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Journal Abstract Search

136 related items for PubMed ID: 607830

  • 1. [GM2 gangliosidosis diagnosis and carriers detection by fractionation of N-acetyl-beta-D-hexosaminidase by electrophoresis on cellulose acetate gel (author's transl)].
    Pampols T, Girós ML, González Sastre F, Sabater J.
    An Esp Pediatr; 1977 Oct; 10(10):695-704. PubMed ID: 607830
    [Abstract] [Full Text] [Related]

  • 2. [Prenatal biochemical diagnosis of Tay-Sachs disease].
    Rozenfel'd EL, Tsvetkova IV, Kozina AB, Rozovskiĭ IS, Kovrigina NG.
    Vopr Med Khim; 1972 Oct; 18(4):445-6. PubMed ID: 4661856
    [No Abstract] [Full Text] [Related]

  • 3. [Prenatal diagnosis of Sandhoff's disease (GM2-gangliosidosis, type 2)].
    Harzer K, Stengel-Rutkowski S, Gley EO, Albert A, Murken JD, Zahn V, Henkel KP.
    Dtsch Med Wochenschr; 1975 Jan 17; 100(3):106-8. PubMed ID: 234374
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  • 4. The prenatal diagnosis of Tay-Sachs disease.
    Lane AB, Skikne MI, Jenkins T.
    S Afr Med J; 1976 Sep 18; 50(40):1553-5. PubMed ID: 982208
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  • 5. Rapid detection of fetal Mendelian disorders: Tay-Sachs disease.
    Guetta E, Peleg L.
    Methods Mol Biol; 2008 Sep 18; 444():147-59. PubMed ID: 18425478
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  • 6. Human hexosaminidase isozymes: chromatographic separation as an aid to heterozygote identification.
    Nakagawa S, Kumin S, Nitowsky HM.
    Clin Chim Acta; 1977 Mar 01; 75(2):181-91. PubMed ID: 851488
    [Abstract] [Full Text] [Related]

  • 7. Hexosaminidase A in amniotic fluid of Tay-Sachs fetuses.
    Geiger B, Navon R, Arnon R.
    Clin Chem; 1978 Jul 01; 24(7):1131-3. PubMed ID: 657491
    [Abstract] [Full Text] [Related]

  • 8. [Prenatal genetic diagnosis in a family with Tay-Sachs disease (enzyme variant B) (author's transl)].
    Pilz H, Linke I, Käckell MY, Haller J, Lenard HG.
    Dtsch Med Wochenschr; 1974 Mar 22; 99(12):578-80. PubMed ID: 4835528
    [No Abstract] [Full Text] [Related]

  • 9. [Preliminary results in the prenatal diagnosis of Tay-Sachs disease by isoelectric focusing of hexosaminidase A (author's transl)].
    Harzer K.
    Klin Wochenschr; 1974 Feb 01; 52(3):145-7. PubMed ID: 4826655
    [No Abstract] [Full Text] [Related]

  • 10. Prenatal diagnosis and fetal pathology of Tay-Sachs disease.
    Higami S, Nishizawa K, Omura K, Sugimoto K, Isshiki G.
    Tohoku J Exp Med; 1976 Apr 01; 118(4):323-30. PubMed ID: 936207
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  • 13. Prenatal diagnosis of Tay-Sachs genotypes.
    Navon R, Padeh B.
    Br Med J; 1971 Oct 02; 4(5778):17-20. PubMed ID: 5096878
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  • 15. Diagnosis of Tay-Sachs disease by hexosaminidase activity in leukocytes and amniotic fluid cells.
    Padeh B, Navon R.
    Isr J Med Sci; 1971 Feb 02; 7(2):259-63. PubMed ID: 5560980
    [No Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of Tay-Sachs disease with heat-labile beta-hexosaminidase B.
    Momoi T, Kikuchi K, Shigematsu Y, Sudo M, Tanioka K.
    Clin Chim Acta; 1983 Oct 14; 133(3):331-4. PubMed ID: 6226459
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  • 17. [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 14; 18(3):163-8. PubMed ID: 810067
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