Konrad Bork

ORCID: 0000-0002-6084-4577 · 2 papers 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…

2004
The Journal of allergy and clinical immunology ·doi:10.1016/j.jaci.2004.06.047

Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of facial, laryngeal, genital, or peripheral swelling or abdominal pain secondary to intra-abdominal edema. Resulting from mutations affecting C1…