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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 66 (1985), S. 78-82 
    ISSN: 1432-0533
    Keywords: Pallidal atrophy ; Corpus Luysii ; Amyotrophic lateral sclerosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The clinical and pathologic findings in a 34-year-old woman with basal ganglia degeneration and amyotrophic lateral sclerosis are reported. The duration of symptoms was 2 years. A maternal uncle had a parkinsonian syndrome with onset at 45 years of age. Neuropathologic examination revealed extensive neuronal loss and gliosis in the corpus Luysii. Nerve cell loss and gliosis also involved both parts of the globus pallidus, and the substantia nigra. The corticospinal tracts were demyelinated in the spinal cord, and neuronal loss was observed in the anterior horns. Only one similar case of pallido-luyso-nigral atrophy associated with amyotrophic lateral sclerosis has, to our knowledge, been reported previously. Such an association may represent more than a coincidental occurrence.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 25 (1973), S. 259-270 
    ISSN: 1432-0533
    Keywords: Tuberous Sclerosis ; Electron Microscopy ; Cerebral Biopsy ; Astrocytes ; Cerebral Tumor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The electron microscopic study of a cortical biopsy from a child presenting a Tuberous Sclerosis shows the importance of the astrocytic gliosis, the existence of abnormal cells of which two types can be recognized, and the presence of giant cells. All these cells are remarkable by the abundance of the ergastoplasm, the development of the Golgi apparatus, and the presence of membrane bound dense bodies. These cells are undoubtedly of astrocytic origin and appear very similar to the cells observed in a tumour of the caudate nucleus of another child affected by the same disease. These morphological data lead to believe that the cerebral abnormalities of the Tuberous Sclerosis essentially concern the astrocytes. The main characteristic of this astrocytic lesion would be its blastomatous potentiality.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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