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Journal Abstract Search

124 related items for PubMed ID: 1192826

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  • 6. Different gene mutations in variants of GM1- and GM2-gangliosidosis demonstrated by enzyme analysis of (single) somatic hybrid cells.
    Galjaard H, Hoogeveen A, Keijzer W, de Wit-Verbeek HA, Reuser AJ.
    Cytogenet Cell Genet; 1975; 14(3-6):320-6. PubMed ID: 1192809
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  • 7. Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis.
    Rattazzi MC, Brown JA, Davidson RG, Shows TB.
    Am J Hum Genet; 1976 Mar; 28(2):143-54. PubMed ID: 817596
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  • 8. Genetic variants of hexosaminidase deficiency.
    Patrick AD.
    Prog Clin Biol Res; 1977 Mar; 18():147-59. PubMed ID: 414238
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  • 10. [Genetic study of GM2 gangliosidosis (Tay-Sachs and Sandhoff) by the study of the hexosaminidases of the Sandhoff-rodents hybrids (mouse and hamster)].
    Weil D, Van Cong N, Rebourcet R, Frézal J.
    Ann Genet; 1975 Sep; 18(3):163-8. PubMed ID: 810067
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  • 12. Steroid hexosaminidase activity in Tay-Sachs and Sandhoff-Jatzkewitz diseases.
    Tomasi LG, Fukushima DK, Kolodny EH.
    Neurology; 1974 Dec; 24(12):1158-65. PubMed ID: 4280528
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  • 14. Juvenile Sandhoff Disease: complementation tests with Sandhoff and Tay-Sachs disease using polyethylene glycol-induced cell fusion.
    Wood S.
    Hum Genet; 1978 Apr 24; 41(3):325-9. PubMed ID: 417993
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  • 15. [Genetic complementation in the study of mechanisms of inborn errors of metabolism in man (review of the literature)].
    Baskaeva EM.
    Vopr Med Khim; 1990 Apr 24; 36(1):13-8. PubMed ID: 2188424
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  • 17. Serum hexosaminidase activity in I-cell disease carriers.
    Vidgoff J, Buist NR.
    Hum Genet; 1977 May 10; 36(3):307-16. PubMed ID: 852874
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  • 19. Current concepts in genetics. Lysosomal storage diseases.
    Kolodny EH.
    N Engl J Med; 1976 May 27; 294(22):1217-20. PubMed ID: 817200
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  • 20. Tay-Sachs' and Sandhoff's diseases: the assignment of genes for hexosaminidase A and B to individual human chromosomes.
    Gilbert F, Kucherlapati R, Creagan RP, Murnane MJ, Darlington GJ, Ruddle FH.
    Proc Natl Acad Sci U S A; 1975 Jan 27; 72(1):263-7. PubMed ID: 1054503
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