Angioedema is a rare condition which manifests as sudden localised, non-pitting swelling of
certain body parts including skin and mucous membranes. It is vital that anaesthesiologists …

Background Hereditary angioedema (HAE) is a genetic disorder clinically characterized by
recurrent attacks of subcutaneous and mucosal swelling. 17-α-Alkylated androgens (AA) …

The type II transmembrane serine protease family consists of 18 closely related serine
proteases that are implicated in multiple functions. To identify selective, inhibitory antibodies …

A number of new and innovative approaches for repairing damaged myocardium are
currently undergoing investigation, with several encouraging results. In addition to the …

Diabetic retinal disease is characterized by a series of retinal microvascular changes and
increases in retinal vascular permeability that lead to development of diabetic retinopathy …

Hereditary angioedema (HAE) is a lifelong illness characterized by recurrent swelling of the
skin, intestinal tract, and, ominously, the upper airway. It is caused by inadequate activity of …

RESUMO O angioedema hereditário é uma doença autossômica dominante caracterizada
por crises de edema com o envolvimento de múltiplos órgaos. A doença é desconhecida …

Hereditary angioedema (HAE) with C1 esterase inhibitor (C1-INH) deficiency (C1-INH-HAE)
is a rare disease characterized by diminished levels or dysfunctional activity of C1-INH …

Hereditary angioedema (HAE) due to C1 esterase inhibitor (C1-INH) deficiency (HAE-C1-
INH) is a rare but medically significant disease that can be associated with considerable …

Introduction Hereditary angioedema (HAE) is a rare genetic disorder characterized by
recurrent edema and predominantly caused by the dysregulation of the kinin-kallikrein …