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Global sequencing approach for characterizing the molecular background of hereditary iron disorders.
Cunat S, Giansily-Blaizot M, Bismuth M, Blanc F, Dereure O, Larrey D, Quellec AL, Pouderoux P, Rose C, Raingeard I, Renard E, Schved JF, Aguilar-Martinez P; CHU Montpellier AOI 2004 Working Group. Cunat S, et al. Among authors: dereure o. Clin Chem. 2007 Dec;53(12):2060-9. doi: 10.1373/clinchem.2007.090605. Epub 2007 Oct 19. Clin Chem. 2007. PMID: 17951290
The Southern French registry of genetic hemochromatosis: a tool for determining clinical prevalence of the disorder and genotype penetrance.
Aguilar-Martinez P, Bismuth M, Blanc F, Blanc P, Cunat S, Dereure O, Dujols P, Giansily-Blaizot M, Jorgensen C, Konate A, Larrey D, Le Quellec A, Mura T, Raingeard I, Ramos J, Renard E, Rousseau F, Schved JF, Picot MC. Aguilar-Martinez P, et al. Among authors: dereure o. Haematologica. 2010 Apr;95(4):551-6. doi: 10.3324/haematol.2009.014431. Epub 2010 Feb 9. Haematologica. 2010. PMID: 20145272 Free PMC article.
Porphyria cutanea tarda and spherocytosis: a non-random association?
Du-Thanh A, Aguilar-Martinez P, Enescu C, Cunat S, Guillot B, Dereure O. Du-Thanh A, et al. Among authors: dereure o. Acta Derm Venereol. 2013 May;93(3):377-8. doi: 10.2340/00015555-1493. Acta Derm Venereol. 2013. PMID: 23093332 Free article. No abstract available.
509 results