Hereditary angioedema with normal C1-INH withversuswithout specificF12gene mutations-Reference-Cited by-同舟云学术

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Hereditary angioedema with normal C1-INH withversuswithout specificF12gene mutations

Published:2015-05-22 Issue:8 Volume:70 Page:1004-1012
ISSN:0105-4538
Container-title:Allergy
language:en
Short-container-title:Allergy

Author:

Bork K.¹,Wulff K.²,Witzke G.¹,Hardt J.³

Affiliation:

1. Department of Dermatology; Johannes Gutenberg University; Mainz Germany

2. University Medicine; Ernst Moritz Arndt University; Greifswald Germany

3. Department of Medical Psychology and Medical Sociology; Johannes Gutenberg University; Mainz Germany

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

Reference29 articles.

1. Angioedema;Bork;Immunol Allergy Clin North Am,2014

2. Current update on cellular and molecular mechanisms of hereditary angioedema;Walford;Ann Allergy Asthma Immunol,2014

3. Pathogenic mechanisms of bradykinin mediated diseases: dysregulation of an innate inflammatory pathway;Kaplan;Adv Immunol,2014

4. Hereditary angioedema with normal C1-inhibitor activity in women;Bork;Lancet,2000

5. A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor;Bork;Clin Immunol,2011

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2. Contact System Activation and Bradykinin Generation in Angioedema;Immunology and Allergy Clinics of North America;2024-08

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5. Altered levels of phospholipases C, diacylglycerols, endocannabinoids, and N‐acylethanolamines in patients with hereditary angioedema due to FXII mutation;Allergy;2024-06-27

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