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Page 1
Complement Activation and Thrombotic Microangiopathy Associated With Monoclonal Gammopathy: A National French Case Series.
Martins M, Bridoux F, Goujon JM, Meuleman MS, Ribes D, Rondeau E, Guerry MJ, Delmas Y, Levy B, Ducloux D, Kandel-Aznar C, Le Fur A, Garrouste C, Provot F, Gibier JB, Thervet E, Bruneval P, Rabant M, Karras A, Dragon Durey MA, Fremeaux-Bacchi V, Chauvet S. Martins M, et al. Among authors: dragon durey ma. Am J Kidney Dis. 2022 Sep;80(3):341-352. doi: 10.1053/j.ajkd.2021.12.014. Epub 2022 Feb 22. Am J Kidney Dis. 2022. PMID: 35217094 Free article.
Restricted genetic defects underlie human complement C6 deficiency.
Dragon-Durey MA, Fremeaux-Bacchi V, Blouin J, Barraud D, Fridman WH, Kazatchkine MD. Dragon-Durey MA, et al. Clin Exp Immunol. 2003 Apr;132(1):87-91. doi: 10.1046/j.1365-2249.2003.02099.x. Clin Exp Immunol. 2003. PMID: 12653841 Free PMC article.
[Investigation of the complement system in clinical practice].
Frémeaux-Bacchi V, Dragon-Durey MA, Blouin J, Mouthon L, Fridman WH. Frémeaux-Bacchi V, et al. Among authors: dragon durey ma. Ann Med Interne (Paris). 2003 Dec;154(8):529-40. Ann Med Interne (Paris). 2003. PMID: 15037829 Review. French.
[Complement component deficiencies in human disease].
Dragon-Durey MA, Fremeaux-Bacchi V. Dragon-Durey MA, et al. Presse Med. 2006 May;35(5 Pt 2):861-70. doi: 10.1016/s0755-4982(06)74705-4. Presse Med. 2006. PMID: 16710159 Review. French.
Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome.
Fremeaux-Bacchi V, Moulton EA, Kavanagh D, Dragon-Durey MA, Blouin J, Caudy A, Arzouk N, Cleper R, Francois M, Guest G, Pourrat J, Seligman R, Fridman WH, Loirat C, Atkinson JP. Fremeaux-Bacchi V, et al. Among authors: dragon durey ma. J Am Soc Nephrol. 2006 Jul;17(7):2017-25. doi: 10.1681/ASN.2005101051. Epub 2006 Jun 8. J Am Soc Nephrol. 2006. PMID: 16762990
111 results