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Diagnosing Pediatric Patients With Hereditary C1-Inhibitor Deficiency—Experience From the Hungarian Angioedema Center of Reference and Excellence

Overview of attention for article published in Frontiers in Allergy, May 2022
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Title
Diagnosing Pediatric Patients With Hereditary C1-Inhibitor Deficiency—Experience From the Hungarian Angioedema Center of Reference and Excellence
Published in
Frontiers in Allergy, May 2022
DOI 10.3389/falgy.2022.860355
Pubmed ID
Authors

Noémi Andrási, Zsuzsanna Balla, Beáta Visy, Ágnes Szilágyi, Dorottya Csuka, Lilian Varga, Henriette Farkas

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 5 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 5 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 20%
Professor > Associate Professor 1 20%
Student > Bachelor 1 20%
Student > Postgraduate 1 20%
Unknown 1 20%
Readers by discipline Count As %
Medicine and Dentistry 2 40%
Pharmacology, Toxicology and Pharmaceutical Science 1 20%
Unknown 2 40%