A robust multiplexed assay to quantify C1-inhibitor, C1q, and C4 proteins for in vitro diagnosis of hereditary angioedema from dried blood spot
Author:
Funder
Takeda Pharmaceuticals U.S.A.
Publisher
Elsevier BV
Subject
Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry
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2. Pediatric hereditary angioedema due to C1-inhibitor deficiency;Farkas;Allergy Asthma Clin. Immunol.,2010
3. Hereditary angioedema: a broad review for clinicians;Nzeako;Arch. Intern. Med.,2001
4. Functional C1-inhibitor diagnostics in hereditary angioedema: assay evaluation and recommendations;Wagenaar-Bos;J. Immunol. Methods,2008
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1. Acquired Angioedema Due to C1-Inhibitor Deficiency (AAE-C1-INH)—A Bicenter Retrospective Study on Diagnosis, Course, and Therapy;The Journal of Allergy and Clinical Immunology: In Practice;2023-12
2. Application of a dried blood spot based proteomic and genetic assay for diagnosing hereditary angioedema;Clinical and Translational Allergy;2023-11
3. The impact of puberty on the onset, frequency, location, and severity of attacks in hereditary angioedema due to C1-inhibitor deficiency: A survey from the Italian Network for Hereditary and Acquired Angioedema (ITACA);Frontiers in Pediatrics;2023-04-18
4. Current Understanding of Dried Spots Platform for Blood Proteomics;Current Proteomics;2023-04
5. The international WAO/EAACI guideline for the management of hereditary angioedema – The 2021 revision and update;World Allergy Organization Journal;2022-03
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