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[Molecular diagnosis of Gaucher disease in Tunisia].
Cherif W, Ben Turkia H, Ben Rhouma F, Riahi I, Chemli J, Amaral O, Sá Miranda MC, Caillaud C, Kaabachi N, Tebib N, Abdelhak S, Ben Dridi MF. Cherif W, et al. Among authors: caillaud c. Pathol Biol (Paris). 2013 Apr;61(2):59-63. doi: 10.1016/j.patbio.2012.03.006. Epub 2012 Apr 27. Pathol Biol (Paris). 2013. PMID: 22542428 French.
Gaucher disease in Tunisia: High frequency of the most common mutations.
Cherif W, Ben Turkia H, Ben Rhouma F, Riahi I, Chemli J, Kefi R, Messai H, Amaral O, Miranda MC, Caillaud C, Tebib N, Ben Dridi MF, Abdelhak S. Cherif W, et al. Among authors: caillaud c. Blood Cells Mol Dis. 2009 Sep-Oct;43(2):161-2. doi: 10.1016/j.bcmd.2009.05.004. Epub 2009 Jun 23. Blood Cells Mol Dis. 2009. PMID: 19553144 No abstract available.
Phenotypic spectrum of fucosidosis in Tunisia.
Ben Turkia H, Tebib N, Azzouz H, Abdelmoula MS, Bouguila J, Sanhaji H, Miladi N, Maire I, Caillaud C, Kaabachi N, Ben Dridi MF. Ben Turkia H, et al. Among authors: caillaud c. J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S313-6. doi: 10.1007/s10545-008-0891-0. Epub 2008 Jul 27. J Inherit Metab Dis. 2008. PMID: 18651239
[Neonatal cholestasis in an intermediate phenotype of type 2 Gaucher disease].
Ben Turkia H, Tebib N, Kasdallah N, Abdelmoula MS, Azzouz H, Ben Chehida A, Caillaud C, Ben Dridi MF. Ben Turkia H, et al. Among authors: caillaud c. Arch Pediatr. 2009 Mar;16(3):255-7. doi: 10.1016/j.arcped.2008.11.019. Epub 2009 Jan 31. Arch Pediatr. 2009. PMID: 19181499 French. No abstract available.
264 results