Frémeaux-Bacchi V - Search Results

1

Heterogeneous histologic and clinical evolution in 3 cases of dense deposit disease with long-term follow-up.

Figuères ML, Frémeaux-Bacchi V, Rabant M, Galmiche L, Marinozzi MC, Grünfeld JP, Noël LH, Servais A. Figuères ML, et al. Hum Pathol. 2014 Nov;45(11):2326-33. doi: 10.1016/j.humpath.2014.07.021. Epub 2014 Aug 16. Hum Pathol. 2014. PMID: 25260719

2

Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome.

Servais A, Frémeaux-Bacchi V, Lequintrec M, Salomon R, Blouin J, Knebelmann B, Grünfeld JP, Lesavre P, Noël LH, Fakhouri F. Servais A, et al. J Med Genet. 2007 Mar;44(3):193-9. doi: 10.1136/jmg.2006.045328. Epub 2006 Oct 3. J Med Genet. 2007. PMID: 17018561 Free PMC article.

3

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

4

Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome.

Fakhouri F, Jablonski M, Lepercq J, Blouin J, Benachi A, Hourmant M, Pirson Y, Dürrbach A, Grünfeld JP, Knebelmann B, Frémeaux-Bacchi V. Fakhouri F, et al. Blood. 2008 Dec 1;112(12):4542-5. doi: 10.1182/blood-2008-03-144691. Epub 2008 Jul 24. Blood. 2008. PMID: 18658028 Free article.

5

Lupus nephritis associated with complete C1s deficiency efficiently treated with rituximab: a case report.

Bienaimé F, Quartier P, Dragon-Durey MA, Frémeaux-Bacchi V, Bader-Meunier B, Patey N, Salomon R, Noël LH. Bienaimé F, et al. Arthritis Care Res (Hoboken). 2010 Sep;62(9):1346-50. doi: 10.1002/acr.20163. Arthritis Care Res (Hoboken). 2010. PMID: 20191570 Free article. No abstract available.

6

C3 glomerulopathy: a new classification.

Fakhouri F, Frémeaux-Bacchi V, Noël LH, Cook HT, Pickering MC. Fakhouri F, et al. Nat Rev Nephrol. 2010 Aug;6(8):494-9. doi: 10.1038/nrneph.2010.85. Epub 2010 Jul 6. Nat Rev Nephrol. 2010. PMID: 20606628 Review.

7

Heterogeneous pattern of renal disease associated with homozygous factor H deficiency.

Servais A, Noël LH, Dragon-Durey MA, Gübler MC, Rémy P, Buob D, Cordonnier C, Makdassi R, Jaber W, Boulanger E, Lesavre P, Frémeaux-Bacchi V. Servais A, et al. Hum Pathol. 2011 Sep;42(9):1305-11. doi: 10.1016/j.humpath.2010.11.023. Epub 2011 Mar 10. Hum Pathol. 2011. PMID: 21396679

8

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies.

Servais A, Noël LH, Roumenina LT, Le Quintrec M, Ngo S, Dragon-Durey MA, Macher MA, Zuber J, Karras A, Provot F, Moulin B, Grünfeld JP, Niaudet P, Lesavre P, Frémeaux-Bacchi V. Servais A, et al. Kidney Int. 2012 Aug;82(4):454-64. doi: 10.1038/ki.2012.63. Epub 2012 Mar 28. Kidney Int. 2012. PMID: 22456601 Free article.

9

Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults.

Fremeaux-Bacchi V, Fakhouri F, Garnier A, Bienaimé F, Dragon-Durey MA, Ngo S, Moulin B, Servais A, Provot F, Rostaing L, Burtey S, Niaudet P, Deschênes G, Lebranchu Y, Zuber J, Loirat C. Fremeaux-Bacchi V, et al. Clin J Am Soc Nephrol. 2013 Apr;8(4):554-62. doi: 10.2215/CJN.04760512. Epub 2013 Jan 10. Clin J Am Soc Nephrol. 2013. PMID: 23307876 Free PMC article.

10

The authors reply:

Servais A, Noel LH, Lesavre P, Frémeaux-Bacchi V. Servais A, et al. Kidney Int. 2013 Feb;83(2):332-3. doi: 10.1038/ki.2012.381. Kidney Int. 2013. PMID: 23364592 Free article. No abstract available.

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