Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema

Por Deroux, A., Boccon‐Gibod, I., Fain, O., Pralong, P., Ollivier, Y., Pagnier, A., Djenouhat, K., Du‐Thanh, A., Gompel, A., Faisant, C., Launay, D., Bouillet, L.
Publicado no Clin Exp Immunol (2016)

PReS-FINAL-2191: Imaging of chronic recurrent multifocal osteitis: a french national cohort of 178 cases

Por Wipff, J, Nouar, D, Lemelle, I, Pajot, C, Duquesne, A, Lorrot, M, Faye, A, Bader-Meunier, B, Brochard, K, Despert, V, Jean, S, Grall-Lerosey, M, Marot, Y, Pagnier, A, Quartier, P, Deslandre, C
Publicado em 2013