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Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures

Overview of attention for article published in Orphanet Journal of Rare Diseases, April 2020
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Citations

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63 Mendeley
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Title
Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures
Published in
Orphanet Journal of Rare Diseases, April 2020
DOI 10.1186/s13023-020-01353-4
Pubmed ID
Authors

P. Vanherpe, S. Fieuws, A. D’Hondt, C. Bleyenheuft, P. Demaerel, J. De Bleecker, P. Van den Bergh, J. Baets, G. Remiche, K. Verhoeven, S. Delstanche, M. Toussaint, B. Buyse, P. Van Damme, C. E. Depuydt, K. G. Claeys

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 63 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 63 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 7 11%
Student > Bachelor 6 10%
Student > Master 5 8%
Student > Ph. D. Student 4 6%
Student > Doctoral Student 3 5%
Other 5 8%
Unknown 33 52%
Readers by discipline Count As %
Medicine and Dentistry 11 17%
Biochemistry, Genetics and Molecular Biology 8 13%
Neuroscience 4 6%
Pharmacology, Toxicology and Pharmaceutical Science 1 2%
Nursing and Health Professions 1 2%
Other 3 5%
Unknown 35 56%