Cargando…
Hypersensitivity reactions amongst Hungarian Patients with Hereditary Angioedema due to C1-Inhibitor Deficiency
BACKGROUND: In hereditary angioedema (HAE) due to C1-inhibitor deficiency (C1-INH-HAE), bradykinin-mediated submucosal and/or subcutaneous angioedema dominates the clinical picture. The deficiency of C1-inhibitor can lead to the over-activation of the complement system. Complement plays an important...
Autores principales: | Horváth, Hanga Réka, Szilágyi, Dávid, Andrási, Noémi, Balla, Zsuzsanna, Visy, Beáta, Farkas, Henriette |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
World Allergy Organization
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10618765/ https://www.ncbi.nlm.nih.gov/pubmed/37920275 http://dx.doi.org/10.1016/j.waojou.2023.100833 |
Ejemplares similares
-
Diagnosing Pediatric Patients With Hereditary C1-Inhibitor Deficiency—Experience From the Hungarian Angioedema Center of Reference and Excellence
por: Andrási, Noémi, et al.
Publicado: (2022) -
The analysis of the effect of the COVID-19 pandemic on patients with hereditary angioedema type I and type II
por: Szilágyi, Dávid, et al.
Publicado: (2023) -
Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema
por: Szabó, Edina, et al.
Publicado: (2022) -
The characteristics of upper airway edema in hereditary and acquired angioedema with C1‐inhibitor deficiency
por: Balla, Zsuzsanna, et al.
Publicado: (2021) -
Application of a dried blood spot based proteomic and genetic assay for diagnosing hereditary angioedema
por: Iuraşcu, Marius‐Ionuţ, et al.
Publicado: (2023)