Unnecessary Abdominal Surgeries in Attacks of Hereditary Angioedema with Normal C1 Inhibitor
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Immunology and Allergy
Link
https://link.springer.com/content/pdf/10.1007/s12016-021-08852-7.pdf
Reference25 articles.
1. Busse PJ, Christiansen SC, Riedl MA et al (2021) US HAEA medical advisory board 2020 guidelines for the management of hereditary Angioedema. J Allergy Clin Immunol Pract 9(1):132–150.e3. https://doi.org/10.1016/j.jaip.2020.08.0462020.08.046
2. Bork K, Machnig T, Wulff K, Witzke G, Prusty S, Hardt J (2020) Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence. Orphanet J Rare Dis 15(1):289. https://doi.org/10.1186/s13023-020-01570-x
3. Busse PJ, Christiansen SC (2020) Hereditary angioedema. N Engl J Med 382(12):1136–1148. https://doi.org/10.1056/NEJMra1808012
4. Veronez CL, Grumach AS (2020) Angioedema without urticaria: novel findings which must be measured in clinical setting. Curr Opin Allergy Clin Immunol 20(3):253–260. https://doi.org/10.1097/ACI.0000000000000633
5. Cicardi M, Zuraw BL (2018) Angioedema due to bradykinin dysregulation. J Allergy Clin Immunol Pract 6(4):1132–1141. https://doi.org/10.1016/j.jaip.2018.04.0222018.04.022
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2. Managing Diagnosis, Treatment, and Burden of Disease in Hereditary Angioedema Patients with Normal C1-Esterase Inhibitor;Journal of Asthma and Allergy;2023-04
3. BRADYKININ MEDIATED GASTROINTESTINAL EDEMA AS A CAUSE OF ABDOMINAL ATTACKS IN PATIENTS WITH HEREDITARY ANGIOEDEMA DUE TO C1-INHIBITOR DEFICIENCY;J PHYSIOL PHARMACOL;2022
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