Subcellular localisation of marenostrin/pyrin isoforms carrying the most common mutations involved in familial Mediterranean fever in the presence or absence of its binding partner...

Por Cazeneuve, C, Papin, S, Jeru, I, Duquesnoy, P, Amselem, S
Publicado em 2004

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

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

PW03-034 – How to classify autoinflammatory diseases?

Por Grateau, G, Hentgen, V, Stankovic, K, Jéru, I, Amselem, S, Steichen, O
Publicado em 2013

Rationale and efficacy of interleukin-1 targeting in pediatric Erdheim- Chester disease

Por Kone-Paut I, Delwail A, Jéru I, Lecron JC, Pariente D, Tran TA, Meinzer U
Publicado em 2011-09-01

Rationale and efficacy of interleukin-1 targeting in pediatric Erdheim- Chester disease

Por Tran, TA, Lecron, JC, Pariente, D, Jéru, I, Delwail, A, Kone-Paut, I, Meinzer, U
Publicado em 2011

PW01-022 – Dissociation between CRP and SAA in FMF

Por Stojanovic, K Stankovic, Hentgen, V, Georgin-Lavialle, S, Fellahi, S, Jeru, I, Amselem, S, Bastard, J-P, Grateau, G
Publicado em 2013

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