Cargando…
Plasma Prekallikrein: Its Role in Hereditary Angioedema and Health and Disease
Plasma prekallikrein (PK) has a critical role in acute attacks of hereditary angioedema (HAE). Unlike C1 inhibitor, its levels fall during HAE attacks with resultant cleaved high-molecular-weight kininogen. Cleavage of high-molecular-weight kininogen liberates bradykinin, the major biologic peptide...
Autor principal: | Schmaier, Alvin H. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788901/ https://www.ncbi.nlm.nih.gov/pubmed/29423395 http://dx.doi.org/10.3389/fmed.2018.00003 |
Ejemplares similares
-
Lisinopril-Induced Angioedema in a Patient with Plasma Prekallikrein Deficiency
por: Dasgupta, Swapan K., et al.
Publicado: (2020) -
Hereditary Angioedema
por: Banerjee, Anjali, et al.
Publicado: (2023) -
The Search for Biomarkers in Hereditary Angioedema
por: Kaplan, Allen P., et al.
Publicado: (2017) -
Hereditary Angioedema: The Economics of Treatment of an Orphan Disease
por: Lumry, William Raymond
Publicado: (2018) -
Diagnostic Pearls and Clinical Implications of Prekallikrein Deficiency
por: Yasin, Hassaan, et al.
Publicado: (2020)