PW01-032 – FMF-like state: genetic factors unrelated to MEFV

por Babikyan, D, Jeru, I, Copin, B, Hayrapetyan, H, Amselem, S, Sarkisian, T
Publicado 2013

P02-014 - Consequences of Arginine 92 mutations in TNFR1

por Jéru, I, Charmion, S, Cochet, E, Copin, B, Le Borgne, G, Cathebras, P, Gaillat, J, Duquesnoy, P, Karabina, S, Hentgen, V, Amselem, S
Publicado 2013

A heterozygous variant in MEFV in a familial autoinflammatory syndrome with PAPA-like features

por Jéru, I, Van Eyck, L, Lagou, V, Ruuth-Praz, J, Copin, B, Cochet, E, Liston, A, Goris, A, Amselem, S, Wouters, C
Publicado 2015

OR13-003 - TNFRSF11A molecular defects cause autoinflammatory disorders

por Jéru, I, Cochet, E, Duquesnoy, P, Hentgen, V, Copin, B, Mitjavila-Garcia, M, Sheykholeslami, S, Le Borgne, G, Dastot, F, Karabina, S, Mahevas, M, Chantot-Bastaraud, S, Faivre, L, Amselem, S
Publicado 2013

Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia

por Legendre, M, Blanchon, S, Copin, B, Duquesnoy, P, Montantin, G, Kott, E, Dastot, F, Jeanson, L, Cachanado, M, Rousseau, A, Papon, JF, Tamalet, A, Vojtek, AM, Escalier, D, Coste, A, de Blic, J, Clément, A, Escudier, E, Amselem, S
Publicado 2012