Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study

Overview of attention for article published in Orphanet Journal of Rare Diseases, April 2016

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Citations

dimensions_citation: 25 Dimensions

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mendeley: 33 Mendeley

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So far, Dimensions has found 25 publications that cite this research output.

25

The most recent citing publications are shown below. View all 25 publications that cite this research output on Dimensions.

Clinical Characteristics and Quality of Life in a Cohort of Polish Pediatric Patients with Hereditary Angioedema

Article in Children (February 2024)

Current challenges and future opportunities in patient‐focused management of hereditary angioedema: A narrative review

Article in Clinical and Translational Allergy (May 2023)

High digit ratio (2D:4D) is associated with attack frequency and severity in hereditary angioedema patients

Article in Early Human Development (February 2023)

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