Salomon R - Search Results

1

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. Among authors: salomon r. 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

2

Genetics of the nephrotic syndrome.

Salomon R, Gubler MC, Niaudet P. Salomon R, et al. Curr Opin Pediatr. 2000 Apr;12(2):129-34. doi: 10.1097/00008480-200004000-00008. Curr Opin Pediatr. 2000. PMID: 10763762 Review.

3

Hemolytic-uremic syndrome: hereditary forms and forms associated with hereditary diseases.

Niaudet P, Gagnadoux MF, Broyer M, Salomon R. Niaudet P, et al. Among authors: salomon r. Adv Nephrol Necker Hosp. 2000;30:261-80. Adv Nephrol Necker Hosp. 2000. PMID: 11068647 Review. No abstract available.

4

PAX2 mutations in oligomeganephronia.

Salomon R, Tellier AL, Attie-Bitach T, Amiel J, Vekemans M, Lyonnet S, Dureau P, Niaudet P, Gubler MC, Broyer M. Salomon R, et al. Kidney Int. 2001 Feb;59(2):457-62. doi: 10.1046/j.1523-1755.2001.059002457.x. Kidney Int. 2001. PMID: 11168927 Free article.

5

[Analgesia with oxygen-nitrous oxide mixture during percutaneous renal biopsy in children].

Piétrement C, Salomon R, Monceaux F, Petitjean C, Niaudet P. Piétrement C, et al. Among authors: salomon r. Arch Pediatr. 2001 Feb;8(2):145-9. doi: 10.1016/s0929-693x(00)00176-7. Arch Pediatr. 2001. PMID: 11232454 Clinical Trial. French.

6

High serum levels of a non-(1-84) parathyroid hormone (PTH) fragment in pediatric haemodialysis patients.

Salomon R, Charbit M, Gagnadoux MF, Niaudet P, Gao P, Cantor T, Souberbielle JC. Salomon R, et al. Pediatr Nephrol. 2001 Dec;16(12):1011-4. doi: 10.1007/s004670100014. Pediatr Nephrol. 2001. PMID: 11793090

7

Intravenous cyclosporine therapy in recurrent nephrotic syndrome after renal transplantation in children.

Salomon R, Gagnadoux MF, Niaudet P. Salomon R, et al. Transplantation. 2003 Mar 27;75(6):810-4. doi: 10.1097/01.TP.0000055215.20367.21. Transplantation. 2003. PMID: 12660507 Clinical Trial.

8

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: salomon r. 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.

9

[Nephronophtisis].

Niaudet P, Salomon R. Niaudet P, et al. Among authors: salomon r. Nephrol Ther. 2006 Sep;2(4):200-6. doi: 10.1016/j.nephro.2006.06.006. Epub 2006 Aug 1. Nephrol Ther. 2006. PMID: 16966065 Review. French.

10

Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study.

Weber S, Moriniere V, Knüppel T, Charbit M, Dusek J, Ghiggeri GM, Jankauskiené A, Mir S, Montini G, Peco-Antic A, Wühl E, Zurowska AM, Mehls O, Antignac C, Schaefer F, Salomon R. Weber S, et al. Among authors: salomon r. J Am Soc Nephrol. 2006 Oct;17(10):2864-70. doi: 10.1681/ASN.2006030277. Epub 2006 Sep 13. J Am Soc Nephrol. 2006. PMID: 16971658

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