Library

X
feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    An unusual case of lower motor neuron disease (1983)
    Springer
    Journal of neurology 230 (1983), S. 141-142 
    Details
    ISSN: 1432-1459
    Keywords: Lower motor neuron disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Ein Fall einer ungewöhnlichen Schädigung des peripheren Motorneurons wird beschrieben. Ein 11jähriger Junge litt an einer schnellverschlechternden unsymmetrischen Tetraparese mit tödlichem Ende nach einem Jahr. Die Klassifizierung dieses ungewöhnlichen Falles wird diskutiert.
    Notes: Summary An 11-year-old boy developed a rapidly progressive asymmetrical flaccid tetraparesis that ended fatally within 1 year. The classification of this unusual case is discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00313642
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    McArdle's disease: two clinical expressions in the same pedigree (1990)
    Springer
    Journal of neurology 237 (1990), S. 267-270 
    Details
    ISSN: 1432-1459
    Keywords: McArdle's disease ; Myoglobinuria ; Phosphorylase deficiency
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Two patients with McArdle's disease within the same pedigree and with two different clinical forms are presented. The first patient suffered from progressive muscle weakness and atrophy. Muscle morphology was that of myopathy. Residual activity of phosphorylase was 28% and sodium dodecyl sulphate electrophoresis showed decreased protein. The second case was typical of McArdle's disease, clinically and biochemically. It was concluded that the first patient was a heterozygote (residual activity 28% of normal) and the second was a homozygote, the genetic transmission being autosomal recessive.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00314633
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Nucleo-cytoplasmic ratio in ageing skeletal muscle (1987)
    Springer
    European archives of psychiatry and clinical neuroscience 236 (1987), S. 235-236 
    Details
    ISSN: 1433-8491
    Keywords: Ageing ; Skeletal muscle ; Karyometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In order to investigate possible changes in the nucleo-cytoplasmic ratio of the muscle fibres during ageing, samples of quadriceps femoris from 15 normal individuals whose age ranged from 17 to 82 years were studied (autopsy material). The mean lesser diameter and the number and size of the muscle fibre nuclei were calculated using a planimetric technique. It was found that nucleo-cytoplasmic ratio increased significantly after the age of 60 years. This was due to a decrease in the mean fibre size whilst the number and the size of myonuclei remained unchanged. The resemblance of this finding to denervation atrophy changes is noted.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00383854
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...