Jochen Hardt

No ORCID on file · 1 paper in corpus
article 2008
·doi:10.1016/s1081-1206(10)60424-3

BackgroundHereditary angioedema (HAE) due to C1 inhibitor deficiency is clinically characterized by relapsing skin swellings, abdominal pain attacks, and life-threatening upper airway obstruction. Treatment with androgens prevents attacks f…