Results 81 to 90 of about 144,374 (198)

Algorithms in Allergy: Hereditary Angioedema

open access: yes
Allergy, Volume 81, Issue 8, Page 3008-3012, August 2026.
Konrad Bork   +3 more
wiley   +1 more source

C1 esterase inhibitor (C1–INH) response as a supportive diagnostic criterion for patients with suspected hereditary angioedema with normal C1–INH

open access: yesWorld Allergy Organization Journal
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

open access: yesJournal of Interdisciplinary Medicine, 2016
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

open access: yes
Clinical &Experimental Allergy, Volume 56, Issue 8, Page 986-988, August 2026.
Roman Hakl   +10 more
wiley   +1 more source

Pathophysiology of hereditary angioedema

open access: yes, 2014
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]

open access: yes, 2010
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

open access: yesClinical and Translational Allergy
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

open access: yesFrontiers in Pediatrics
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

Unveiling Rare Genetic Variants in DAB2IP: New Insights Into the Pathogenesis of Recurrent Angioedema

open access: yes
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

open access: yes, 2015
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  

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