Current treatment options for hereditary angioedema due to C1 inhibitor deficiency
Author:
Publisher
Informa Healthcare
Subject
Pharmacology (medical),Pharmacology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1517/14656566.2016.1104300
Reference96 articles.
1. Papers of special note have been highlighted as either of importance (*) or of considerable importance (**) to readers.
2. Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group
3. A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy
4. Hereditary angio-oedema
5. Mutational Spectrum of the C1 Inhibitor Gene in a Cohort of Italian Patients with Hereditary Angioedema: Description of Nine Novel Mutations
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1. Summary and future of medicine for hereditary angioedema;Drug Discovery Today;2024-03
2. Analysis of coagulation factors in angioedema/urticaria: increased values of D-dimer and fibrinogen in isolated angioedema;Acta Dermatovenerologica Alpina Pannonica et Adriatica;2024
3. Emerging drugs for the treatment of hereditary angioedema due to C1-inhibitor deficiency;Expert Opinion on Emerging Drugs;2022-04-03
4. BRADYKININ MEDIATED GASTROINTESTINAL EDEMA AS A CAUSE OF ABDOMINAL ATTACKS IN PATIENTS WITH HEREDITARY ANGIOEDEMA DUE TO C1-INHIBITOR DEFICIENCY;J PHYSIOL PHARMACOL;2022
5. Population pharmacokinetics of recombinant human C1 esterase inhibitor in children with hereditary angioedema;Annals of Allergy, Asthma & Immunology;2021-06
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