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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 45 (1979), S. 133-140 
    ISSN: 1432-0533
    Keywords: Alexander's disease ; Rosenthal's fibers ; Peripheral Nerve ; Electron microscopy ; Neurochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The authors report the results of a cerebral and of a neuromuscular biopsies and of the autopsy findings in another infantile case of Alexander's disease in a girl. They review the 17 previously reported cases of this disease and the various etiopathogenic hypotheses mentioned. The presence of numerous, sometimes abnormal enlarged mitochondria and of abundant membranous cytoplasmic bodies in the astrocytic cytoplasm seems to be unreported elsewhere. Peripheral nerve changes are mentioned for the first time.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 37 (1977), S. 263-265 
    ISSN: 1432-0533
    Keywords: Progressive multifocal leukoencephalopathy ; Multiple sclerosis ; Demyelination ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Inclusions identical to those described in multiple sclerosis (MS) brain by Prineas (1975) have been seen by ultrastructural study of cerebral tissue in two elsewhere reported cases of Progressive Multifocal Leukoencephalopathy (PML). The meaning of these formations, which have been suggested to be related to a special process of demyelination in MS, is discussed in the light of the hypotheses concerning the demyelination mechanism in PML. Whatever might be their significance, these cytoplasmic non viral inclusions are not specific for MS.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-0533
    Keywords: Perexiline maleate ; Drug-induced neuropathy ; Nerve biopsy ; Muscle biopsy ; Skin biopsy ; Electron microscopy ; Lysosomes ; Segmental demyelination
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The pathological findings in four nerves and muscles and in one skin biopsies from four patients treated with perhexiline maleate for angina pectoris are reported. In every case, a muscular denervation atrophy and a decrease in the large diameter myelinated fibers were observed. Only one case showed a decrease of the total number of myelinated fibers, on quantitative studies. The electron microscopic study of each nerve displayed findings consistent with a predominant schwannian degeneration, associated with a few onion bulbs formations and, in two cases, with a mild wallerian degeneration. The most striking finding consisted in the presence of polymorphous membrane-bound inclusions reminding the morphology of lysosomal complex lipids. These structures were very abundant in Schwann cells, but they were seen also in fibrocytes, endothelial and pericytic cells. Similar inclusions were present in the single muscle and skin biopsies studied by electron microscopy. In the muscle, they were seen in muscular cells as well as in endothelial and pericytic cells. In the skin, similar inclusions were observed in endothelial, smooth muscle and sweat gland cells. These inclusions were difficult to identifiy in one micron thick sections, emphazing the need of ultrastructural study for diagnostic purposes.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0533
    Keywords: Sensory neuropathy ; Nerve biopsy ; Electron microscopy ; Quantitative study
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary An electron microscope study and quantitation of myelinated and unmyelinated fibers of seven nerve biopsies performed in sporadic cases of idiopathic sensory neuropathy is reported. The number of myelinated fibers is markedly decreased or absent in every case. On the contrary, the unmyelinated fiber numbers are normal or increased. In most cases, the small diameter myelinated and unmyelinated fibers proportions are higher than those of control biopsies. The electron microscope study discloses evidence of degeneration of Wallerian type and regeneration is also indicated by quantitative studies. Regenerative phenomena seem more obvious in sporadic cases than in previously reported studies of familial cases.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 10 (1968), S. 279-294 
    ISSN: 1432-0533
    Keywords: Neurofibromas ; von Recklinghausen's disease ; Neurinomas (or schwannomas) ; Electron microscopy ; Peripheral nervous tumors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Résumé L'examen en microscopie optique et électronique de 6 neurofibromes prélevés chirurgicalement chez des patients atteints de maladie de Recklinghausen autorise un certain nombre de conclusions: l'ultrastructure des neurofibromes est faite de 2 types de cellules (cellules de Schwann et fibroblastes) dispersées au sein d'un espace extra-cellulaire contenant de nombreuses fibres de collagène. Des axones myélinisés et amyéliniques sont présents; l'aspect ultrastructural de 3 neurinomes de l'acoustique a été comparé à celui des neurofibromes et apparaît comme différent. Les neurinomes sont faits d'un seul type cellulaire (très probablement cellule de Schwann), le collagène y est beaucoup moins abondant, les axones absents. Quelques déductions pathogéniques et nosologiques sont proposées.
    Notes: Summary Six neurofibromas from patients with von Recklinghausen's disease have been examined by light and electron microscopy: 2 types of cells have been found (Schwann cells and fibroblasts) scattered in extracellular spaces rich in collagen fibers. Myelinated and nonmyelinated axons were observed. These data have been compared with other ones collected from 3 acoustic neurinomas. These latter contained only one cellular type (very likely to be Schwann cell), much less collagen and no axon at all. A pathogenic and nosologic discussion is given.
    Type of Medium: Electronic Resource
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