Hereditary angioedema with C1 inhibitor deficiency: delay in diagnosis in Europe
Hereditary angioedema with C1 inhibitor deficiency: delay in diagnosis in Europe
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Author / Creator
Publisher
England: BioMed Central Ltd
Journal title
Language
English
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Publication information
Publisher
England: BioMed Central Ltd
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Scope and Contents
Contents
Hereditary angioedema (HAE) is a rare, debilitating, and potentially life-threatening disease characterized by recurrent edema attacks. Important advances in HAE treatment have been made, including the development of new therapies for treating or preventing attacks. Nevertheless, the disease is still frequently misdiagnosed and inappropriately trea...
Alternative Titles
Full title
Hereditary angioedema with C1 inhibitor deficiency: delay in diagnosis in Europe
Authors, Artists and Contributors
Author / Creator
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Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3751114
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3751114
Other Identifiers
ISSN
1710-1484,1710-1492
E-ISSN
1710-1492
DOI
10.1186/1710-1492-9-29
