Hereditary Angioedema Types I and II

Known as: Deficiency of C1 Esterase Inhibitor, Hereditary Angioedema Types I and II [Disease/Finding], C1 Esterase Inhibitor, Deficiency Of 
Autosomal dominant inherited disorders characterized by abnormalities of C1 inhibitor. Patients present with swelling of the skin, subcutaneous… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

2006-2016
01220062016

Papers overview

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2014
2014
  • Regis Albuquerque CamposI, Alfeu Tavares FrançaII, +7 authors Anete Sevciovic GrumachIX
  • 2014
CONTEXT AND OBJECTIVE: Hereditary angioedema (HAE) with C1 inhibitor deficiency manifests as recurrent episodes of edema… (More)
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2012
2012
Hereditary angioedema is a genetic disorder due to a deficiency or malfunction of C1 esterase inhibitor. We herein describe a… (More)
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2012
2012
CONTEXT AND OBJECTIVE: An association between chronic idiopathic urticaria (CIU) and autoimmune thyroid disease (ATD) has been… (More)
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Review
2006
Review
2006
Hereditary angioedema is a congenital disorder with recurrent attacks of localized swelling of submucosal and subcutaneous tissue… (More)
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