You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output.
Click here to find out more.
Mendeley readers
| Title |
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG
|
|---|---|
| Published in |
BMC Neurology, August 2020
|
| DOI | 10.1186/s12883-020-01890-2 |
| Pubmed ID | |
| Authors |
Davide Villa, Claudia Cinnante, Gloria Valcamonica, Giulia Manenti, Silvia Lanfranconi, Annalisa Colombi, Isabella Ghione, Maria Cristina Saetti, Mario D’Amico, Sara Bonato, Nereo Bresolin, Giacomo Pietro Comi, Dario Ronchi |
Mendeley readers
The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 15 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Master | 3 | 20% |
| Student > Bachelor | 3 | 20% |
| Student > Doctoral Student | 2 | 13% |
| Unspecified | 1 | 7% |
| Researcher | 1 | 7% |
| Other | 0 | 0% |
| Unknown | 5 | 33% |
| Readers by discipline | Count | As % |
|---|---|---|
| Medicine and Dentistry | 4 | 27% |
| Neuroscience | 3 | 20% |
| Unspecified | 1 | 7% |
| Nursing and Health Professions | 1 | 7% |
| Unknown | 6 | 40% |