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

Mostrar otras versiones (1)

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333895/
https://www.ncbi.nlm.nih.gov/pubmed/25758562
http://dx.doi.org/10.1186/s13023-015-0233-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333895/
https://www.ncbi.nlm.nih.gov/pubmed/25758562
http://dx.doi.org/10.1186/s13023-015-0233-x

Ejemplares similares