Fremeaux-Bacchi V - Search Results

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. 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.

2

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.

3

Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome.

Fremeaux-Bacchi V, Dragon-Durey MA, Blouin J, Vigneau C, Kuypers D, Boudailliez B, Loirat C, Rondeau E, Fridman WH. Fremeaux-Bacchi V, et al. J Med Genet. 2004 Jun;41(6):e84. doi: 10.1136/jmg.2004.019083. J Med Genet. 2004. PMID: 15173250 Free PMC article. No abstract available.

4

Late-onset thrombocytic microangiopathy caused by cblC disease: association with a factor H mutation.

Guigonis V, Frémeaux-Bacchi V, Giraudier S, Favier R, Borderie D, Massy Z, Mougenot B, Rosenblatt DS, Deschênes G. Guigonis V, et al. Am J Kidney Dis. 2005 Mar;45(3):588-95. doi: 10.1053/j.ajkd.2004.12.004. Am J Kidney Dis. 2005. PMID: 15754282

5

A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation.

Nilsson SC, Karpman D, Vaziri-Sani F, Kristoffersson AC, Salomon R, Provot F, Fremeaux-Bacchi V, Trouw LA, Blom AM. Nilsson SC, et al. Mol Immunol. 2007 Mar;44(8):1835-44. doi: 10.1016/j.molimm.2006.10.005. Epub 2006 Nov 7. Mol Immunol. 2007. PMID: 17084897 Clinical Trial.

6

Unusual clinical severity of complement membrane cofactor protein-associated hemolytic-uremic syndrome and uniparental isodisomy.

Fremeaux-Bacchi V, Sanlaville D, Menouer S, Blouin J, Dragon-Durey MA, Fischbach M, Vekemans M, Fridman WH. Fremeaux-Bacchi V, et al. Am J Kidney Dis. 2007 Feb;49(2):323-9. doi: 10.1053/j.ajkd.2006.10.022. Am J Kidney Dis. 2007. PMID: 17261436

7

Recurrence of hemolytic uremic syndrome after renal transplantation.

Seitz B, Albano L, Vocila F, Mzoughi S, Aoudia R, Guitard J, Ribes D, Vachet-Copponat H, Mourad G, Bienaimé F, Dahan P, Frémeaux-Bacchi V, Cassuto E. Seitz B, et al. Transplant Proc. 2007 Oct;39(8):2583-5. doi: 10.1016/j.transproceed.2007.08.021. Transplant Proc. 2007. PMID: 17954182

8

Does hemolytic uremic syndrome differ from thrombotic thrombocytopenic purpura?

Fakhouri F, Frémeaux-Bacchi V. Fakhouri F, et al. Nat Clin Pract Nephrol. 2007 Dec;3(12):679-87. doi: 10.1038/ncpneph0670. Nat Clin Pract Nephrol. 2007. PMID: 18033227 Review.

9

Complement factor H deficiency and posttransplantation glomerulonephritis with isolated C3 deposits.

Boyer O, Noël LH, Balzamo E, Guest G, Biebuyck N, Charbit M, Salomon R, Frémeaux-Bacchi V, Niaudet P. Boyer O, et al. Am J Kidney Dis. 2008 Apr;51(4):671-7. doi: 10.1053/j.ajkd.2007.11.032. Am J Kidney Dis. 2008. PMID: 18371543

10

Complement mutation-associated de novo thrombotic microangiopathy following kidney transplantation.

Le Quintrec M, Lionet A, Kamar N, Karras A, Barbier S, Buchler M, Fakhouri F, Provost F, Fridman WH, Thervet E, Legendre C, Zuber J, Frémeaux-Bacchi V. Le Quintrec M, et al. Am J Transplant. 2008 Aug;8(8):1694-701. doi: 10.1111/j.1600-6143.2008.02297.x. Epub 2008 Jun 28. Am J Transplant. 2008. PMID: 18557729 Free article.

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