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Results:
1-16
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Results: 16
Authors:
Doffinger, R
Smahi, A
Bessia, C
Geissmann, F
Feinberg, J
Durandy, A
Bodemer, C
Kenwrick, S
Dupuis-Girod, S
Blanche, S
Wood, P
Rabia, SH
Headon, DJ
Overbeek, PA
Le Deist, F
Holland, SM
Belani, K
Kumararatne, DS
Fischer, A
Shapiro, R
Conley, ME
Reimund, E
Kalhoff, H
Abinun, M
Munnich, A
Israel, A
Courtois, G
Casanova, JL
Citation: R. Doffinger et al., X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappa B signaling, NAT GENET, 27(3), 2001, pp. 277-285
Authors:
Durandy, A
Honjo, T
Citation: A. Durandy et T. Honjo, Human genetic defects in class-switch recombination (hyper-IgM syndromes), CURR OP IM, 13(5), 2001, pp. 543-548
Authors:
Durandy, A
Citation: A. Durandy, Development of specific immunity during prenatal life., ARCH PED, 8(9), 2001, pp. 979-985
Authors:
Ferrari, S
Giliani, S
Insalaco, A
Al-Ghonaium, A
Soresina, AR
Loubser, M
Avanzini, MA
Marconi, M
Badolato, R
Ugazio, AG
Levy, Y
Catalan, N
Durandy, A
Tbakhi, A
Notarangelo, LD
Plebani, A
Citation: S. Ferrari et al., Mutations of CD40 gene cause an autosomal recessive form of immunodeficiency with hyper IgM, P NAS US, 98(22), 2001, pp. 12614-12619
Authors:
Meffre, E
Catalan, N
Seltz, F
Fischer, A
Nussenzweig, MC
Durandy, A
Citation: E. Meffre et al., Somatic hypermutation shapes the antibody repertoire of memory B cells in humans, J EXP MED, 194(3), 2001, pp. 375-378
Authors:
Haddad, E
Paczesny, S
Leblond, V
Seigneurin, JM
Stern, M
Achkar, A
Bauwens, M
Delwail, V
Debray, D
Duvoux, C
Hubert, P
de Ligny, BH
Wijdenes, J
Durandy, A
Fischer, A
Citation: E. Haddad et al., Treatment of B-lymphoproliferative disorder with a monoclonal anti-interleukin-6 antibody in 12 patients: a multicenter phase 1-2 clinical trial, BLOOD, 97(6), 2001, pp. 1590-1597
Authors:
Minegishi, Y
Lavoie, A
Cunningham-Rundles, C
Bedard, PM
Hebert, J
Cote, L
Dan, K
Sedlak, D
Buckley, RH
Fischer, A
Durandy, A
Conley, ME
Citation: Y. Minegishi et al., Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome, CLIN IMMUNO, 97(3), 2000, pp. 203-210
Authors:
Bachmeyer, C
Monge, M
Cazier, A
Le Deist, F
de Saint Basile, G
Durandy, A
Fischer, A
Mougeot-Martin, M
Citation: C. Bachmeyer et al., Gastric adenocarcinoma in a patient with X-linked agammaglobulinaemia, EUR J GASTR, 12(9), 2000, pp. 1033-1035
Authors:
Revy, P
Levy, Y
Geissmann, F
Fischer, A
Durandy, A
Citation: P. Revy et al., Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper-IgM syndrome, M S-MED SCI, 16(10), 2000, pp. 1142-1144
Authors:
Durandy, A
Citation: A. Durandy, Development of the specific immune system in the foetus and neonate., REV FR ALLE, 40(1), 2000, pp. 65-69
Authors:
Revy, P
Muto, T
Levy, Y
Geissmann, F
Plebani, A
Sanal, O
Catalan, N
Forveille, M
Dufourcq-Lagelouse, R
Gennery, A
Tezcan, I
Ersoy, F
Kayserili, H
Ugazio, AG
Brousse, N
Muramatsu, M
Notarangelo, LD
Kinoshita, K
Honjo, T
Fischer, A
Durandy, A
Citation: P. Revy et al., Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper-IgM syndrome (HIGM2), CELL, 102(5), 2000, pp. 565-575
Authors:
Revy, P
Busslinger, M
Tashiro, K
Arenzana, F
Pillet, P
Fischer, A
Durandy, A
Citation: P. Revy et al., A syndrome involving intrauterine growth retardation, microcephaly, cerebellar hypoplasia, B lymphocyte deficiency, and progressive pancytopenia, PEDIATRICS, 105(3), 2000, pp. E391-E395
Authors:
Revy, P
Hivroz, C
Andreu, G
Graber, P
Martinache, C
Fischer, A
Durandy, A
Citation: P. Revy et al., Activation of the janus kinase 3-STAT5a pathway after CD40 triggering of human monocytes but not of resting B cells, J IMMUNOL, 163(2), 1999, pp. 787-793
Authors:
Geissmann, F
Revy, P
Regnault, A
Lepelletier, Y
Dy, M
Brousse, N
Amigorena, S
Hermine, O
Durandy, A
Citation: F. Geissmann et al., TGF-beta 1 prevents the noncognate maturation of human dendritic Langerhans cells, J IMMUNOL, 162(8), 1999, pp. 4567-4575
Authors:
de Saint Basile, G
Tabone, MD
Durandy, A
Phan, F
Fischer, A
Le Deist, F
Citation: G. De Saint Basile et al., CD40 ligand expression deficiency in a female carrier of the X-linked hyper-IgM syndrome as a result of X chromosome lyonization, EUR J IMMUN, 29(1), 1999, pp. 367-373
Authors:
Altare, F
Lammas, D
Revy, P
Jouanguy, E
Doffinger, R
Lamhamedi, S
Drysdale, P
Scheel-Toellner, D
Girdlestone, J
Darbyshire, P
Wadhwa, M
Dockrell, H
Salmon, M
Fischer, A
Durandy, A
Casanova, JL
Kumararatne, DS
Citation: F. Altare et al., Inherited interleukin 12 deficiency in a child with bacille Calmette-Guerin and Salmonella enteritidis disseminated infection, J CLIN INV, 102(12), 1998, pp. 2035-2040
Risultati:
1-16
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