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  • 1
    Electronic Resource
    Electronic Resource
    Encephalomyeloneuropathy in the absence of a detectable neoplasm (1985)
    Springer
    Acta neuropathologica 66 (1985), S. 311-317 
    Details
    ISSN: 1432-0533
    Keywords: Encephalomyeloneuropathy ; Sensory neuropathy ; Brain stem encephalitis ; Limbic encephalitis ; Ganglioradiculitis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The clinical and postmortem findings in three cases of encephalomyeloneuropathy are reported. Two patients presented with subacute sensory neuropathy and one with amnesia and confusion. In none of these cases was a tumour detected clinically or at autopsy. Neuropathological examination showed inflammatory lesions in the brain, spinal cord and posterior root ganglia indistinguishable from encephalomyeloneuropathy occurring as a remote effect of carcinoma.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00690964
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies (1988)
    [s.l.] : Nature Publishing Group
    Nature 331 (1988), S. 717-719 
    Details
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The term mitochondrial myopathy (MM) describes a heterogeneous group of disorders which share the common feature of major structural mitochondrial abnormalities in skeletal muscle. The clinical features are variable and include proximal muscle weakness, external ophthalmoplegia, pigmentary ...
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1038/331717a0
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Mitochondrial DNA polymorphism in mitochondrial myopathy (1988)
    Springer
    Human genetics 〈Berlin〉 79 (1988), S. 53-57 
    Details
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary In order to test the hypothesis that mitochondrial myopathy may be caused by mutation of the mitochondrial (mt) genome, restriction fragment length polymorphism in leucocyte mt DNA has been studied in 38 patients with mitochondrial myopathy, 44 of their unaffected matrilineal relatives, and 35 normal control subjects. Previously unreported mt DNA polymorphisms were identified in both patients and controls. No differences in restriction fragment patterns were observed between affected and unaffected individuals in the same maternal line, and there was no evidence of major deletion of mt DNA in patients. This study provides no positive evidence of mitochondrial inheritance in mitochondrial myopathy, but this has not been excluded.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00291710
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    Paper (German National Licenses)
    Fulltext
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