Lesavre P - Search Results

1

Cysteamine therapy delays the progression of nephropathic cystinosis in late adolescents and adults.

Brodin-Sartorius A, Tête MJ, Niaudet P, Antignac C, Guest G, Ottolenghi C, Charbit M, Moyse D, Legendre C, Lesavre P, Cochat P, Servais A. Brodin-Sartorius A, et al. Among authors: lesavre p. Kidney Int. 2012 Jan;81(2):179-89. doi: 10.1038/ki.2011.277. Epub 2011 Sep 7. Kidney Int. 2012. PMID: 21900880 Free article.

2

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. Among authors: lesavre p. 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.

3

Steroid-sensitive nephrotic syndrome: from childhood to adulthood.

Fakhouri F, Bocquet N, Taupin P, Presne C, Gagnadoux MF, Landais P, Lesavre P, Chauveau D, Knebelmann B, Broyer M, Grünfeld JP, Niaudet P. Fakhouri F, et al. Among authors: lesavre p. Am J Kidney Dis. 2003 Mar;41(3):550-7. doi: 10.1053/ajkd.2003.50116. Am J Kidney Dis. 2003. PMID: 12612977

4

Nephronophthisis related to homozygous NPHP1 gene deletion as a cause of chronic renal failure in adults.

Bollée G, Fakhouri F, Karras A, Noël LH, Salomon R, Servais A, Lesavre P, Morinière V, Antignac C, Hummel A. Bollée G, et al. Among authors: lesavre p. Nephrol Dial Transplant. 2006 Sep;21(9):2660-3. doi: 10.1093/ndt/gfl348. Epub 2006 Jun 17. Nephrol Dial Transplant. 2006. PMID: 16782989 No abstract available.

5

The authors reply:

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

6

C3 glomerulopathy.

Servais A, Noël LH, Frémeaux-Bacchi V, Lesavre P. Servais A, et al. Among authors: lesavre p. Contrib Nephrol. 2013;181:185-93. doi: 10.1159/000348654. Epub 2013 May 8. Contrib Nephrol. 2013. PMID: 23689580 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. Among authors: lesavre p. 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

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. Among authors: lesavre p. 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.

9

H deficiency in two brothers with atypical dense intramembranous deposit disease.

Levy M, Halbwachs-Mecarelli L, Gubler MC, Kohout G, Bensenouci A, Niaudet P, Hauptmann G, Lesavre P. Levy M, et al. Among authors: lesavre p. Kidney Int. 1986 Dec;30(6):949-56. doi: 10.1038/ki.1986.278. Kidney Int. 1986. PMID: 2950269 Free article.

10

SLE and idiopathic nephrotic syndrome: coincidence or not?

Hertig A, Droz D, Lesavre P, Grünfeld JP, Rieu P. Hertig A, et al. Among authors: lesavre p. Am J Kidney Dis. 2002 Dec;40(6):1179-84. doi: 10.1053/ajkd.2002.36875. Am J Kidney Dis. 2002. PMID: 12460036

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