases due to enzyme changes.
    Martin-DeLeon PA.
    Del Med J; 1979 May 01; 51(5):267-70, 276-81. PubMed ID: 110628
    [No Abstract] [Full Text] [Related]

  • 7.
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  • 8. [The inborn errors of metabolism of amino acids].
    Tomaszewski L.
    Postepy Biochem; 1973 May 01; 19(1):91-122. PubMed ID: 4697972
    [No Abstract] [Full Text] [Related]

  • 9. Genetic screening.
    Levy HL.
    Adv Hum Genet; 1973 May 01; 4():1-104. PubMed ID: 4593296
    [No Abstract] [Full Text] [Related]

  • 10. Diet therapy for inborn errors of amino acid metabolism.
    Efron ML.
    J Am Diet Assoc; 1967 Jul 01; 51(1):40-5. PubMed ID: 6027632
    [No Abstract] [Full Text] [Related]

  • 11. A fungal perspective on human inborn errors of metabolism: alkaptonuria and beyond.
    Peñalva MA.
    Fungal Genet Biol; 2001 Oct 01; 34(1):1-10. PubMed ID: 11567547
    [Abstract] [Full Text] [Related]

  • 12. Metabolic syndromes with dermatologic manifestations.
    Irons M, Levy HL.
    Clin Rev Allergy; 1986 Feb 01; 4(1):101-24. PubMed ID: 3516355
    [No Abstract] [Full Text] [Related]

  • 13. [Pathogenesis of congenital metabolic disorders].
    Grüttner R.
    Med Klin; 1970 Aug 01; 65(32):1425-9. PubMed ID: 4943769
    [No Abstract] [Full Text] [Related]

  • 14. Screening for inborn errors of metabolism. Report of a WHO Scientific Group.
    World Health Organ Tech Rep Ser; 1968 Aug 01; 401():1-57. PubMed ID: 4973455
    [No Abstract] [Full Text] [Related]

  • 15. [Mental retardation and hereditary enzymopathy (review)].
    D'iachkova AIa, Lebedev BV.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1971 Aug 01; 71(10):1588-93. PubMed ID: 5003148
    [No Abstract] [Full Text] [Related]

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  • 17. THE PRIMARY AMINO-ACIDOPATHIES. GENETIC DEFECTS IN THE METABOLISM OF THE AMINO ACIDS.
    DIGEORGE AM, AUERBACH VH.
    Pediatr Clin North Am; 1963 Aug 01; 10():723-44. PubMed ID: 14145016
    [No Abstract] [Full Text] [Related]

  • 18.
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  • 20. Molecular mechanisms of genetic disorders of keratinization.
    Goldsmith LA.
    Arch Dermatol; 1976 Mar 01; 112(3):375-8. PubMed ID: 1259451
    [Abstract] [Full Text] [Related]

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