A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy

INTRODUCTION: 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 stu...

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Detalles Bibliográficos
Publicado en:Orphanet J Rare Dis
Main Authors: Zanichelli, Andrea, Arcoleo, Francesco, Barca, Maria Pina, Borrelli, Paolo, Bova, Maria, Cancian, Mauro, Cicardi, Marco, Cillari, Enrico, De Carolis, Caterina, De Pasquale, Tiziana, Del Corso, Isabella, Di Rocco, Paola Cesinaro, Guarino, Maria Domenica, Massaro, Ilaria, Minale, Paola, Montinaro, Vincenzo, Neri, Sergio, Perricone, Roberto, Pucci, Stefano, Quattrocchi, Paolina, Rossi, Oliviero, Triggiani, Massimo, Zanierato, Giuseppina, Zoli, Alessandra
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2015
Assuntos:
Research
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4333895/
https://ncbi.nlm.nih.gov/pubmed/25758562
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-015-0233-x
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