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Functional C1-inhibitor diagnostics in hereditary angioedema: assay evaluation and recommendations.
Wagenaar-Bos IG, Drouet C, Aygören-Pursun E, Bork K, Bucher C, Bygum A, Farkas H, Fust G, Gregorek H, Hack CE, Hickey A, Joller-Jemelka HI, Kapusta M, Kreuz W, Longhurst H, Lopez-Trascasa M, Madalinski K, Naskalski J, Nieuwenhuys E, Ponard D, Truedsson L, Varga L, Nielsen EW, Wagner E, Zingale L, Cicardi M, van Ham SM. Wagenaar-Bos IG, et al. Among authors: drouet c. J Immunol Methods. 2008 Sep 30;338(1-2):14-20. doi: 10.1016/j.jim.2008.06.004. Epub 2008 Jul 23. J Immunol Methods. 2008. PMID: 18655790
Acquired C1-inhibitor deficiency: 7 patients treated with rituximab.
Branellec A, Bouillet L, Javaud N, Mekinian A, Boccon-Gibod I, Blanchard-Delaunay C, Oksenhendler E, Ollivier Y, Dunogué B, Amarger S, Ponard D, Drouet C, Mouthon L, Thomas M, Fain O; French National Reference Center for Angioedema (CREAK). Branellec A, et al. Among authors: drouet c. J Clin Immunol. 2012 Oct;32(5):936-41. doi: 10.1007/s10875-012-9691-2. Epub 2012 Apr 20. J Clin Immunol. 2012. PMID: 22526593
SERPING1 and F12 combined variants in a hereditary angioedema family.
Charignon D, Ponard D, de Gennes C, Drouet C, Ghannam A. Charignon D, et al. Among authors: drouet c. Ann Allergy Asthma Immunol. 2018 Oct;121(4):500-502. doi: 10.1016/j.anai.2018.05.031. Epub 2018 Jun 6. Ann Allergy Asthma Immunol. 2018. PMID: 29885370 No abstract available.
International Consensus on the Use of Genetics in the Management of Hereditary Angioedema.
Germenis AE, Margaglione M, Pesquero JB, Farkas H, Cichon S, Csuka D, Lera AL, Rijavec M, Jolles S, Szilagyi A, Trascasa ML, Veronez CL, Drouet C, Zamanakou M; Hereditary Angioedema International Working Group. Germenis AE, et al. Among authors: drouet c. J Allergy Clin Immunol Pract. 2020 Mar;8(3):901-911. doi: 10.1016/j.jaip.2019.10.004. Epub 2019 Oct 24. J Allergy Clin Immunol Pract. 2020. PMID: 31669336 Review.
180 results