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  • 1975-1979  (3)
  • Brain tumor  (1)
  • Electron microscope  (1)
  • Incomplete innervation  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Virchows Archiv 375 (1977), S. 13-22 
    ISSN: 1432-2307
    Keywords: Target-targetoid phenomenon ; Histochemistry ; Electron microscopy ; Z-band alteration ; Incomplete innervation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Target and targetoid fibers in a muscle biopsy from a patient with paralysis of the deltoid and supraspinatus muscles were studied by light and electron microscopy. The probable cause of the neuropathy was tumor compression. Target and targetoid change was exclusively confined to hypertrophic or normal-sized fibers. Morphometric evaluation of the target and targetoid fibers showed no significant difference between them. With the electron microscope, up to 4 structural zones were seen in the typical target fiber but many were devoid of either zone 2 (halo) or zone 3, or both. It was conceivable that focal irregularity and streaming of Z-bands were the primary alterations in the process of target-targetoid fiber formation, and that this phenomenon was induced both by partial residual innervation as well as re-innervation.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 41 (1978), S. 257-259 
    ISSN: 1432-0533
    Keywords: Infantile neuroaxonal dystrophy ; Sural nerve biopsy ; Electron microscope ; Schwann cell inclusions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Abnormal Schwann cell inclusion is reported in biopsied peripheral nerve in a cases of infantile neuroaxonal dystrophy. In addition to non-specific dystrophic changes of the axons, the Schwann cells contained several distinct bodies which were composed of stacks of irregularly disposed membranes; in some instances, transformed Schwann cell cytoplasm was distinded with similar bodies. This change has not been reported on this condition and its significance is briefly discussed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 45 (1979), S. 111-115 
    ISSN: 1432-0533
    Keywords: Brain tumor ; Rhabdomyosarcoma ; Mesenchymal cell ; Myotube ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A case of primary cerebral rhabdomyosarcoma in a 51-year-old female is reported. The histogenesis of this tumor is discussed. The clinicopathological features of 10 previously reported similar tumors of the CNS are briefly reviewed. Histologically the tumor was polymorphic, but composed of poorly differentiated cells interpreted as rhabdomyoblasts without definite cross-striation. Electron microscopy established that the poorly differentiated cells were of rhabdomyosarcomatous nature, compatible with presumptive myoblasts and analogous to developing fetal muscle.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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