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Hereditary angioedema with C1 inhibitor (C1-INH) deficit: the strength of recognition (51 cases)

Overview of attention for article published in Brazilian Journal of Medical and Biological Research, January 2018
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Title
Hereditary angioedema with C1 inhibitor (C1-INH) deficit: the strength of recognition (51 cases)
Published in
Brazilian Journal of Medical and Biological Research, January 2018
DOI 10.1590/1414-431x20187813
Pubmed ID
Authors

N.T.M.L. Fragnan, A.L.N. Tolentino, G.B. Borba, A.C. Oliveira, J.A. Simões, S.M.U. Palma, R.N. Constantino-Silva, A.S. Grumach

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 57 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 57 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 10 18%
Other 3 5%
Student > Postgraduate 3 5%
Researcher 3 5%
Student > Master 2 4%
Other 5 9%
Unknown 31 54%
Readers by discipline Count As %
Medicine and Dentistry 14 25%
Nursing and Health Professions 3 5%
Biochemistry, Genetics and Molecular Biology 2 4%
Psychology 2 4%
Business, Management and Accounting 1 2%
Other 4 7%
Unknown 31 54%