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Page 1
Infections in 252 patients with common variable immunodeficiency.
Oksenhendler E, Gérard L, Fieschi C, Malphettes M, Mouillot G, Jaussaud R, Viallard JF, Gardembas M, Galicier L, Schleinitz N, Suarez F, Soulas-Sprauel P, Hachulla E, Jaccard A, Gardeur A, Théodorou I, Rabian C, Debré P; DEFI Study Group. Oksenhendler E, et al. Among authors: mouillot g. Clin Infect Dis. 2008 May 15;46(10):1547-54. doi: 10.1086/587669. Clin Infect Dis. 2008. PMID: 18419489
Late-onset combined immune deficiency: a subset of common variable immunodeficiency with severe T cell defect.
Malphettes M, Gérard L, Carmagnat M, Mouillot G, Vince N, Boutboul D, Bérezné A, Nove-Josserand R, Lemoing V, Tetu L, Viallard JF, Bonnotte B, Pavic M, Haroche J, Larroche C, Brouet JC, Fermand JP, Rabian C, Fieschi C, Oksenhendler E; DEFI Study Group. Malphettes M, et al. Among authors: mouillot g. Clin Infect Dis. 2009 Nov 1;49(9):1329-38. doi: 10.1086/606059. Clin Infect Dis. 2009. PMID: 19807277
Parental consanguinity is associated with a severe phenotype in common variable immunodeficiency.
Rivoisy C, Gérard L, Boutboul D, Malphettes M, Fieschi C, Durieu I, Tron F, Masseau A, Bordigoni P, Alric L, Haroche J, Hoarau C, Bérézné A, Carmagnat M, Mouillot G, Oksenhendler E; DEFI study group. Rivoisy C, et al. Among authors: mouillot g. J Clin Immunol. 2012 Feb;32(1):98-105. doi: 10.1007/s10875-011-9604-9. Epub 2011 Oct 15. J Clin Immunol. 2012. PMID: 22002594
B-cell and T-cell phenotypes in CVID patients correlate with the clinical phenotype of the disease.
Mouillot G, Carmagnat M, Gérard L, Garnier JL, Fieschi C, Vince N, Karlin L, Viallard JF, Jaussaud R, Boileau J, Donadieu J, Gardembas M, Schleinitz N, Suarez F, Hachulla E, Delavigne K, Morisset M, Jacquot S, Just N, Galicier L, Charron D, Debré P, Oksenhendler E, Rabian C; DEFI Study Group. Mouillot G, et al. J Clin Immunol. 2010 Sep;30(5):746-55. doi: 10.1007/s10875-010-9424-3. Epub 2010 May 1. J Clin Immunol. 2010. PMID: 20437084
Protective effect of IgM against colonization of the respiratory tract by nontypeable Haemophilus influenzae in patients with hypogammaglobulinemia.
Micol R, Kayal S, Mahlaoui N, Beauté J, Brosselin P, Dudoit Y, Obenga G, Barlogis V, Aladjidi N, Kebaili K, Thomas C, Dulieu F, Monpoux F, Nové-Josserand R, Pellier I, Lambotte O, Salmon A, Masseau A, Galanaud P, Oksenhendler E, Tabone MD, Teira P, Coignard-Biehler H, Lanternier F, Join-Lambert O, Mouillot G, Theodorou I, Lecron JC, Alyanakian MA, Picard C, Blanche S, Hermine O, Suarez F, Debré M, Lecuit M, Lortholary O, Durandy A, Fischer A. Micol R, et al. Among authors: mouillot g. J Allergy Clin Immunol. 2012 Mar;129(3):770-7. doi: 10.1016/j.jaci.2011.09.047. Epub 2011 Dec 6. J Allergy Clin Immunol. 2012. PMID: 22153772
Defects in the CD19 complex predispose to glomerulonephritis, as well as IgG1 subclass deficiency.
Vince N, Boutboul D, Mouillot G, Just N, Peralta M, Casanova JL, Conley ME, Bories JC, Oksenhendler E, Malphettes M, Fieschi C; DEFI Study Group. Vince N, et al. Among authors: mouillot g. J Allergy Clin Immunol. 2011 Feb;127(2):538-541.e1-5. doi: 10.1016/j.jaci.2010.10.019. Epub 2010 Dec 14. J Allergy Clin Immunol. 2011. PMID: 21159371 No abstract available.
Efficiency of immunoglobulin G replacement therapy in common variable immunodeficiency: correlations with clinical phenotype and polymorphism of the neonatal Fc receptor.
Gouilleux-Gruart V, Chapel H, Chevret S, Lucas M, Malphettes M, Fieschi C, Patel S, Boutboul D, Marson MN, Gérard L, Lee M, Watier H, Oksenhendler E; DEFI study group. Gouilleux-Gruart V, et al. Clin Exp Immunol. 2013 Feb;171(2):186-94. doi: 10.1111/cei.12002. Clin Exp Immunol. 2013. PMID: 23286945 Free PMC article.
Hypoxia modulates HLA-G gene expression in tumor cells.
Mouillot G, Marcou C, Zidi I, Guillard C, Sangrouber D, Carosella ED, Moreau P. Mouillot G, et al. Hum Immunol. 2007 Apr;68(4):277-85. doi: 10.1016/j.humimm.2006.10.016. Epub 2006 Nov 27. Hum Immunol. 2007. PMID: 17400064
14 results