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Journal Abstract Search

107 related items for PubMed ID: 4765214

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  • 3. Detection of heterozygotes for aspartylglucosaminuria (AGU) in cultured fibroblasts.
    Aula P, Autio S, Raivio K, Näntö V.
    Humangenetik; 1974; 25(4):307-14. PubMed ID: 4464238
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  • 7. The biochemistry of aspartylglycosaminurias.
    Palo J, Savolainen H.
    Acta Neurol Scand Suppl; 1972; 51():483-4. PubMed ID: 4514386
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  • 8. Substrate induction of galactokinase in cultured fibroblasts from subjects heterozygous and homozygous for galactokinase deficiency.
    Zacchello F, Benson PF, Croll P, Giannelli F, Mann TP.
    Arch Dis Child; 1972 Feb; 47(251):150. PubMed ID: 5018641
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  • 10. Prenatal diagnosis and fetal pathology of aspartylglucosaminuria.
    Aula P, Rapola J, von Koskull H, Ammälä P.
    Am J Med Genet; 1984 Oct; 19(2):359-67. PubMed ID: 6507482
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  • 11. Aspartylglucosaminuria in the United States.
    Hreidarsson S, Thomas GH, Valle DL, Stevenson RE, Taylor H, McCarty J, Coker SB, Green WR.
    Clin Genet; 1983 Jun; 23(6):427-35. PubMed ID: 6883788
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  • 16. Aspartylglycosaminuria. An inborn error of metabolism associated with mental defect.
    Pollitt RJ, Jenner FA, Merskey H.
    Lancet; 1968 Aug 03; 2(7562):253-5. PubMed ID: 4173687
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  • 17. [Enzyme deficiencies detected on cultured fibroblasts and amniotic cells. Application to prenatal diagnosis].
    Dreyfus JC, Poenaru L.
    Ann Biol Clin (Paris); 1975 Aug 03; 33(6):465-72. PubMed ID: 818927
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  • 19. Disturbed metabolism of copper and zinc in aspartylglycosaminuria: possible involvement with connective tissue changes.
    Näntö-Salonen K, Halme T, Penttinen R, Langevelde FV, Vis RD, Alfthan G.
    J Inherit Metab Dis; 1985 Aug 03; 8(4):212-8. PubMed ID: 3939546
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