Common variable immunodeficiency disorders: division into distinct clinical phenotypes. حسب Chapel, H, Lucas, M, Lee, M, Bjorkander, J, Webster, D, Grimbacher, B, Fieschi, C, Thon, V, Abedi, MR, Hammarstrom, L

Efficiency of immunoglobulin G replacement therapy in common variable immunodeficiency: correlations with clinical phenotype and polymorphism of the neonatal Fc receptor. حسب Gouilleux-Gruart, V, Chapel, H, Chevret, S, Lucas, M, Malphettes, M, Fieschi, C, Patel, S, Boutboul, D, Marson, M, Gérard, L, Lee, M, Watier, H, Oksenhendler, E

Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells. حسب 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

Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency حسب Cottineau, J, Kottemann, M, Lach, F, Kang, Y, Vély, F, Deenick, E, Lazarov, T, Gineau, L, Wang, Y, Farina, A, Chansel, M, Lorenzo, L, Piperoglou, C, Ma, C, Nitschke, P, Belkadi, A, Itan, Y, Boisson, B, Jabot-Hanin, F, Picard, C, Bustamante, J, Eidenschenk, C, Boucherit, S, Aladjidi, N, Lacombe, D, Barat, P, Qasim, W, Hurst, J, Pollard, A, Uhlig, H, Fieschi, C, Michon, J, Bermudez, V, Abel, L, de Villartay, J, Geissmann, F, Tangye, S, Hurwitz, J, Vivier, E, Casanova, J, Smogorzewska, A, Jouanguy, E