LE PATOIS DE GONDECOURT.

Por COCHET,E.
Publicado em C193

OR2-002 – The risk of FMF in MEFV heterozygotes

Por Jéru, I, Hentgen, V, Cochet, E, Duquesnoy, P, Le Borgne, G, Grimprel, E, Stojanovic, K Stankovic, Karabina, S, Grateau, G, Amselem, S
Publicado em 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 em 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 no Pediatr Rheumatol Online J (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 em 2013

Mutations in NALP12 cause hereditary periodic fever syndromes

Por Jéru, I., Duquesnoy, P., Fernandes-Alnemri, T., Cochet, E., Yu, J. W., Lackmy-Port-Lis, M., Grimprel, E., Landman-Parker, J., Hentgen, V., Marlin, S., McElreavey, K., Sarkisian, T., Grateau, G., Alnemri, E. S., Amselem, S.
Publicado em 2008