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Journal Abstract Search

80 related items for PubMed ID: 817606

  • 1.
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  • 2. Morphogenesis of light and electron microscopic lesions in porcine GM2-gangliosidosis.
    Kosanke SD, Pierce KR, Read WK.
    Vet Pathol; 1979 Jan; 16(1):6-17. PubMed ID: 111405
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  • 3. Clinical and biochemical abnormalities in porcine GM2-gangliosidosis.
    Kosanke SD, Pierce KR, Bay WW.
    Vet Pathol; 1978 Nov; 15(6):685-99. PubMed ID: 108843
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  • 5. AB variant GM2 gangliosidosis: cerebrospinal fluid and neuropathologic characteristics.
    Kotagal S, Wenger DA, Alcala H, Gomez C, Horenstein S.
    Neurology; 1986 Mar; 36(3):438-40. PubMed ID: 3081832
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  • 9. Antisera against ganglioside GM2: immunochemical and immunohistological studies.
    Schwerer B, Lassmann H, Bernheimer H.
    Neuropathol Appl Neurobiol; 1982 Mar; 8(3):217-26. PubMed ID: 6214725
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  • 11. Assay of ganglioside GM2-N-acetyl-beta-D-galactosaminidase activity in human fibroblasts employing the natural activator protein--diagnosis of variant forms of GM2 gangliosidosis.
    Erzberger A, Conzelmann E, Sandhoff K.
    Clin Chim Acta; 1980 Dec 22; 108(3):361-8. PubMed ID: 6781795
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  • 13. GM2 ganglioside lysosomal storage disease in cats with beta-hexosaminidase deficiency.
    Cork LC, Munnell JF, Lorenz MD, Murphy JV, Baker HJ, Rattazzi MC.
    Science; 1977 May 27; 196(4293):1014-7. PubMed ID: 404709
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  • 14. Diagnosis of infantile and juvenile forms of GM2 gangliosidosis variant 0. Residual activities toward natural and different synthetic substrates.
    Kytzia HJ, Hinrichs U, Sandhoff K.
    Hum Genet; 1984 May 27; 67(4):414-8. PubMed ID: 6436167
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  • 15. Lysosomal storage diseases in adults.
    Rapola J.
    Pathol Res Pract; 1994 Sep 27; 190(8):759-66. PubMed ID: 7831151
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  • 16. Animal model of human disease. GMi-gangliosidosis type II. Animal model: Bovine GMi-gangliosidosis, cerebrospinal lipidosis of Friesian cattle.
    Donnelly WJ, Sheahan BJ.
    Am J Pathol; 1975 Oct 27; 81(1):255-8. PubMed ID: 810033
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  • 17. 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.
    Birth Defects Orig Artic Ser; 1975 Oct 27; 11(3):150-6. PubMed ID: 812565
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  • 18. [Enzymes of glycolipid metabolism and their role in the development of glycolipidoses].
    Mkheian EE.
    Vestn Akad Med Nauk SSSR; 1983 Oct 27; (4):71-7. PubMed ID: 6306946
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  • 19. Hexosaminidase deficiency: a cause of recessively inherited motor neuron diseases.
    Johnson WG.
    Adv Neurol; 1982 Oct 27; 36():159-64. PubMed ID: 6817610
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  • 20. Brain hexosaminidase and arylsulfatase isoenzymes in normal and vitamin E-deficient rats: an hypothesis for isoenzyme patterns in GM2 gangliosidoses and MLD.
    Koenig H, Patel A.
    Trans Am Neurol Assoc; 1974 Oct 27; 99():140-3. PubMed ID: 4463525
    [No Abstract] [Full Text] [Related]

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