Leveraging Genetics for Hereditary Angioedema: A Road Map to Precision Medicine
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Immunology and Allergy
Link
https://link.springer.com/content/pdf/10.1007/s12016-021-08836-7.pdf
Reference119 articles.
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2. Margaglione M, D’Apolito M, Santocroce R, Bruna Maffione A (2019) Hereditary angioedema: looking for BK production and triggers of vascular permeability. Clin Exp Allergy 49:1395–1402
3. Bork K, Barnstedt S, Koch P, Traupe H (2000) Hereditary angioedema with normal C1-inhibitor activity in women. Lancet 356:213–217
4. Binkley K, Davis AE III (2000) Clinical, biochemical, and genetic characterization of a novel estrogen-dependent inherited form of angioedema. J Allergy Clin Immunol 106:546–550
5. Dewald G, Bork K (2006) Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor. Biochem Biophys Res Commun 343:1286–1289
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1. The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency;Gene;2024-08
2. Definition, acronyms, nomenclature, and classification of angioedema (DANCE): AAAAI, ACAAI, ACARE, and APAAACI DANCE consensus;Journal of Allergy and Clinical Immunology;2024-08
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4. Genetic Variants Leading to Urticaria and Angioedema and Associated Biomarkers;The Journal of Allergy and Clinical Immunology: In Practice;2023-08
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