Fremeaux-Bacchi V - Search Results

1

Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome.

Sellier-Leclerc AL, Fremeaux-Bacchi V, Dragon-Durey MA, Macher MA, Niaudet P, Guest G, Boudailliez B, Bouissou F, Deschenes G, Gie S, Tsimaratos M, Fischbach M, Morin D, Nivet H, Alberti C, Loirat C; French Society of Pediatric Nephrology. Sellier-Leclerc AL, et al. J Am Soc Nephrol. 2007 Aug;18(8):2392-400. doi: 10.1681/ASN.2006080811. Epub 2007 Jun 28. J Am Soc Nephrol. 2007. PMID: 17599974

2

Complete inherited deficiency of the fourth complement component in a child with systemic lupus erythematosus and his disease-free brother in a north African family.

Fremeaux-Bacchi V, Uring-Lambert B, Weiss L, Brun P, Blouin J, Hartmann D, Loirat C, Hauptmann G, Kazatchkine MD. Fremeaux-Bacchi V, et al. J Clin Immunol. 1994 Sep;14(5):273-9. doi: 10.1007/BF01540980. J Clin Immunol. 1994. PMID: 7814456

3

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

4

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

5

Successful plasma therapy in hemolytic uremic syndrome with factor H deficiency.

Nathanson S, Frémeaux-Bacchi V, Deschênes G. Nathanson S, et al. Pediatr Nephrol. 2001 Jul;16(7):554-6. doi: 10.1007/s004670100609. Pediatr Nephrol. 2001. PMID: 11465803

6

Prevalence of monoclonal gammopathy in patients presenting with acquired angioedema type 2.

Frémeaux-Bacchi V, Guinnepain MT, Cacoub P, Dragon-Durey MA, Mouthon L, Blouin J, Cherin P, Laurent J, Piette JC, Fridman WH, Weiss L, Kazatchkine MO. Frémeaux-Bacchi V, et al. Am J Med. 2002 Aug 15;113(3):194-9. doi: 10.1016/s0002-9343(02)01124-5. Am J Med. 2002. PMID: 12208377

7

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.

8

Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases.

Dragon-Durey MA, Frémeaux-Bacchi V, Loirat C, Blouin J, Niaudet P, Deschenes G, Coppo P, Herman Fridman W, Weiss L. Dragon-Durey MA, et al. J Am Soc Nephrol. 2004 Mar;15(3):787-95. doi: 10.1097/01.asn.0000115702.28859.a7. J Am Soc Nephrol. 2004. PMID: 14978182

9

[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. Ann Med Interne (Paris). 2003 Dec;154(8):529-40. Ann Med Interne (Paris). 2003. PMID: 15037829 Review. French.

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

353 results

Search Page

Filters