This symposium provided an overview of past, current, and future therapies and routes of administration for patients with hereditary angioedema (HAE). Prof Cicardi opened the symposium by welcoming attendees and introducing the main topics of the session. Prof Magerl then focussed on treatments that are currently used for acute and prophylactic management of patients with HAE and highlighted that there is an unmet medical need in terms of better prophylactic treatment options. Prof Craig summarised the clinical evidence gathered over the last decades and shared the key findings and insights that led to our current understanding of the disease and laid the foundations for current and future treatment approaches. Prof Zuraw presented the find...
Several treatment modalities have become available for management of acute hereditary angioedema (HA...
Introduction: Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a debilitating ...
Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...
Abstract Hereditary angioedema (HAE) is a rare, mostly inherited disorder however 25% of patients...
Hereditary angioedema (HAE) is a chronic disease with a high burden of disease that is poorly unders...
Hereditary angioedema (HAE) is a rare disease that causes episodic attacks of subcutaneous and submu...
Angioedema owing to hereditary deficiency of C1 inhibitor (HAE) is a rare, life-threatening, disabli...
Hereditary angioedema due to C1 inhibitor (C1 esterase inhibitor) deficiency (types I and II HAE-C1-...
Abstract: Current strategies for the treatment of hereditary angio-edema (HAE) include targeted inhi...
Hereditary angioedema (HAE) is a rare genetic condition that manifests as painful and potentially li...
Abstract: Hereditary angioedema (HAE) caused by C1-esterase inhib-itor deficiency is an autosomal-do...
Introduction: Hereditary angioedema (HAE) usually results from C1 inhibitor (C1-INH) deficiency or d...
Hereditary angioedema (HAE) is due to inherited deficiency of C1-inhibitor (C1-INH) and causes local...
Introduction: Hereditary angioedema due to C1-INH deficiency (C1-INH-HAE) is a rare disease with unp...
Hereditary angioedema (HAE) is an autosomal dominantly inherited orphan disease manifested by recurr...
Several treatment modalities have become available for management of acute hereditary angioedema (HA...
Introduction: Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a debilitating ...
Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...
Abstract Hereditary angioedema (HAE) is a rare, mostly inherited disorder however 25% of patients...
Hereditary angioedema (HAE) is a chronic disease with a high burden of disease that is poorly unders...
Hereditary angioedema (HAE) is a rare disease that causes episodic attacks of subcutaneous and submu...
Angioedema owing to hereditary deficiency of C1 inhibitor (HAE) is a rare, life-threatening, disabli...
Hereditary angioedema due to C1 inhibitor (C1 esterase inhibitor) deficiency (types I and II HAE-C1-...
Abstract: Current strategies for the treatment of hereditary angio-edema (HAE) include targeted inhi...
Hereditary angioedema (HAE) is a rare genetic condition that manifests as painful and potentially li...
Abstract: Hereditary angioedema (HAE) caused by C1-esterase inhib-itor deficiency is an autosomal-do...
Introduction: Hereditary angioedema (HAE) usually results from C1 inhibitor (C1-INH) deficiency or d...
Hereditary angioedema (HAE) is due to inherited deficiency of C1-inhibitor (C1-INH) and causes local...
Introduction: Hereditary angioedema due to C1-INH deficiency (C1-INH-HAE) is a rare disease with unp...
Hereditary angioedema (HAE) is an autosomal dominantly inherited orphan disease manifested by recurr...
Several treatment modalities have become available for management of acute hereditary angioedema (HA...
Introduction: Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a debilitating ...
Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant dise...