A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy
A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy
About this item
Full title
Author / Creator
Zanichelli, Andrea , Arcoleo, Francesco , Barca, Maria , Borrelli, Paolo , Bova, Maria , Cancian, Mauro , Cicardi, Marco , Cillari, Enrico , De Carolis, Caterina , De Pasquale, Tiziana , Del Corso, Isabella , Di Rocco, Paola , Guarino, Maria , Massaro, Ilaria , Minale, Paola , Montinaro, Vincenzo , Neri, Sergio , Perricone, Roberto , Pucci, Stefano , Quattrocchi, Paolina , Rossi, Oliviero , Triggiani, Massimo , Zanierato, Giuseppina and Zoli, Alessandra
Publisher
England: BioMed Central Ltd
Journal title
Language
English
Formats
Publication information
Publisher
England: BioMed Central Ltd
Subjects
More information
Scope and Contents
Contents
Hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE type I) or dysfunction (C1-INH-HAE type II) is a rare disease characterized by recurrent episodes of edema with an estimated frequency of 1:50,000 in the global population without racial or gender differences. In this study we present the results of a nationwide survey of C1-INH-HAE p...
Alternative Titles
Full title
A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy
Authors, Artists and Contributors
Author / Creator
Arcoleo, Francesco
Barca, Maria
Borrelli, Paolo
Bova, Maria
Cancian, Mauro
Cicardi, Marco
Cillari, Enrico
De Carolis, Caterina
De Pasquale, Tiziana
Del Corso, Isabella
Di Rocco, Paola
Guarino, Maria
Massaro, Ilaria
Minale, Paola
Montinaro, Vincenzo
Neri, Sergio
Perricone, Roberto
Pucci, Stefano
Quattrocchi, Paolina
Rossi, Oliviero
Triggiani, Massimo
Zanierato, Giuseppina
Zoli, Alessandra
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4333895
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4333895
Other Identifiers
ISSN
1750-1172
E-ISSN
1750-1172
DOI
10.1186/s13023-015-0233-x
