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Natural history of Sanfilippo syndrome in Spain

Overview of attention for article published in Orphanet Journal of Rare Diseases, December 2013
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (92nd percentile)
  • High Attention Score compared to outputs of the same age and source (89th percentile)

Mentioned by

blogs
1 blog
twitter
11 X users
facebook
3 Facebook pages
googleplus
1 Google+ user

Citations

dimensions_citation
52 Dimensions

Readers on

mendeley
104 Mendeley
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Title
Natural history of Sanfilippo syndrome in Spain
Published in
Orphanet Journal of Rare Diseases, December 2013
DOI 10.1186/1750-1172-8-189
Pubmed ID
Authors

Verónica Delgadillo, Maria del Mar O’Callaghan, Laura Gort, Maria Josep Coll, Mercedes Pineda

Abstract

Mucopolysaccharidosis type III (MPS III), or Sanfilippo syndrome, is caused by a deficiency in one of the four enzymes involved in the lysosomal degradation of heparan sulphate. Four MPS III types have been recognized, characterized by a large phenotypic heterogeneity. This is the first Spanish study describing the natural history of Sanfilippo patients (MPSIIIA, MPSIIIB and MPSIIIC), representing an essential step for understanding patient prognosis and for the establishment and application of future therapies.

X Demographics

X Demographics

The data shown below were collected from the profiles of 11 X users 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 104 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Netherlands 1 <1%
Unknown 103 99%

Demographic breakdown

Readers by professional status Count As %
Researcher 19 18%
Student > Bachelor 14 13%
Student > Master 11 11%
Student > Ph. D. Student 10 10%
Other 9 9%
Other 16 15%
Unknown 25 24%
Readers by discipline Count As %
Medicine and Dentistry 25 24%
Biochemistry, Genetics and Molecular Biology 14 13%
Agricultural and Biological Sciences 14 13%
Psychology 7 7%
Neuroscience 6 6%
Other 13 13%
Unknown 25 24%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 16. 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 08 September 2018.
All research outputs
#2,262,624
of 25,373,627 outputs
Outputs from Orphanet Journal of Rare Diseases
#265
of 3,105 outputs
Outputs of similar age
#24,908
of 319,937 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#4
of 37 outputs
Altmetric has tracked 25,373,627 research outputs across all sources so far. Compared to these this one has done particularly well and is in the 91st percentile: it's in the top 10% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 3,105 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 8.2. This one has done particularly well, scoring higher than 91% of its peers.
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 319,937 tracked outputs that were published within six weeks on either side of this one in any source. This one has done particularly well, scoring higher than 92% of its contemporaries.
We're also able to compare this research output to 37 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 89% of its contemporaries.