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Quality of life in patients with Fabry disease: a systematic review of the literature

Overview of attention for article published in Orphanet Journal of Rare Diseases, June 2015
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  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (83rd percentile)
  • Good Attention Score compared to outputs of the same age and source (77th percentile)

Mentioned by

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1 policy source
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10 X users
facebook
1 Facebook page

Citations

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75 Dimensions

Readers on

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94 Mendeley
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Title
Quality of life in patients with Fabry disease: a systematic review of the literature
Published in
Orphanet Journal of Rare Diseases, June 2015
DOI 10.1186/s13023-015-0296-8
Pubmed ID
Authors

Maarten Arends, Carla E. M. Hollak, Marieke Biegstraaten

Abstract

Fabry disease (FD), caused by deficiency of the lysosomal enzyme α-galactosidase-A, is a progressive multisystem disease. The disease is X-linked with generally more severe manifestations in males, but can impact on quality of life (QoL) of both male and female patients. The purpose of this literature review is to analyse the currently available data concerning QoL measurement, specifically which questionnaires have been used to measure QoL, how patients with FD score compared to the general population, and the effects of enzyme replacement therapy (ERT) on QoL. Fifty-four articles were relevant for this literature review. Patients with FD had a lower QoL compared to the general population. No definite conclusions could be drawn from the studies on the effect of ERT on QoL; natural history data is scarce, changes observed were limited and the cohorts were of small size. We propose that a FD specific questionnaire be made to accurately assess QoL in patients with FD.

X Demographics

X Demographics

The data shown below were collected from the profiles of 10 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 94 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
France 1 1%
Unknown 93 99%

Demographic breakdown

Readers by professional status Count As %
Student > Master 17 18%
Researcher 11 12%
Student > Ph. D. Student 11 12%
Student > Bachelor 11 12%
Student > Doctoral Student 5 5%
Other 12 13%
Unknown 27 29%
Readers by discipline Count As %
Medicine and Dentistry 30 32%
Agricultural and Biological Sciences 7 7%
Biochemistry, Genetics and Molecular Biology 5 5%
Pharmacology, Toxicology and Pharmaceutical Science 5 5%
Nursing and Health Professions 4 4%
Other 16 17%
Unknown 27 29%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 10. 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 February 2018.
All research outputs
#3,713,533
of 25,595,500 outputs
Outputs from Orphanet Journal of Rare Diseases
#546
of 3,155 outputs
Outputs of similar age
#43,475
of 264,420 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#10
of 40 outputs
Altmetric has tracked 25,595,500 research outputs across all sources so far. Compared to these this one has done well and is in the 85th percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 3,155 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 8.2. This one has done well, scoring higher than 82% 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 264,420 tracked outputs that were published within six weeks on either side of this one in any source. This one has done well, scoring higher than 83% of its contemporaries.
We're also able to compare this research output to 40 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 77% of its contemporaries.