Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

49 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
[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: ben dridi mf. 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: ben chehida a, ben dridi mf. 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.
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: ben turkia h, ben dridi mf. 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
[Rosai-Dorfman disease: therapeutic issues in 2 cases].
Ben Turkia H, Ben Romdhane M, Azzouz H, Ben Chehida A, Slim Abdelmoula M, Benabdelaziz R, Tebib N, Ben Messaoud M, Sahtout S, Chelly I, Zitouna M, Mnif E, Ben Dridi MF. Ben Turkia H, et al. Among authors: ben romdhane m, ben messaoud m, ben chehida a, ben dridi mf. Arch Pediatr. 2011 Nov;18(11):1205-9. doi: 10.1016/j.arcped.2011.08.008. Epub 2011 Oct 12. Arch Pediatr. 2011. PMID: 21992893 French.
[Inborn metabolic disorders in Tunisia: challenges, experience and hopes].
Ben Dridi MF, Ben Turkia H, Azzouz H, Ben Chehida A, Ben Abdelaziz R, Tebib N. Ben Dridi MF, et al. Among authors: ben abdelaziz r, ben turkia h, ben chehida a. Arch Pediatr. 2015 May;22(5 Suppl 1):3-4. doi: 10.1016/S0929-693X(15)30003-8. Arch Pediatr. 2015. PMID: 26112494 French. No abstract available.
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: ben turkia h, ben chehida a, ben dridi mf, ben rhouma f. 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: ben dridi mf. 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
[Renal involvement in Fabry disease].
Kaaroud H, Béji S, Boubaker K, Ben Moussa F, Ben Hamida F, Goucha R, Ben Dridi MF, Ben Turkia H, Kheder A. Kaaroud H, et al. Among authors: ben moussa f, ben hamida f, ben turkia h, ben dridi mf. Tunis Med. 2007 Mar;85(3):240-3. Tunis Med. 2007. PMID: 17668583 French.
49 results