Results 81 to 90 of about 144,374 (198)
Algorithms in Allergy: Hereditary Angioedema
Allergy, Volume 81, Issue 8, Page 3008-3012, August 2026.
Konrad Bork +3 more
wiley +1 more source
Diagnosis of hereditary angioedema (HAE) with normal C1INH level (HAE-nl-C1INH) is based on several criteria, including either an associated genetic variant identified or family history of recurrent angioedema plus lack of high-dose antihistamine ...
Andrew M. Smith, MD +11 more
doaj +1 more source
Hereditary Angioedema: a Challenging Diagnosis for the Gastroenterologist
Hereditary angioedema (HAE) caused by a deficiency of C1 esterase inhibitor enzyme (C1-INH) is a very rare, autosomal dominantly inherited genetic disorder, characterized by recurrent peripheral angioedema, painful abdominal attacks and episodes of ...
Gábos Gabriella +2 more
doaj +1 more source
Registry‐Based Analysis of Treatment and Retreatment Attacks of Hereditary Angioedema
Clinical &Experimental Allergy, Volume 56, Issue 8, Page 986-988, August 2026.
Roman Hakl +10 more
wiley +1 more source
Pathophysiology of hereditary angioedema
The genetic deficiency of the C1 inhibitor is responsible for hereditary angioedema (HAE), which is a disease transmitted as an autosomal dominant trait.
M. Cicardi +5 more
core +1 more source
Management of hereditary angioedema: 2010 Canadian approach [PDF]
C1-inhibitor (C1-INH) deficiency is a rare blood disorder resulting in angioedema attacks that are debilitating and may be life-threatening. Prophylaxis and therapy of events has changed since our first Canadian Consensus Conference on the diagnosis ...
John Brosz +9 more
core +1 more source
Treatment of Hereditary Angioedema With Plasma‐Derived C1 Inhibitor: A Review
Hereditary angioedema (HAE) is clinically characterized by recurrent episodes of localized edema. HAE typically occurs due to a deficiency of functional C1 inhibitor (C1INH, HAE‐C1INH); in addition, several types of HAE with normal quantity and activity ...
Inmaculada Martinez‐Saguer +3 more
doaj +1 more source
Case Report: Early presentation of hereditary angioedema symptoms in a 2-year-old boy
Hereditary angioedema (HAE) is a rare autosomal-dominant disease that is caused by a deficiency (type I) or dysfunction (type II) of the C1 inhibitor (C1-INH) due to a mutation in the SERPING1 gene, which codes for C1-INH.
Jurate Staikuniene-Kozonis +5 more
doaj +1 more source
Allergy, Volume 81, Issue 7, Page 2519-2522, July 2026.
Maurizio Margaglione +8 more
wiley +1 more source
Management of acute attacks of hereditary angioedema: role of ecallantide
Hannah Duffey,1 Rafael Firszt1,2 1Department of Pediatrics, 2Division of Allergy, Immunology and Rheumatology, University of Utah, Salt Lake City, UT, USA Abstract: Hereditary angioedema (HAE) is characterized as an episodic swelling disorder with ...
Firszt R, Duffey H
core

