Salomon R - Search Results

1

Association between 25(OH) vitamin D and graft survival in renal transplanted children.

Mosca M, Lion-Lambert M, Bienaimé F, Berthaud R, Dorval G, Garcelon N, Dehoux L, Krid S, Charbit M, Rabant M, Niaudet P, Salomon R, Bacchetta J, Boyer O. Mosca M, et al. Among authors: salomon r. Pediatr Transplant. 2020 Nov;24(7):e13809. doi: 10.1111/petr.13809. Epub 2020 Aug 26. Pediatr Transplant. 2020. PMID: 32845557

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

[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.

5

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

6

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.

7

[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.

8

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

9

Prognosis of autosomal dominant polycystic kidney disease diagnosed in utero or at birth.

Boyer O, Gagnadoux MF, Guest G, Biebuyck N, Charbit M, Salomon R, Niaudet P. Boyer O, et al. Among authors: salomon r. Pediatr Nephrol. 2007 Mar;22(3):380-8. doi: 10.1007/s00467-006-0327-8. Epub 2006 Nov 24. Pediatr Nephrol. 2007. PMID: 17124604

10

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

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