Background: Recombinant human C1 esterase inhibitor (rhC1-INH) is approved for treatment of hereditary angioedema (HAE) in adolescents and adults. HAE attacks that involve the upper airway can be life threatening, and data on the administration of rhC1-INH for these types of attacks are currently limited. Objective: To evaluate the efficacy and safety of rhC1-INH for treatment of acute HAE attacks with upper airway involvement. Methods: A pooled analysis of data from three clinical trials with open-label extensions examined rhC1-INH for treatment of acute HAE attacks with upper airway involvement. Patients with functional plasma C1 esterase inhibitor <50% of normal who had experienced an acute upper airway HAE attack and received ...
Introduction: Hereditary angioedema due to C1-inhibitor (C1-INH-HAE) is a rare disease characterized...
Background Agents for prophylaxis of hereditary angioedema (HAE) have been available in the United S...
Abstract Hereditary angioedema (HAE) is a rare autosomal dominant disease most commonl...
Background Hereditary angioedema (HAE), caused by C1 inhibitor (C1INH) deficiency or dysfunction, is...
BackgroundHereditary angioedema (HAE) caused by a deficiency in functional C1 esterase inhibitor (C1...
Hereditary angioedema (HAE) is a rare genetic condition characterised by recurring attacks of local ...
Hereditary angioedema (HAE), a rare autosomal dominant genetic disorder, is caused by a deficiency i...
Background: Hereditary angioedema caused by C1 esterase inhibitor deficiency is a rare disorder. O...
Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...
Introduction: Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a debilitating ...
Abstract: Hereditary angioedema (HAE) caused by C1-esterase inhib-itor deficiency is an autosomal-do...
Background: For the prevention of attacks of hereditary angioedema (HAE), the efficacy and safety of...
Introduction: Angioedema is a localized and self-limiting edema of the subcutaneous and submucosal t...
AbstractBackgroundHereditary angioedema (HAE) is a rare disease characterized by C1-esterase inhibit...
Background: Plasma-derived C1 inhibitor (C1-INH) concentrate is a treatment option for acute heredit...
Introduction: Hereditary angioedema due to C1-inhibitor (C1-INH-HAE) is a rare disease characterized...
Background Agents for prophylaxis of hereditary angioedema (HAE) have been available in the United S...
Abstract Hereditary angioedema (HAE) is a rare autosomal dominant disease most commonl...
Background Hereditary angioedema (HAE), caused by C1 inhibitor (C1INH) deficiency or dysfunction, is...
BackgroundHereditary angioedema (HAE) caused by a deficiency in functional C1 esterase inhibitor (C1...
Hereditary angioedema (HAE) is a rare genetic condition characterised by recurring attacks of local ...
Hereditary angioedema (HAE), a rare autosomal dominant genetic disorder, is caused by a deficiency i...
Background: Hereditary angioedema caused by C1 esterase inhibitor deficiency is a rare disorder. O...
Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...
Introduction: Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a debilitating ...
Abstract: Hereditary angioedema (HAE) caused by C1-esterase inhib-itor deficiency is an autosomal-do...
Background: For the prevention of attacks of hereditary angioedema (HAE), the efficacy and safety of...
Introduction: Angioedema is a localized and self-limiting edema of the subcutaneous and submucosal t...
AbstractBackgroundHereditary angioedema (HAE) is a rare disease characterized by C1-esterase inhibit...
Background: Plasma-derived C1 inhibitor (C1-INH) concentrate is a treatment option for acute heredit...
Introduction: Hereditary angioedema due to C1-inhibitor (C1-INH-HAE) is a rare disease characterized...
Background Agents for prophylaxis of hereditary angioedema (HAE) have been available in the United S...
Abstract Hereditary angioedema (HAE) is a rare autosomal dominant disease most commonl...