Abstract Background Hereditary angioedema (HAE) due to C1 esterase inhibitor (C1-INH) deficiency is characterized by recurrent swelling attacks that can be life-threatening if left untreated. Prompt treatment is vital during acute attacks; plasma-derived C1-INH (Berinert®) is one treatment currently licensed for the intravenous treatment of acute HAE attacks in adults, adolescents and children. A new, volume-reduced formulation, of C1-INH is currently available which aims to reduce the time to treatment, and provide greater convenience to patients and healthcare professionals. Here we compare the clinical experience of the reduced volume 1500 IU vial with multiple 500 IU vials. Methods HAE patients treated with C1-INH at the Royal London Ho...
Introduction: Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a debilitating ...
Background Hereditary angioedema (HAE), caused by C1 inhibitor (C1INH) deficiency or dysfunction, is...
Hereditary angioedema (HAE), a rare autosomal dominant genetic disorder, is caused by a deficiency i...
Background: Plasma-derived C1 inhibitor (C1-INH) concentrate is a treatment option for acute heredit...
Background: Over 40 years of use demonstrates that complement 1 esterase inhibitor (C1-INH) concentr...
Background: Hereditary angioedema caused by C1 esterase inhibitor deficiency is a rare disorder. O...
Abstract Background Hereditary angioedema with C1 inhibitor deficiency is a disabling, potentially f...
C1-inhibitor (C1-INH) deficiency is the genetic defect underlying hereditary angioedema (HAE). Subje...
Abstract Hereditary angioedema (HAE) is a rare autosomal dominant disease most commonl...
Background Hereditary angioedema (HAE) is a rare disease caused by C1-esterase inhibitor (C1-INH) de...
BackgroundThe plasma-derived, highly purified, nanofiltered C1-inhibitor concentrate (Berinert; “pnf...
Background The plasma-derived, pasteurized, nanofiltered C1-inhibitor concentrate (pnfC1-INH) is app...
Abstract Introduction For prophylaxis of hereditary angioedema (HAE) attacks, replacement therapy wi...
Background Agents for prophylaxis of hereditary angioedema (HAE) have been available in the United S...
Attacks of hereditary angioedema with C1 inhibitor deficiency (C1-INH-HAE) are commonly treated in t...
Introduction: Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a debilitating ...
Background Hereditary angioedema (HAE), caused by C1 inhibitor (C1INH) deficiency or dysfunction, is...
Hereditary angioedema (HAE), a rare autosomal dominant genetic disorder, is caused by a deficiency i...
Background: Plasma-derived C1 inhibitor (C1-INH) concentrate is a treatment option for acute heredit...
Background: Over 40 years of use demonstrates that complement 1 esterase inhibitor (C1-INH) concentr...
Background: Hereditary angioedema caused by C1 esterase inhibitor deficiency is a rare disorder. O...
Abstract Background Hereditary angioedema with C1 inhibitor deficiency is a disabling, potentially f...
C1-inhibitor (C1-INH) deficiency is the genetic defect underlying hereditary angioedema (HAE). Subje...
Abstract Hereditary angioedema (HAE) is a rare autosomal dominant disease most commonl...
Background Hereditary angioedema (HAE) is a rare disease caused by C1-esterase inhibitor (C1-INH) de...
BackgroundThe plasma-derived, highly purified, nanofiltered C1-inhibitor concentrate (Berinert; “pnf...
Background The plasma-derived, pasteurized, nanofiltered C1-inhibitor concentrate (pnfC1-INH) is app...
Abstract Introduction For prophylaxis of hereditary angioedema (HAE) attacks, replacement therapy wi...
Background Agents for prophylaxis of hereditary angioedema (HAE) have been available in the United S...
Attacks of hereditary angioedema with C1 inhibitor deficiency (C1-INH-HAE) are commonly treated in t...
Introduction: Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a debilitating ...
Background Hereditary angioedema (HAE), caused by C1 inhibitor (C1INH) deficiency or dysfunction, is...
Hereditary angioedema (HAE), a rare autosomal dominant genetic disorder, is caused by a deficiency i...