Results 11 to 20 of about 594 (209)
Over diagnosis of bradykinin angioedema in patients treated with angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers [PDF]
World Allergy Organization Journal, 2023 Background: Bradykinin angioedemas are a potentially serious side effect of angiotensin-converting enzyme inhibitors (ACEI) and more controversially of angiotensin II receptor blockers (ARB).
O Dereure, Aurélie Du-Thanh
exaly +4 more sources
The characteristics of upper airway edema in hereditary and acquired angioedema with C1‐inhibitor deficiency [PDF]
Clinical and Translational Allergy, 2021 Background Angioedemas localized in the upper airway are potentially life threatening, and without proper treatment, they may lead to death by suffocation. Upper airway edemas (UAE) in bradykinin‐mediated angioedemas can even be the first symptoms of the
Zsuzsanna Balla +2 more
exaly +3 more sources
Angioedemas associated with renin-angiotensin system blocking drugs: Comparative analysis of spontaneous adverse drug reaction reports [PDF]
PLoS ONE, 2020 IntroductionAngioedema is a subcutaneous swelling typically affecting the face, larynx or pharynx. It is a known adverse drug reaction (ADR) of ACE inhibitors (ACEi), angiotensin-II-receptor blockers (ARBs) and aliskiren (renin inhibitor).
Diana Dubrall +2 more
exaly +3 more sources
Hereditary angioedema prevalence and satisfaction with prophylaxis in South Australia [PDF]
World Allergy Organization JournalBackground: Hereditary angioedema (HAE) due to deficiency of C1 Inhibitor (C1INH-HAE) is a rare, unpredictable and potentially fatal genetic disorder. There are relatively few systematic population prevalence studies, with reports from various countries ...
Alexander Troelnikov, Pravin Hissaria
exaly +4 more sources
Complex analysis of the national Hereditary angioedema cohort in Slovakia – Identification of 12 novel variants in SERPING1 gene [PDF]
World Allergy Organization JournalBackground: Hereditary angioedema (HAE) is a rare autosomal dominant genetic disease characterised by acute episodes of non-pruritic skin and submucosal swelling caused by increase in vascular permeability.
Adam Markocsy, MD +11 more
doaj +2 more sources
A case of angioedema of hereditary origin in a rural clinic near Subotica [PDF]
ABC: časopis urgentne medicine, 2023 Introduction: Hereditary angioedema (HAE) is inherited in an autosomal dominant manner. It manifests with bradykinin-mediated swelling due to a deficiency of C1 inhibitor.
Gavrilović Nikola +2 more
doaj +1 more source
Long-term prophylaxis of hereditary angioedema [PDF]
Liječnički vjesnik, 2022 Hereditary angioedema (HAE) is a rare inherited disease characterized by recurrent attacks of painful swelling of the subcutaneous and submucosal tissues.
Dijana Perković +8 more
doaj +1 more source
Deutsches Ärzteblatt international, 2017 Acute angioedema of the upper airways can be life-threatening. An important distinction is drawn between mast-cell-mediated angioedema and bradykinin-mediated angioedema; the treatment of these two entities is fundamentally different.This review is based on pertinent articles retrieved by a selective search in PubMed and on guidelines concerning the ...
Janina, Hahn +5 more
openaire +4 more sources
Urticaria and Angioedema [PDF]
Immunology and Allergy Clinics of North America, 2011 Urticaria (hives) is a common disorder that often presents with angioedema (swelling that occurs beneath the skin). It is generally classified as acute, chronic or physical. Second-generation, non-sedating H1-receptor antihistamines represent the mainstay of therapy for both acute and chronic urticaria. Angioedema can occur in the absence of urticaria,
Kanani Amin +2 more
+8 more sources
World Allergy Organization Journal, 2023 Background: Given the recent approval of oral berotralstat in several countries for hereditary angioedema (HAE) prophylaxis, transition from long-term androgens to berotralstat may occur in clinical practice.
Jonny G. Peter, MB ChB, MMed, FCP (SA), PhD +4 more
doaj +1 more source