Dynamics of complement activation in aHUS and how to monitor eculizumab therapy

Atypical hemolytic-uremic syndrome (aHUS) is associated with genetic complement abnormalities/anti–complement factor H antibodies, which paved the way to treatment with eculizumab. We studied 44 aHUS patients and their relatives to (1) test new assays of complement activation, (2) verify whether suc...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Noris, Marina, Galbusera, Miriam, Gastoldi, Sara, Macor, Paolo, Banterla, Federica, Bresin, Elena, Tripodo, Claudio, Bettoni, Serena, Donadelli, Roberta, Valoti, Elisabetta, Tedesco, Francesco, Amore, Alessandro, Coppo, Rosanna, Ruggenenti, Piero, Gotti, Eliana, Remuzzi, Giuseppe
Format: Artigo
Idioma:Inglês
Publicat: American Society of Hematology 2014
Matèries:
Clinical Trials and Observations
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4162105/
https://ncbi.nlm.nih.gov/pubmed/25037630
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2014-02-558296
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars