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Miglustat therapy in the French cohort of paediatric patients with Niemann-Pick disease type C

Overview of attention for article published in Orphanet Journal of Rare Diseases, June 2012
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Citations

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Title
Miglustat therapy in the French cohort of paediatric patients with Niemann-Pick disease type C
Published in
Orphanet Journal of Rare Diseases, June 2012
DOI 10.1186/1750-1172-7-36
Pubmed ID
Authors

Bénédicte Héron, Vassili Valayannopoulos, Julien Baruteau, Brigitte Chabrol, Hélène Ogier, Philippe Latour, Dries Dobbelaere, Didier Eyer, François Labarthe, Hélène Maurey, Jean-Marie Cuisset, Thierry Billette de Villemeur, Frédéric Sedel, Marie T Vanier

Abstract

Niemann-Pick disease type C (NP-C) is a rare neurovisceral lysosomal lipid storage disease characterized by progressive neurological deterioration. Published data on the use of miglustat in paediatric patients in clinical practice settings are limited. We report findings from a prospective open-label study in the French paediatric NP-C cohort.

X Demographics

X Demographics

The data shown below were collected from the profiles of 3 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 113 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Russia 1 <1%
Germany 1 <1%
Unknown 111 98%

Demographic breakdown

Readers by professional status Count As %
Researcher 20 18%
Student > Bachelor 13 12%
Student > Ph. D. Student 11 10%
Other 10 9%
Student > Master 9 8%
Other 23 20%
Unknown 27 24%
Readers by discipline Count As %
Medicine and Dentistry 37 33%
Biochemistry, Genetics and Molecular Biology 13 12%
Agricultural and Biological Sciences 10 9%
Neuroscience 7 6%
Nursing and Health Professions 5 4%
Other 9 8%
Unknown 32 28%
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 01 September 2012.
All research outputs
#13,363,429
of 22,668,244 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,378
of 2,594 outputs
Outputs of similar age
#92,627
of 166,837 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#8
of 15 outputs
Altmetric has tracked 22,668,244 research outputs across all sources so far. This one is in the 39th percentile – i.e., 39% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,594 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 7.4. This one is in the 44th percentile – i.e., 44% 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 166,837 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 42nd percentile – i.e., 42% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 15 others from the same source and published within six weeks on either side of this one. This one is in the 26th percentile – i.e., 26% of its contemporaries scored the same or lower than it.