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Page 1
A FOXG1 mutation in a boy with congenital variant of Rett syndrome.
Le Guen T, Bahi-Buisson N, Nectoux J, Boddaert N, Fichou Y, Diebold B, Desguerre I, Raqbi F, Daire VC, Chelly J, Bienvenu T. Le Guen T, et al. Among authors: raqbi f. Neurogenetics. 2011 Feb;12(1):1-8. doi: 10.1007/s10048-010-0255-4. Epub 2010 Aug 24. Neurogenetics. 2011. PMID: 20734096 Review.
[Cases of imported cholera in France, summer 2005. A. Tarantola for the incident management teams].
Groupes de Gestion des Incidents, Ajzenman C, Bizet MC, Dufraisse MP, Falip E, Fournier JM, Etchegorry MG, Haeghebaert S, Isnard H, Le Loc'h H, Mansir T, Quilici ML, Raqbi F, Raud E, Roberto Y, Scanvic A, Senellier M, Sirot S, Tarantola A. Groupes de Gestion des Incidents, et al. Among authors: raqbi f. Med Mal Infect. 2006 Jun;36(6):346-8. doi: 10.1016/j.medmal.2006.01.012. Epub 2006 Jun 27. Med Mal Infect. 2006. PMID: 16806780 French.
[Radiologic case of the month].
Anjot MN, Raqbi F, Abadie V, Desguerre I. Anjot MN, et al. Among authors: raqbi f. Arch Pediatr. 2001 Sep;8(9):987-9. doi: 10.1016/s0929-693x(01)00566-8. Arch Pediatr. 2001. PMID: 11582942 French. No abstract available.