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pro vyhledávání: '"Gedeon Loules, MSc"'
Autor:
Denis Vincent, MD, PhD, Faidra Parsopoulou, PharmD, PhD, Ludovic Martin, MD, PhD, Christine Gaboriaud, PhD, Jacques Demongeot, MD, PhD, Gedeon Loules, MSc, Sascha Fischer, MSc, Sven Cichon, PhD, Anastasios E. Germenis, MD, PhD, Arije Ghannam, MD, PhD, Christian Drouet, PharmD, PhD
Publikováno v:
Journal of Allergy and Clinical Immunology: Global, Vol 3, Iss 2, Pp 100223- (2024)
Background: Hereditary angioedema (HAE) is a potentially life-threatening disorder characterized by recurrent episodes of subcutaneous or submucosal swelling. HAE with normal C1 inhibitor (HAE-nC1-INH) is an underdiagnosed condition. Although the ass
Externí odkaz:
https://doaj.org/article/41f1c6812c6d4fdbad48b9ea2e9deeea