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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Orphanet J Rare Dis
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2015
Gaiak:
Research
Sarrera elektronikoa: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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