Add to ORKGAttacks of laryngeal edema in patients with hereditary angioedema (HAE) have been successfully treated with the infusion of C1-inhibitor (C1-INH) concentrate. No side effects were observed
Abstract Background Acquired angioedema due to C1-inhibitor (C1-INH) deficiency (AAE-C1-INH) is a se...
One hundred and four patients affected by hereditary angioedema belonging to 31 families have been s...
Hereditary angioedema (HAE) is a rarely seen disorder of C1 inhibitor (C1-INH) deficiency usually ma...
C1-inhibitor (C1-INH) deficiency is the genetic defect underlying hereditary angioedema (HAE). Subje...
Background: Plasma-derived C1 inhibitor (C1-INH) concentrate is a treatment option for acute heredit...
Hereditary angioedema is a rare autosomal dominant disease characterized by recurrent episodes of an...
Hereditary angioedema (HAE), a rare autosomal dominant genetic disorder, is caused by a deficiency i...
Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a rare genetic disease charac...
C1-inhibitor deficiency can be inherited or acquired; both conditions lead to recurrent angioedema t...
Hereditary angioedema (HAE) is due to inherited deficiency of C1-inhibitor (C1-INH) and causes local...
Abstract Hereditary angioedema (HAE) is a rare autosomal dominant disease most commonl...
Hereditary angioedema (HAE) is arare, potentially life-threatening au-tosomal dominant disease cause...
Hereditary angioedema is an autosomal‑dominant disorder caused by mutation of the gene encoding the ...
Purpose of review Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency (C1-INH-HAE) i...
Hereditary angioedema (HAE) is due to the inherited deficiency of C1-Inhibitor (C1-Inh). When specif...
Abstract Background Acquired angioedema due to C1-inhibitor (C1-INH) deficiency (AAE-C1-INH) is a se...
One hundred and four patients affected by hereditary angioedema belonging to 31 families have been s...
Hereditary angioedema (HAE) is a rarely seen disorder of C1 inhibitor (C1-INH) deficiency usually ma...
C1-inhibitor (C1-INH) deficiency is the genetic defect underlying hereditary angioedema (HAE). Subje...
Background: Plasma-derived C1 inhibitor (C1-INH) concentrate is a treatment option for acute heredit...
Hereditary angioedema is a rare autosomal dominant disease characterized by recurrent episodes of an...
Hereditary angioedema (HAE), a rare autosomal dominant genetic disorder, is caused by a deficiency i...
Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a rare genetic disease charac...
C1-inhibitor deficiency can be inherited or acquired; both conditions lead to recurrent angioedema t...
Hereditary angioedema (HAE) is due to inherited deficiency of C1-inhibitor (C1-INH) and causes local...
Abstract Hereditary angioedema (HAE) is a rare autosomal dominant disease most commonl...
Hereditary angioedema (HAE) is arare, potentially life-threatening au-tosomal dominant disease cause...
Hereditary angioedema is an autosomal‑dominant disorder caused by mutation of the gene encoding the ...
Purpose of review Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency (C1-INH-HAE) i...
Hereditary angioedema (HAE) is due to the inherited deficiency of C1-Inhibitor (C1-Inh). When specif...
Abstract Background Acquired angioedema due to C1-inhibitor (C1-INH) deficiency (AAE-C1-INH) is a se...
One hundred and four patients affected by hereditary angioedema belonging to 31 families have been s...
Hereditary angioedema (HAE) is a rarely seen disorder of C1 inhibitor (C1-INH) deficiency usually ma...