Picomolar Sensitivity Analysis of Multiple Bradykinin-Related Peptides in the Blood Plasma of Patients With Hereditary Angioedema in Remission: A Pilot Study

BACKGROUND: Hereditary angioedema (HAE) is a rare autosomal dominant disease; the most well understood forms concern the haplodeficiency of C1 esterase inhibitor (C1INH) and a gain of function mutation of factor XII (FXII). The acute forms of these conditions are mediated by an excessive bradykinin...

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Detalles Bibliográficos
Autores principales: Marceau, François, Rivard, Georges-Etienne, Hébert, Jacques, Gauthier, Julie, Bachelard, Hélène, Gangnus, Tanja, Burckhardt, Bjoern B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Allergy
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8974669/
https://www.ncbi.nlm.nih.gov/pubmed/35386662
http://dx.doi.org/10.3389/falgy.2022.837463

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8974669/
https://www.ncbi.nlm.nih.gov/pubmed/35386662
http://dx.doi.org/10.3389/falgy.2022.837463

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