Thrombin in the Activation of the Fluid Contact Phase in Patients with Hereditary Angioedema Carrying the F12 P.Thr309Lys Variant-Reference-Cited by-同舟云学术

Thrombin in the Activation of the Fluid Contact Phase in Patients with Hereditary Angioedema Carrying the F12 P.Thr309Lys Variant

Published:2021-03-16 Issue:3 Volume:60 Page:357-368
ISSN:1080-0549
Container-title:Clinical Reviews in Allergy & Immunology
language:en
Short-container-title:Clinic Rev Allerg Immunol

Author:

López-Gálvez R.,de la Morena-Barrio M. E.,Miñano A.,Pathak M.,Marcos C.,Emsley J.,Caballero T.,López-Trascasa M.,Vicente V.,Corral J.,López-Lera A.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Immunology and Allergy

Link

https://link.springer.com/content/pdf/10.1007/s12016-021-08840-x.pdf

Reference31 articles.

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2. Maas C, López-Lera A (2019) Hereditary angioedema: insights into inflammation and allergy. Mol Immunol 112:378–386

3. Donaldson VH, Evans RR (1963) A biochemical abnormality in hereditary angioneurotic edema. Absence of serum inhibitor of C′1-esterase. Am. J. Med 35(1):37–44

4. Rosen FS, Charache P, Pensky J et al (1965) Hereditary angioneurotic edema: two genetic variants. Science (80-. ) 148(3672):957–958

5. Cicardi M, Zuraw BL (2018) Angioedema due to bradykinin dysregulation. J Allergy Clin Immunol Pract 6(4):1132–1141

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1. Impact of genetic structural variants in factor XI deficiency: identification, accurate characterization, and inferred mechanism by long-read sequencing;Journal of Thrombosis and Haemostasis;2023-07

2. Picomolar Sensitivity Analysis of Multiple Bradykinin-Related Peptides in the Blood Plasma of Patients With Hereditary Angioedema in Remission: A Pilot Study;Frontiers in Allergy;2022-02-11