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Mendeley readers
| Title |
Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence
|
|---|---|
| Published in |
Orphanet Journal of Rare Diseases, October 2020
|
| DOI | 10.1186/s13023-020-01570-x |
| Pubmed ID | |
| Authors |
Konrad Bork, Thomas Machnig, Karin Wulff, Guenther Witzke, Subhransu Prusty, Jochen Hardt |
Mendeley readers
The data shown below were compiled from readership statistics for 70 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 70 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Researcher | 8 | 11% |
| Other | 7 | 10% |
| Student > Master | 7 | 10% |
| Student > Bachelor | 6 | 9% |
| Student > Ph. D. Student | 4 | 6% |
| Other | 5 | 7% |
| Unknown | 33 | 47% |
| Readers by discipline | Count | As % |
|---|---|---|
| Medicine and Dentistry | 22 | 31% |
| Biochemistry, Genetics and Molecular Biology | 2 | 3% |
| Immunology and Microbiology | 2 | 3% |
| Nursing and Health Professions | 2 | 3% |
| Pharmacology, Toxicology and Pharmaceutical Science | 1 | 1% |
| Other | 7 | 10% |
| Unknown | 34 | 49% |