Tebib N - Search Results

1

Phenylketonuria is still a major cause of mental retardation in Tunisia despite the possibility of treatment.

Khemir S, El Asmi M, Sanhaji H, Feki M, Jemaa R, Tebib N, Dhondt JL, Ben Dridi MF, Mebazaa A, Kaabachi N. Khemir S, et al. Among authors: tebib n. Clin Neurol Neurosurg. 2011 Nov;113(9):727-30. doi: 10.1016/j.clineuro.2011.07.016. Epub 2011 Sep 8. Clin Neurol Neurosurg. 2011. PMID: 21862209

2

[Pompe's disease: a report of 3 cases (clinical, biochemical, anatomo-pathological study].

Ben Dridi MF, Samoud A, Tebib N, Slim M, Taktak M, Hentati F, Boubaker S. Ben Dridi MF, et al. Among authors: tebib n. Tunis Med. 1990 Jun-Jul;68(6-7):463-7. Tunis Med. 1990. PMID: 2238143 French. No abstract available.

3

[The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders].

Khiari D, Tebib N, Kaabachi N, Ben Dridi MF, Mebazaa A. Khiari D, et al. Among authors: tebib n. Tunis Med. 1995 May;73(5):159-67. Tunis Med. 1995. PMID: 9507277 Review. French. No abstract available.

4

[Reference values of urinary orotic acid in a healthy Tunisian population].

el Khiari D, Tebib N, Kaabachi N, Feki M, Ben Hamouda Y, Mebazaa A. el Khiari D, et al. Among authors: tebib n. Arch Pediatr. 1998 Jan;5(1):15-8. doi: 10.1016/s0929-693x(97)83460-4. Arch Pediatr. 1998. PMID: 10223105 French.

5

[Visceral leishmaniasis in children: prognostic factors].

Abdelmoula MS, M'Hamdi Z, Amri F, Tebib N, Ben Turkia H, Ben Dridi MF. Abdelmoula MS, et al. Among authors: tebib n. Tunis Med. 2003 Aug;81(8):535-9. Tunis Med. 2003. PMID: 14608735 French.

6

[Gaucher's disease in Tunisia (multicenter study)].

Chaabouni M, Aoulou H, Tebib N, Hachicha M, Ben Becher S, Monastiri K, Yacoub M, Sfar T, Elloumi M, Chakroun N, Miled M, Ben Dridi MF. Chaabouni M, et al. Among authors: tebib n. Rev Med Interne. 2004 Feb;25(2):104-10. doi: 10.1016/s0248-8663(03)00267-4. Rev Med Interne. 2004. PMID: 14744639 French.

7

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

8

[Pulmonary aspergillosis in a child with chronic granulomatous disease].

Abdelmoula MS, Abdelmalek R, Chleyfa K, Bejaoui M, Tebib N, Ben Turkia H, Ben Dridi MF. Abdelmoula MS, et al. Among authors: tebib n. Tunis Med. 2003 Oct;81(10):815-20. Tunis Med. 2003. PMID: 17722799 French.

9

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

10

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

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