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Journal Abstract Search

113 related items for PubMed ID: 4512833

  • 1.
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  • 2. 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
    [No Abstract] [Full Text] [Related]

  • 3. Phenotypic expression of galactokinase deficiency in heterozygous and homozygous subjects: in vivo and in vitro studies.
    Benson PF, Brown SP, Cree J, Fensom AH, Grant AR.
    Birth Defects Orig Artic Ser; 1976 Feb; 12(3):305-12. PubMed ID: 182297
    [Abstract] [Full Text] [Related]

  • 4. [The family of a patient with galactokinase-defect 2nd communication (author's transl)].
    Kaloud H, Sitzmann FC, Paltauf F, Mayer R.
    Klin Padiatr; 1974 Jan; 186(1):33-6. PubMed ID: 4365835
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  • 7. [The galactokinase deficiency in two human populations: Styria (Austria) and Franconia (Bavaria). A comparative investigation on gen frequency (author's transl)].
    Kaloud H, Sitzmann FC.
    Z Kinderheilkd; 1974 Feb 11; 116(3):185-91. PubMed ID: 4360413
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  • 9. Detection of heterozygotes for galactokinase deficiency in a human population.
    Mayes JS, Guthrie R.
    Biochem Genet; 1968 Nov 11; 2(3):219-30. PubMed ID: 5715186
    [No Abstract] [Full Text] [Related]

  • 10. [On the cellular distribution of catalase in the blood of homozygous and heterozygous defect-carriers (acatalasia)].
    Aebi H, Cantz M.
    Humangenetik; 1966 Nov 11; 3(1):50-63. PubMed ID: 5986055
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  • 11. [The specificity of galactokinase induction in rat liver tissue under the effect of galactose].
    Drevich VF, Salganik RI.
    Vopr Med Khim; 1975 Nov 11; 21(5):503-7. PubMed ID: 3022
    [Abstract] [Full Text] [Related]

  • 12. Amniotic-cell galactokinase activity: stimulation by galactose.
    Benson PF, Blunt S, Brown SP.
    Lancet; 1973 Jan 13; 1(7794):106-7. PubMed ID: 4118634
    [No Abstract] [Full Text] [Related]

  • 13. Cell culture in inherited disease--with some notes on genetic heterogeneity.
    Bearn AG.
    N Engl J Med; 1972 Apr 06; 286(14):764-7. PubMed ID: 4554519
    [No Abstract] [Full Text] [Related]

  • 14.
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  • 15. Properties of leukocyte catalase in Swiss type acatalasemia: a comparative study of normals, heterozygotes and homozygotes.
    Wyss SR, Aebi H.
    Enzyme; 1975 Apr 06; 20(5):257-68. PubMed ID: 811469
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  • 17. [Molecular bases of genetic enzyme diseases].
    Dreyfus JC.
    Biochimie; 1972 Apr 06; 54(5):559-71. PubMed ID: 4654152
    [No Abstract] [Full Text] [Related]

  • 18. Beta-glucuronidase deficiency mucopolysaccharidosis: methods for enzymatic diagnosis.
    Glaser JH, Sly WS.
    J Lab Clin Med; 1973 Dec 06; 82(6):969-77. PubMed ID: 4202279
    [No Abstract] [Full Text] [Related]

  • 19. Studies on erythrocyte metabolism in a case with hereditary deficiency of H-subunit of lactate dehydrogenase.
    Miwa S, Nishina T, Kakehashi Y, Kitamura M, Hiratsuka A.
    Nihon Ketsueki Gakkai Zasshi; 1971 Apr 06; 34(2):228-32. PubMed ID: 5170469
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  • 20. Prenatal diagnosis of inborn errors of metabolism.
    Mahoney MJ.
    Clin Perinatol; 1979 Sep 06; 6(2):255-73. PubMed ID: 391465
    [No Abstract] [Full Text] [Related]

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