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  • 1980-1984  (2)
  • Hepatosplenomegaly  (1)
  • Tay-Sachs disease  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Retinal amacrine cell involvement in Tay-Sachs disease (1981)
    Springer
    Acta neuropathologica 53 (1981), S. 333-336 
    Details
    ISSN: 1432-0533
    Keywords: Amacrine cell ; Tay-Sachs disease ; Ultrastructure ; Biochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Ultrastructural study of the retina from a patient with Tay-Sachs disease disclosed that amacrine cells as well as ganglion cells were loaded with numerous membranous cytoplasmic bodies, suggesting an accumulation of GM2 ganglioside, whereas the horizontal cells, bipolar cells, and photoreceptor cells were intact. Chromatography of lipids from the retina showed a prominent spot of GM2 ganglioside. These facts suggest that lipid metabolism in amacrine cells may be different from that in other retinal cells.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00690376
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Chronic recurrent demyelinating encephalomyelitis associated with hemophagocytic lymphohistiocytosis (1983)
    Springer
    Acta neuropathologica 59 (1983), S. 25-30 
    Details
    ISSN: 1432-0533
    Keywords: Demyelinating disease ; Infundibulo-hypophysitis ; Hepatosplenomegaly ; Hemophagocytic lymphohistiocytosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A man aged 31 with remittent fever, leukopenia, polyuria, and splenomegaly in addition to chronic and recurrent episodes of neurologic abnormalities was examined pathologically. A chronic type of perivenous encephalomyelitis was found in the CNS, and chronic inflammatory lesions were noticed in the infundibulo-hypophyseal system and also in the peripheral nerves. Moreover, hemophagocytic lymphohistiocytosis predominated in the reticuloendothelial system. This seemed to be the first adult case of demyelinating disease with hemophagocytic lymphohistiocytosis.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00690313
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
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