Abdominal attacks and treatment in hereditary angioedema with C1-inhibitor deficiency
Open Access
- 9 April 2014
- journal article
- clinical trial
- Published by Springer Nature in BMC Gastroenterology
- Vol. 14 (1), 71
- https://doi.org/10.1186/1471-230X-14-71
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- US Hereditary Angioedema Association Medical Advisory Board 2013 Recommendations for the Management of Hereditary Angioedema Due to C1 Inhibitor DeficiencyThe Journal of Allergy and Clinical Immunology: In Practice, 2013
- Leukocytosis and high hematocrit levels during abdominal attacks of hereditary angioedemaBMC Gastroenterology, 2013
- Ecallantide for treatment of acute hereditary angioedema attacks: Analysis of efficacy by patient characteristicsAllergy and Asthma Proceedings, 2012
- Physician approaches to beta-lactam use in patients with penicillin hypersensitivityAllergy and Asthma Proceedings, 2012
- Many faces of angioedemaEuropean Journal of Gastroenterology & Hepatology, 2012
- 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedemaAllergy, Asthma & Clinical Immunology, 2010
- Hereditary AngioedemaNew England Journal of Medicine, 2008
- Successful resolution of bowel obstruction in a patient with hereditary angioedemaEuropean Journal of Gastroenterology & Hepatology, 2008
- Treatment with C1 inhibitor concentrate in abdominal pain attacks of patients with hereditary angioedemaTransfusion, 2005
- Hereditary angioneurotic oedema: an unusual case of recurring abdominal painGut, 1970