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Page 1
Campylobacter infection in adult patients with primary antibody deficiency.
J Allergy Clin Immunol Pract. 2019 Mar;7(3):1038-1041.e4. doi: 10.1016/j.jaip.2018.06.014. Epub 2018 Jul 6.
J Allergy Clin Immunol Pract. 2019.
PMID: 29981862
No abstract available.
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.
Clin Infect Dis. 2008 May 15;46(10):1547-54. doi: 10.1086/587669.
Clin Infect Dis. 2008.
PMID: 18419489
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Exclusion of Patients with a Severe T-Cell Defect Improves the Definition of Common Variable Immunodeficiency.
Bertinchamp R, Gérard L, Boutboul D, Malphettes M, Fieschi C, Oksenhendler E; DEFI study group.
Bertinchamp R, et al.
J Allergy Clin Immunol Pract. 2016 Nov-Dec;4(6):1147-1157. doi: 10.1016/j.jaip.2016.07.002. Epub 2016 Aug 10.
J Allergy Clin Immunol Pract. 2016.
PMID: 27522107
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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
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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.
Clin Infect Dis. 2009 Nov 1;49(9):1329-38. doi: 10.1086/606059.
Clin Infect Dis. 2009.
PMID: 19807277
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Autoimmunity in common variable immunodeficiency: correlation with lymphocyte phenotype in the French DEFI study.
Boileau J, Mouillot G, Gérard L, Carmagnat M, Rabian C, Oksenhendler E, Pasquali JL, Korganow AS; DEFI Study Group.
Boileau J, et al.
J Autoimmun. 2011 Feb;36(1):25-32. doi: 10.1016/j.jaut.2010.10.002. Epub 2010 Nov 13.
J Autoimmun. 2011.
PMID: 21075598
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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.
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