Fortschritte in Diagnostik und Therapie des hereditären Angioödems
Author:
Publisher
Springer Science and Business Media LLC
Subject
Earth-Surface Processes
Link
https://link.springer.com/content/pdf/10.1007/s15012-022-6896-9.pdf
Reference19 articles.
1. Busse PJ et al. Hereditary Angioedema. N Engl J Med. 2020; 382: 1136-48
2. Bafunno V et al. Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema. J Allergy Clin Immunol. 2018; 141: 1009-17
3. Ariano A et al. A myoferlin gain-of-function variant associates with a new type of hereditary angioedema. Allergy. 2020; 75: 2989-92
4. Donaldson VH et al. A Biochemical Abnormality in Herediatry Angioneurotic Edema: Absence of Serum Inhibitor of C' 1-Esterase. Am J Med. 1963; 35: 37-44
5. Bork K et al. A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor. Clin Immunol Orlando Fla. 2011; 141: 31-5
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