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[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: abdelmoula ms. 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.
[Phenotype and mutational spectrum in Tunisian pediatric gaucher disease].
Ben Turkia H, Riahi I, Azzouz H, Ladab S, Cherif W, Ben Chehida A, Abdelmoula MS, Caillaud C, Chemli J, Abdelhak S, Tebib N, Ben Dridi MF. Ben Turkia H, et al. Among authors: abdelmoula ms. Tunis Med. 2010 Mar;88(3):158-62. Tunis Med. 2010. PMID: 20415187 Free article. French.
Congenital hyperinsulinism: review of 12 Tunisian cases.
Ben Turkia H, Brahim K, Azzouz H, Tebib N, Abdelmoula MS, Ben Chehida A, Fekih M, Sayed S, Kaabar N, Francoise Ben Dridi M. Ben Turkia H, et al. Among authors: abdelmoula ms. Tunis Med. 2011 Apr;89(4):369-73. Tunis Med. 2011. PMID: 21484688 Free article.
[Rosai -Dorfman disease: a two cases report].
Ben Turkia H, Ben Romdhane M, Azzouz H, Ben Chehida A, Abdelmoula MS, Ben Abdelaziz R, Tebib N, Ben Messoud M, Sahtout S, Chelly I, Zitouni M, Mnif E, Ben Dridi MF. Ben Turkia H, et al. Among authors: abdelmoula ms. Tunis Med. 2011 May;89(5):497-501. Tunis Med. 2011. PMID: 21557191 Free article. French.
26 results