Associated Papers
Abstracts of the 14th C1-inhibitor Deficiency and Angioedema Workshop.
Unknown Author
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology, 2026
Phenotypic and molecular characterization of the largest worldwide cluster of hereditary angioedema type 1.
Arias-Flórez JS et al.
Plos One, 2024
Clinical and genetic features of hereditary angioedema with and without C1-inhibitor (C1-INH) deficiency in Japan.
Hashimura C et al.
Allergy, 2021
In Search of an Association Between Genotype and Phenotype in Hereditary Angioedema due to C1-INH Deficiency.
Loli-Ausejo D et al.
Clinical Reviews in Allergy & Immunology, 2021
First Analysis of SERPING1 Gene in Patients with Hereditary Angioedema in Colombia Reveals Two Genotypic Variants in a Highly Symptomatic Individual.
Rodríguez JA et al.
Journal of Clinical Immunology, 2018
Hereditary angioedema in Japan: genetic analysis of 13 unrelated cases.
Yamamoto T et al.
The American Journal of the Medical Sciences, 2012
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