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Urine in clinical proteomics.
Decramer S, Gonzalez de Peredo A, Breuil B, Mischak H, Monsarrat B, Bascands JL, Schanstra JP. Decramer S, et al. Mol Cell Proteomics. 2008 Oct;7(10):1850-62. doi: 10.1074/mcp.R800001-MCP200. Epub 2008 Jul 30. Mol Cell Proteomics. 2008. PMID: 18667409 Free article. Review.
[Berger's disease in childhood].
Decramer S. Decramer S. Arch Pediatr. 2002 May;9(5):519-29. doi: 10.1016/s0929-693x(01)00836-3. Arch Pediatr. 2002. PMID: 12053548 Review. French.
Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.
Legrand A, Treard C, Roncelin I, Dreux S, Bertholet-Thomas A, Broux F, Bruno D, Decramer S, Deschenes G, Djeddi D, Guigonis V, Jay N, Khalifeh T, Llanas B, Morin D, Morin G, Nobili F, Pietrement C, Ryckewaert A, Salomon R, Vrillon I, Blanchard A, Vargas-Poussou R. Legrand A, et al. Among authors: decramer s. Clin J Am Soc Nephrol. 2018 Feb 7;13(2):242-250. doi: 10.2215/CJN.05670517. Epub 2017 Nov 16. Clin J Am Soc Nephrol. 2018. PMID: 29146702 Free PMC article.
The HNF1B score is a simple tool to select patients for HNF1B gene analysis.
Faguer S, Chassaing N, Bandin F, Prouheze C, Garnier A, Casemayou A, Huart A, Schanstra JP, Calvas P, Decramer S, Chauveau D. Faguer S, et al. Among authors: decramer s. Kidney Int. 2014 Nov;86(5):1007-15. doi: 10.1038/ki.2014.202. Epub 2014 Jun 4. Kidney Int. 2014. PMID: 24897035 Free article. Review.
137 results