Shigella sonnei meningitis due to interleukin-1 receptor-associated kinase-4 deficiency: first association with a primary immune deficiency. by Chapel, H, Puel, A, von Bernuth, H, Picard, C, Casanova, J

Segmental Uniparental Disonny of Chromosome 12 Causing IRAK-4 Deficiency by Prando, C, Vincent, Q, Puel, A, Picard, C, Chapel, H, Boisson-Dupuis, S, Abel, L, Casanova, J

A fast procedure for the detection of defects in Toll-like receptor signaling. by von Bernuth, H, Ku, C, Rodriguez-Gallego, C, Zhang, S, Garty, B, Maródi, L, Chapel, H, Chrabieh, M, Miller, R, Picard, C, Puel, A, Casanova, J

IRAK4 deficiency presenting with anti-NMDAR encephalitis and HHV6 reactivation by Nishimura, S, Kobayashi, Y, Ohnishi, H, Moriya, K, Tsumura, M, Sakata, S, Mizoguchi, Y, Takada, H, Kato, Z, Sancho-Shimizu, V, Picard, C, Irani, S, Ohara, O, Casanova, J-L, Puel, A, Ishikawa, N, Okada, S, Kobayashi, M

Rpsamutations in isolated congenital asplenia (ICA): A ribosomopathy unveiled by Bosch, B, Bolze, A, Boisson, B, Antipenko, A, Itan, Y, Copley, R, Sackstein, P, Kini, U, Pollard, A, Kumararatne, D, Pac, M, Von Bernuth, H, Selleri, L, Puel, A, Picard, C, Mahlaoui, N, Casanova, J

Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia. by Bolze, A, Mahlaoui, N, Byun, M, Turner, B, Trede, N, Ellis, SR, Abhyankar, A, Itan, Y, Patin, E, Brebner, S, Sackstein, P, Puel, A, Picard, C, Abel, L, Quintana-Murci, L, Faust, SN, Williams, A, Baretto, R, Duddridge, M, Kini, U, Pollard, A, Gaud, C, Frange, P, Orbach, D, Emile, J

Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia by Bolze, A, Mahlaoui, N, Byun, M, Turner, B, Trede, N, Ellis, SR, Abhyankar, A, Itan, Y, Patin, E, Brebner, S, Sackstein, P, Puel, A, Picard, C, Abel, L, Quintana-Murci, L, Faust, SN, Williams, A, Baretto, R, Duddridge, M, Kini, U, Pollard, A, Gaud, C, Frange, P, Orbach, D, Emile, J

Human TLR-7-, -8-, and -9-mediated induction of IFN-alpha/beta and -lambda Is IRAK-4 dependent and redundant for protective immunity to viruses. by Yang, K, Puel, A, Zhang, S, Eidenschenk, C, Ku, C, Casrouge, A, Picard, C, von Bernuth, H, Senechal, B, Plancoulaine, S, Al-Hajjar, S, Al-Ghonaium, A, Maródi, L, Davidson, D, Speert, D, Roifman, C, Garty, B, Ozinsky, A, Barrat, F, Coffman, R, Miller, R, Li, X, Lebon, P, Rodriguez-Gallego, C, Chapel, H

Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells. by de Beaucoudrey, L, Puel, A, Filipe-Santos, O, Cobat, A, Ghandil, P, Chrabieh, M, Feinberg, J, von Bernuth, H, Samarina, A, Jannière, L, Fieschi, C, Stéphan, J, Boileau, C, Lyonnet, S, Jondeau, G, Cormier-Daire, V, Le Merrer, M, Hoarau, C, Lebranchu, Y, Lortholary, O, Chandesris, M, Tron, F, Gambineri, E, Bianchi, L, Rodriguez-Gallego, C

Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons by Bolze, A, Boisson, B, Bosch, B, Antipenko, A, Bouaziz, M, Sackstein, P, Chaker-Margot, M, Barlogis, V, Briggs, T, Colino, E, Elmore, A, Fischer, A, Genel, F, Hewlett, A, Jedidi, M, Kelecic, J, Krüger, R, Ku, C, Kumararatne, D, Lefevre-Utile, A, Loughlin, S, Mahlaoui, N, Markus, S, Garcia, J, Nizon, M, Oleastro, M, Pac, M, Picard, C, Pollard, A, Rodriguez-Gallego, C, Thomas, C, Von Bernuth, H, Worth, A, Meyts, I, Risolino, M, Selleri, L, Puel, A, Klinge, S, Abel, L, Casanova, J