Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study-Reference-Cited by-同舟云学术

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Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study

Published:2016-04-21 Issue:1 Volume:11 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Steiner Urs C.,Weber-Chrysochoou Christina,Helbling Arthur,Scherer Kathrin,Grendelmeier Peter Schmid,Wuillemin Walter A.

Funder

no funding

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics (clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-016-0423-1

Reference32 articles.

1. Agostoni A, Cicardi M. Hereditary and acquired C1-inhibitor deficiency: biological and clinical characteristics in 235 patients. Med (Baltimore). 1992;71(4):206–15.

2. Bork K, Hardt J, Schicketanz KH, Ressel N. Clinical studies of sudden upper airway obstruction in patients with hereditary angio-oedema due to C1 esterase inhibitor deficiency. Arch Inern Med. 2003;163:1229–35.

3. Cicardi M, Aberer W, Banerji A, Bas M, Bernstein JA, Bork K, Caballero T, Farkas H, Grumach A, Kaplan AP, Riedl MA, Triggiani M, Zanichelli A, Zuraw B, on behalf of HAWK, under the patronage of EAACI (European Academy of Allergy and Clinical Immunology). Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group. Allergy. 2014;69:602–16.

4. Zuraw BL. Clinical practice. Hereditary angioedema. N Engl J Med. 2008;359(10):1027–36. doi: 10.1056/NEJMcp0803977 .

5. Bork K. Hereditary angioedema with normal C1 inhibitor. Immunol Allergy Clin North Am. 2013;33(4):457–70. doi: 10.1016/j.iac.2013.07.002 .

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