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Page 1
Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosis.
Barkaoui E, Cherif W, Tebib N, Charfeddine C, Ben Rhouma F, Azzouz H, Ben Chehida A, Monastiri K, Chemli J, Amri F, Ben Turkia H, Abdelmoula MS, Kaabachi N, Abdelhak S, Ben Dridi MF. Barkaoui E, et al. Among authors: abdelmoula ms. J Inherit Metab Dis. 2007 Nov;30(6):989. doi: 10.1007/s10545-007-0737-1. Epub 2007 Nov 19. J Inherit Metab Dis. 2007. PMID: 18008183
Incidence of mucopolysaccharidoses in Tunisia.
Ben Turkia H, Tebib N, Azzouz H, Abdelmoula MS, Ben Chehida A, Chemli J, Monastiri K, Chaabouni M, Sanhagi H, Zouari B, Kaabachi N, Ben Dridi MF. Ben Turkia H, et al. Among authors: abdelmoula ms. Tunis Med. 2009 Nov;87(11):782-5. Tunis Med. 2009. PMID: 20209839 Free article.
[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.
[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.
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: abdelmoula ms. 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
26 results