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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

184 related items for PubMed ID: 5557172

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  • 6. [Familial hyperlysinemia with mental retardation, convulsion & muscular hypertonia (author's transl)].
    Kobayashi T, Ueno E, Fujita T, Yanagisawa N, Tsukagoshi H.
    Rinsho Shinkeigaku; 1977 Sep; 17(9):600-8. PubMed ID: 923176
    [No Abstract] [Full Text] [Related]

  • 7. Hyperlysinemia associated with retardation.
    Ghadimi H, Binnington VI, Pecora P.
    N Engl J Med; 1965 Sep 30; 273(14):723-9. PubMed ID: 5825685
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  • 9. Chemical pathology of amino acid diseases.
    Carson NA.
    Acta Neurol Psychiatr Belg; 1968 Apr 30; 68(4):231-44. PubMed ID: 4972604
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  • 10. Inborn metabolic disorders with associated ocular lesions in Northern Ireland.
    Martin VA, Carson NA.
    Trans Ophthalmol Soc U K (1962); 1967 Apr 30; 87():847-70. PubMed ID: 5255262
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  • 11. [A patient with persistent hyperlysinemia].
    Sengers RC, Trijbels JM, Corstiaensen JB.
    Tijdschr Kindergeneeskd; 1983 Feb 30; 51(1):24-6. PubMed ID: 6407142
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  • 12. [Familial essential hyperprolinemia].
    Hainaut H, Hariga J, Willems C, Heusden A, Chapelle P.
    Presse Med (1893); 1971 Apr 24; 79(21):945-8. PubMed ID: 5580522
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  • 13. [Ocular complications of congenital metabolism errors].
    Goux JP, Kallay O.
    Bull Soc Belge Ophtalmol; 1971 Apr 24; 157(1):9-322. PubMed ID: 5565533
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  • 14. [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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  • 15. [Phaenotypic aspects of hereditary aminoacidopathies (author's transl)].
    Becker K.
    Monatsschr Kinderheilkd; 1981 Oct 31; 129(10):556-63. PubMed ID: 6801479
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  • 16. Multiple enzyme defects in familial hyperlysinemia.
    Dancis J, Hutzler J, Woody NC, Cox RP.
    Pediatr Res; 1976 Jul 31; 10(7):686-91. PubMed ID: 934735
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  • 17. [Familial hyperprolinemia with nephropathy].
    Ortuño Mirete J, Guardiola Vicente JM, Botella García J.
    Rev Clin Esp; 1970 Jul 31; 118(2):141-50. PubMed ID: 5486371
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  • 18. [Disorders of amino acids].
    Aoki K.
    Nihon Rinsho; 1993 Jan 31; 51 Suppl():332-9. PubMed ID: 8459561
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  • 19. [Maple syrup urine disease].
    Rokkones T.
    Tidsskr Nor Laegeforen; 1970 Jan 25; 90(2):239-42. PubMed ID: 5430195
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  • 20. Ocular pathology in homocystinuria.
    Henkind P, Ashton N.
    Trans Ophthalmol Soc U K (1962); 1965 Jan 25; 85():21-38. PubMed ID: 5227183
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