Cargando…
Presence of C1-Inhibitor Polymers in a Subset of Patients Suffering from Hereditary Angioedema
Hereditary angioedema (HAE) is a potentially life-threatening disease caused by mutations in the gene encoding the serine protease inhibitor (serpin) C1 inhibitor (C1-inh). The mutations cause decreased functional plasma levels of C1-inh, which triggers unpredictable recurrent edema attacks. Subject...
Autores principales: | Madsen, Daniel Elenius, Hansen, Søren, Gram, Jørgen, Bygum, Anette, Drouet, Christian, Sidelmann, Johannes Jakobsen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219832/ https://www.ncbi.nlm.nih.gov/pubmed/25369003 http://dx.doi.org/10.1371/journal.pone.0112051 |
Ejemplares similares
-
Idiopathic Thrombocytopenic Purpura Misdiagnosed as Hereditary Angioedema
por: Andersen, Michelle Fog, et al.
Publicado: (2015) -
Socioeconomic burden of hereditary angioedema: results from the hereditary angioedema burden of illness study in Europe
por: Aygören-Pürsün, Emel, et al.
Publicado: (2014) -
Clinical characteristics and real-life diagnostic approaches in all Danish children with hereditary angioedema
por: Aabom, Anne, et al.
Publicado: (2017) -
Disease Severity, Activity, Impact, and Control and How to Assess Them in Patients with Hereditary Angioedema
por: Bygum, Anette, et al.
Publicado: (2017) -
Estimation of EuroQol 5-Dimensions health status utility values in hereditary angioedema
por: Aygören-Pürsün, Emel, et al.
Publicado: (2016)