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The dermatology view of hereditary angioedema: Practical diagnostic and management considerations

Filename 73. Maurer Parish, The dermat. view of HAE, JEADV 2013.pdf
Filesize 403,45 KB
Version r.073
Date added Juni 26, 2020
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Category Reviews
Authors Maurer, M and Parish, L. C.
Citation Maurer, M. and Parish, L. C.: The dermatology view of hereditary angioedema: Practical diagnostic and management considerations. J. Eur. Acad. Dermatol. Venereol. 2013: 27; 133-141.
Corresponding authors Maurer, M
DocNum r.73
DocType PDF
Edition; Page 27; 133-141
IF 2.78
Publisher J. Eur. Acad. Dermatol. Venereol.
ReleaseDate 2013

Hereditary angio-oedema (HAE) is characterized by recurrent, localized, non-pitting, non-pruritic, non-urticarial oedema. Nearly all patients experience skin swelling as a feature of HAE. There may be painful abdominal attacks, accompanied by nausea and vomiting. The disease is life-threatening should laryngeal oedema occur. HAE results from a deficiency or dysfunction of C1 inhibitor, a plasma protein with an important role in regulating the contact, complement and fibrinolytic systems. Effective management of HAE should include a plan for treatment of attacks, as well as routine and preprocedure prevention. Acute and prophylactic therapy with C1 inhibitor therapy for correcting the underlying deficiency in HAE is a valuable option.

Received: 19 December 2011; Accepted: 4 April 2012

 

(Last update: 07.2025)

Number of original publications in peer-reviewed journals:650
Number of reviews in peer-reviewed journals:229
Number of publications (original work and reviews) in peer-reviewed journals:879
Cumulative IF for original publications in peer-reviewed journals:4648.29
Cumulative IF for reviews in peer-reviewed journals:1689.22
Cumulative IF of publications (original work & reviews) in peer-reviewed journals:6761.91
Total number of citations: 45.522, h-index: 109 (Web of Science Juli 2025)45522

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