Frémeaux-Bacchi V - Search Results

1

Rare Variants in Complement Gene in C3 Glomerulopathy and Immunoglobulin-Mediated Membranoproliferative GN.

Meuleman MS, Vieira-Martins P, El Sissy C, Audard V, Baudouin V, Bertrand D, Bridoux F, Louillet F, Dossier C, Esnault V, Jourde-Chiche N, Karras A, Morin MP, Provot F, Remy P, Ribes D, Rousset-Rouviere C, Servais A, Thervet E, Tricot L, Zaidan M, Wynckel A, Zuber J, Le Quintrec M, Frémeaux-Bacchi V, Chauvet S. Meuleman MS, et al. Clin J Am Soc Nephrol. 2023 Nov 1;18(11):1435-1445. doi: 10.2215/CJN.0000000000000252. Epub 2023 Aug 24. Clin J Am Soc Nephrol. 2023. PMID: 37615951 Free PMC article.

2

[Acquired C1 inhibitor deficiency associated with lymphoproliferative disorders: four cases].

Bibi-Triki T, Eclache V, Frilay Y, Stirnemann J, Frémeaux-Bacchi V, Fain O. Bibi-Triki T, et al. Rev Med Interne. 2004 Sep;25(9):667-72. doi: 10.1016/j.revmed.2004.06.003. Rev Med Interne. 2004. PMID: 15363623 French.

3

Functional analysis of splicing mutations and of an exon 2 polymorphic variant of SERPING1/C1NH.

Duponchel C, Djenouhat K, Frémeaux-Bacchi V, Monnier N, Drouet C, Tosi M. Duponchel C, et al. Hum Mutat. 2006 Mar;27(3):295-6. doi: 10.1002/humu.9414. Hum Mutat. 2006. PMID: 16470590

4

Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome.

Vaziri-Sani F, Holmberg L, Sjöholm AG, Kristoffersson AC, Manea M, Frémeaux-Bacchi V, Fehrman-Ekholm I, Raafat R, Karpman D. Vaziri-Sani F, et al. Kidney Int. 2006 Mar;69(6):981-8. doi: 10.1038/sj.ki.5000155. Kidney Int. 2006. PMID: 16528247 Free article.

5

Molecular basis of a selective C1s deficiency associated with early onset multiple autoimmune diseases.

Dragon-Durey MA, Quartier P, Frémeaux-Bacchi V, Blouin J, de Barace C, Prieur AM, Weiss L, Fridman WH. Dragon-Durey MA, et al. J Immunol. 2001 Jun 15;166(12):7612-6. doi: 10.4049/jimmunol.166.12.7612. J Immunol. 2001. PMID: 11390518

6

[Pathophysiology of thrombotic microangiopathies: current understanding].

Coppo P, Veyradier A, Durey MA, Fremeaux-Bacchi V, Scrobohaci ML, Amesland F, Bussel A. Coppo P, et al. Ann Med Interne (Paris). 2002 May;153(3):153-66. Ann Med Interne (Paris). 2002. PMID: 12218898 Review. French.

7

Membrane and soluble forms of CD21 (the C3dg/EBV receptor).

Frémeaux-Bacchi V, Fischer E, Kazatchkine MD. Frémeaux-Bacchi V, et al. Immunol Lett. 1996 Dec;54(2-3):201-4. doi: 10.1016/s0165-2478(96)02673-9. Immunol Lett. 1996. PMID: 9052878 Review. No abstract available.

8

A new type of acquired C1 inhibitor deficiency associated with systemic lupus erythematosus.

Cacoub P, Frémeaux-Bacchi V, De Lacroix I, Guillien F, Kahn MF, Kazatchkine MD, Godeau P, Piette JC. Cacoub P, et al. Arthritis Rheum. 2001 Aug;44(8):1836-40. doi: 10.1002/1529-0131(200108)44:8<1836::AID-ART321>3.0.CO;2-Y. Arthritis Rheum. 2001. PMID: 11508436 Free article.

9

No lupus nephritis in the absence of antiC1q autoantibodies?

Frémeaux-Bacchi V, Noël LH, Schifferli JA. Frémeaux-Bacchi V, et al. Nephrol Dial Transplant. 2002 Dec;17(12):2041-3. doi: 10.1093/ndt/17.12.2041. Nephrol Dial Transplant. 2002. PMID: 12454207 Review. No abstract available.

10

Human complement factor H deficiency associated with hemolytic uremic syndrome.

Rougier N, Kazatchkine MD, Rougier JP, Fremeaux-Bacchi V, Blouin J, Deschenes G, Soto B, Baudouin V, Pautard B, Proesmans W, Weiss E, Weiss L. Rougier N, et al. J Am Soc Nephrol. 1998 Dec;9(12):2318-26. doi: 10.1681/ASN.V9122318. J Am Soc Nephrol. 1998. PMID: 9848786

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