Frémeaux-Bacchi V - Search Results

1

An international consensus approach to the management of atypical hemolytic uremic syndrome in children.

Loirat C, Fakhouri F, Ariceta G, Besbas N, Bitzan M, Bjerre A, Coppo R, Emma F, Johnson S, Karpman D, Landau D, Langman CB, Lapeyraque AL, Licht C, Nester C, Pecoraro C, Riedl M, van de Kar NC, Van de Walle J, Vivarelli M, Frémeaux-Bacchi V; HUS International. Loirat C, et al. Pediatr Nephrol. 2016 Jan;31(1):15-39. doi: 10.1007/s00467-015-3076-8. Epub 2015 Apr 11. Pediatr Nephrol. 2016. PMID: 25859752 Review.

2

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

3

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

4

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

5

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.

6

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome.

Dragon-Durey MA, Loirat C, Cloarec S, Macher MA, Blouin J, Nivet H, Weiss L, Fridman WH, Frémeaux-Bacchi V. Dragon-Durey MA, et al. J Am Soc Nephrol. 2005 Feb;16(2):555-63. doi: 10.1681/ASN.2004050380. Epub 2004 Dec 8. J Am Soc Nephrol. 2005. PMID: 15590760

7

The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts.

Fremeaux-Bacchi V, Kemp EJ, Goodship JA, Dragon-Durey MA, Strain L, Loirat C, Deng HW, Goodship TH. Fremeaux-Bacchi V, et al. J Med Genet. 2005 Nov;42(11):852-6. doi: 10.1136/jmg.2005.030783. Epub 2005 Mar 22. J Med Genet. 2005. PMID: 15784724 Free PMC article.

8

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.

9

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. 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

10

Secondary failure of plasma therapy in factor H deficiency.

Nathanson S, Ulinski T, Frémeaux-Bacchi V, Deschênes G. Nathanson S, et al. Pediatr Nephrol. 2006 Nov;21(11):1769-71. doi: 10.1007/s00467-006-0237-9. Epub 2006 Aug 15. Pediatr Nephrol. 2006. PMID: 16909242

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