The hereditary angioedema burden of illness study in Europe (HAE-BOIS-Europe): background and methodology
Open Access
- 26 April 2012
- journal article
- Published by Springer Science and Business Media LLC in BMC Dermatology
- Vol. 12 (1), 4
- https://doi.org/10.1186/1471-5945-12-4
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedemaAllergy, Asthma & Clinical Immunology, 2010
- Economic costs associated with acute attacks and long-term management of hereditary angioedemaAnnals of Allergy, Asthma & Immunology, 2010
- Hereditary angio-oedema in Denmark: a nationwide surveyBritish Journal of Dermatology, 2009
- Impact Of The Frankfurt HAE Therapy Protocol On Health-Related Quality Of Life (HRQoL) In 50 Patients With Hereditary Angioedema (HAE)Journal of Allergy and Clinical Immunology, 2009
- Hereditary AngioedemaThe New England Journal of Medicine, 2008
- Development of an Specific Questionnaire for the Assessment of Health-Related Quality of Life in Adult Patients with Hereditary Angioedema due to C1 inhibitor Deficiency (HAE) and Cross-Cultural Validation proposalJournal of Allergy and Clinical Immunology, 2008
- The establishment and utility of Sweha-Reg: a Swedish population-based registry to understand hereditary angioedemaBMC Dermatology, 2007
- Hereditary Angioedema: New Findings Concerning Symptoms, Affected Organs, and CourseThe American Journal of Medicine, 2006
- How Many Interviews Are Enough?Field Methods, 2006
- Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyondJournal of Allergy and Clinical Immunology, 2004