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  • 1
    Electronic Resource
    Electronic Resource
    Ultrastructural study of three cases of encephalopathy with hypsarrhythmia (1982)
    Springer
    Acta neuropathologica 56 (1982), S. 311-314 
    Details
    ISSN: 1432-0533
    Keywords: Encephalopathy with hypsarrhythmia ; Spongiform changes of cerebral cortex ; Cell fusion index
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We report a morphological study of three cases of infantile hypsarrhythmia. The cerebral cortex lesions consisted of a diffuse neuropile microspongiosis, corresponding ultrastructurally to vacuolized and enlarged neuronal processes, particularly postsynaptic bags. The morphological aspects and the high cell fusion index in one case resemble those described in transmissible subacute spongiform encephalopathies.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00691265
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Étude clinique, histologique et ultrastructurale de quatre cas de leucodystrophie métachromatique infantile et juvénile (1972)
    Springer
    Acta neuropathologica 21 (1972), S. 23-38 
    Details
    ISSN: 1432-0533
    Keywords: Leucodystrophy Metachromatic ; Electron Microscopy ; Prismatic Deposits ; Brain ; Peripheral Nerve ; Kidney ; Rectum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Clinical history, light and electron microscopy findings are reported in four cases of infantile metachromatic leucodystrophy. By electron microscopy, the authors describe the various types of lesions and the different lipid deposits noticed in the central and peripheral nervous system, in the kidney and rectum. They stress the prismatic lipid deposits observed not only in the cerebral white matter and in the kidney but in the peripheral nerves as well.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00687997
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    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Céroïde-lipofuscinose neuronale (1974)
    Springer
    Acta neuropathologica 28 (1974), S. 353-359 
    Details
    ISSN: 1432-0533
    Keywords: Familial Céroïd-Lipofuscinosis ; Batten Disease ; Late Infantile Amaurotic Idiocy ; Consanguinity ; Curvilmear, Finger-Print Inclusions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The authors report histochemical and electron mciroscopic data of brain biopsies in two cases of Battern's disease. The siblings affected, a male and a female, are born from consanguineous North African parents. The diagnosis of Ceroïd-Lipofuscinosis is supported by neuro-glial, endothelial and perithelial autofluorescent cell storage. By electron microscopy the abnormal cytosomes show both curvilinear and finger-print profiles; their lysosomal nature is supported by their obvious acid phosphatase activity. These lipopigment cytoplasmic inclusions are compared with those described in senile brains and in other cases of Batten's disease.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00685289
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    Paper (German National Licenses)
    Fulltext
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