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Page 1
[Richner-Hanhart syndrome].
Zribi H, Souissi A, Azzouz H, Tebib N, Mokni M. Zribi H, et al. Among authors: tebib n. Presse Med. 2016 Feb;45(2):264-5. doi: 10.1016/j.lpm.2015.03.016. Epub 2016 Feb 12. Presse Med. 2016. PMID: 26880079 French. No abstract available.
A case of a Tunisian Rett patient with a novel double-mutation of the MECP2 gene.
Fendri-Kriaa N, Hsairi I, Kifagi C, Ellouze E, Mkaouar-Rebai E, Triki C, Fakhfakh F; Tunisian network on mental retardation study. Fendri-Kriaa N, et al. Biochem Biophys Res Commun. 2011 Jun 3;409(2):270-4. doi: 10.1016/j.bbrc.2011.04.140. Epub 2011 May 7. Biochem Biophys Res Commun. 2011. PMID: 21575601
Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutations.
Charfeddine C, Monastiri K, Mokni M, Laadjimi A, Kaabachi N, Perin O, Nilges M, Kassar S, Keirallah M, Guediche MN, Kamoun MR, Tebib N, Ben Dridi MF, Boubaker S, Ben Osman A, Abdelhak S. Charfeddine C, et al. Among authors: tebib n. Mol Genet Metab. 2006 Jun;88(2):184-91. doi: 10.1016/j.ymgme.2006.02.006. Epub 2006 Mar 30. Mol Genet Metab. 2006. PMID: 16574453
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: tebib n. 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
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: tebib n. 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
Glycogen storage disease type I in Tunisia: an epidemiological analysis.
Ben Chehida A, Tebib N, Cherif W, Ben Turkia H, Abdelmoula S, Azzouz H, Ben Dridi MF. Ben Chehida A, et al. Among authors: tebib n. J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S199-204. doi: 10.1007/s10545-008-0707-2. Epub 2008 Aug 5. J Inherit Metab Dis. 2008. PMID: 18679824
[Atypical presentation of Wegener disease in childhood].
Ben Turkia H, Amdouni N, Azzouz H, Tebib N, Abdelmoula MS, El Mazni F, Hamzaoui A, Ben Dridi MF. Ben Turkia H, et al. Among authors: tebib n. J Mal Vasc. 2008 Dec;33(4-5):242-6. doi: 10.1016/j.jmv.2008.09.007. Epub 2008 Nov 20. J Mal Vasc. 2008. PMID: 19022597 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: tebib n. 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.
97 results