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Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP)

Overview of attention for article published in Orphanet Journal of Rare Diseases, October 2013
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1 X user
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1 Google+ user

Citations

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47 Mendeley
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Title
Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP)
Published in
Orphanet Journal of Rare Diseases, October 2013
DOI 10.1186/1750-1172-8-158
Pubmed ID
Authors

Kathrin N Karle, Rebecca Schüle, Stephan Klebe, Susanne Otto, Christian Frischholz, Inga Liepelt-Scarfone, Ludger Schöls

Abstract

Hereditary spastic paraplegias (HSPs) are characterised by lower limb spasticity due to degeneration of the corticospinal tract. We set out for an electrophysiological characterisation of motor and sensory tracts in patients with HSP.

X Demographics

X Demographics

The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 47 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 47 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 14 30%
Student > Postgraduate 6 13%
Student > Master 4 9%
Researcher 4 9%
Student > Ph. D. Student 4 9%
Other 8 17%
Unknown 7 15%
Readers by discipline Count As %
Medicine and Dentistry 16 34%
Nursing and Health Professions 6 13%
Neuroscience 6 13%
Agricultural and Biological Sciences 4 9%
Biochemistry, Genetics and Molecular Biology 4 9%
Other 4 9%
Unknown 7 15%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 10 October 2013.
All research outputs
#14,178,787
of 22,725,280 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,553
of 2,604 outputs
Outputs of similar age
#117,597
of 209,651 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#24
of 33 outputs
Altmetric has tracked 22,725,280 research outputs across all sources so far. This one is in the 35th percentile – i.e., 35% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,604 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.5. This one is in the 36th percentile – i.e., 36% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 209,651 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 41st percentile – i.e., 41% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 33 others from the same source and published within six weeks on either side of this one. This one is in the 24th percentile – i.e., 24% of its contemporaries scored the same or lower than it.