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Journal Abstract Search

143 related items for PubMed ID: 1424246

  • 21. Aminoacidopathies: a review of 3 years experience of investigations in a Kuwait hospital.
    Yadav GC, Reavey PC.
    J Inherit Metab Dis; 1988; 11(3):277-84. PubMed ID: 3148069
    [Abstract] [Full Text] [Related]

  • 22. [Certain aspects of the biochemistry of urine in families with handicapped children].
    Petrescu L, Mogoş-Tănase I, Meilă P, Ciortoloman H.
    Physiologie; 1982; 19(2):133-41. PubMed ID: 6810393
    [No Abstract] [Full Text] [Related]

  • 23. A search for aspartylglycosaminuria in Poland.
    Galewicz A, Gorska D, Rodo M, Zaremba J.
    J Ment Defic Res; 1974 Jun; 18(2):135-7. PubMed ID: 4449118
    [No Abstract] [Full Text] [Related]

  • 24. Iherited abnormalities affecting the nervous system: genetic and psychiatric aspects.
    Stern J, Cowie V.
    Biochem J; 1969 Feb; 111(3):9P-10P. PubMed ID: 4975022
    [No Abstract] [Full Text] [Related]

  • 25. [Congenital hyperlysin-arginin-ornithinuria in a mentally retarded child (author's transl)].
    Plöchl E, Jarosch E.
    Monatsschr Kinderheilkd (1902); 1977 Oct; 125(10):892-4. PubMed ID: 917028
    [Abstract] [Full Text] [Related]

  • 26. Metabolic diseases and the skin.
    Lee EB.
    Pediatr Clin North Am; 1983 Aug; 30(4):597-608. PubMed ID: 6136951
    [No Abstract] [Full Text] [Related]

  • 27. Early detection of phenylketonuria and other aminoacidopathies in a large city using plasma chromatography.
    Raine DN.
    Arch Dis Child; 1971 Dec; 46(250):885. PubMed ID: 5129211
    [No Abstract] [Full Text] [Related]

  • 28. [A case of familial homocystinuria with carotid alterations and dislocation of the crystalline lens].
    Girard PF, Schott B, Bady B, Boucher M, David M.
    Lyon Med; 1967 Dec 03; 218(49):1369-86. PubMed ID: 5585625
    [No Abstract] [Full Text] [Related]

  • 29. [Feeble mindedness caused by genetic disorders of amino acid metabolism].
    Menne F.
    Hippokrates; 1968 May 31; 39(10):357-67. PubMed ID: 4886426
    [No Abstract] [Full Text] [Related]

  • 30. Homocystinuria and ocular defects.
    Presley GD, Sidbury JB.
    Am J Ophthalmol; 1967 Jun 31; 63(6):1723-7. PubMed ID: 6027347
    [No Abstract] [Full Text] [Related]

  • 31. [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]

  • 32. Genetic screening: notes added in proof.
    Levy HL.
    Adv Hum Genet; 1973 Oct 31; 4():389-94. PubMed ID: 4783333
    [No Abstract] [Full Text] [Related]

  • 33. Medical research council unit for metabolic studies in psychiatry, Sheffield.
    Jenner FA.
    Psychol Med; 1973 Aug 31; 3(3):379-84. PubMed ID: 4729197
    [No Abstract] [Full Text] [Related]

  • 34. Inherited metabolic disorders in Turkey.
    Ozalp I, Coskun T, Tokol S, Demircin G, Mönch E.
    J Inherit Metab Dis; 1990 Aug 31; 13(5):732-8. PubMed ID: 2246857
    [No Abstract] [Full Text] [Related]

  • 35. The pathogenesis of homocystinuria. Implications for treatment.
    Gaull GE.
    Am J Dis Child; 1967 Jan 31; 113(1):103-8. PubMed ID: 6015887
    [No Abstract] [Full Text] [Related]

  • 36. Organic acidurias and amino acidurias in the aetiology of long-term mental handicap.
    Watts RW, Baraitser M, Chalmers RA, Purkiss P.
    J Ment Defic Res; 1980 Dec 31; 24 Pt 4():257-70. PubMed ID: 6783756
    [Abstract] [Full Text] [Related]

  • 37. Inborn metabolic disorders with associated ocular lesions in Northern Ireland.
    Martin VA, Carson NA.
    Trans Ophthalmol Soc U K (1962); 1967 Dec 31; 87():847-70. PubMed ID: 5255262
    [No Abstract] [Full Text] [Related]

  • 38. Homocystinuria due to cystathionine synthase deficiency.
    Ann Intern Med; 1965 Dec 31; 63(6):1117-42. PubMed ID: 5844567
    [No Abstract] [Full Text] [Related]

  • 39. Urinary screening for abnormalities of amino acid or mucopolysaccharide metabolism in patients in a hospital for the mentally handicapped in Wessex.
    Walker V, Smythe PJ, Cook NJ, Ball NA, Veall RM, Whiteman P.
    J Ment Defic Res; 1983 Jun 31; 27 (Pt 2)():105-14. PubMed ID: 6225873
    [Abstract] [Full Text] [Related]

  • 40. Homocystinuria due to cystathionine synthase deficiency: enzymatic and ultrastructural studies.
    Gaull G, Sturman JA, Schaffner F.
    J Pediatr; 1974 Mar 31; 84(3):381-90. PubMed ID: 4811988
    [No Abstract] [Full Text] [Related]

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