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

54 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
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: cherif w. 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
[Molecular diagnosis of Gaucher disease in Tunisia].
Cherif W, Ben Turkia H, Ben Rhouma F, Riahi I, Chemli J, Amaral O, Sá Miranda MC, Caillaud C, Kaabachi N, Tebib N, Abdelhak S, Ben Dridi MF. Cherif W, et al. Pathol Biol (Paris). 2013 Apr;61(2):59-63. doi: 10.1016/j.patbio.2012.03.006. Epub 2012 Apr 27. Pathol Biol (Paris). 2013. PMID: 22542428 French.
Gaucher disease in Tunisia: High frequency of the most common mutations.
Cherif W, Ben Turkia H, Ben Rhouma F, Riahi I, Chemli J, Kefi R, Messai H, Amaral O, Miranda MC, Caillaud C, Tebib N, Ben Dridi MF, Abdelhak S. Cherif W, et al. Blood Cells Mol Dis. 2009 Sep-Oct;43(2):161-2. doi: 10.1016/j.bcmd.2009.05.004. Epub 2009 Jun 23. Blood Cells Mol Dis. 2009. PMID: 19553144 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: cherif w. Tunis Med. 2010 Mar;88(3):158-62. Tunis Med. 2010. PMID: 20415187 Free article. French.
Adult Gaucher disease in southern Tunisia: report of three cases.
Ben Rhouma F, Kallel F, Kefi R, Cherif W, Nagara M, Azaiez H, Jedidi I, Elloumi M, Abdelhak S, Mseddi S. Ben Rhouma F, et al. Among authors: cherif w. Diagn Pathol. 2012 Jan 10;7:4. doi: 10.1186/1746-1596-7-4. Diagn Pathol. 2012. PMID: 22233685 Free PMC article.
Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia.
Ben Halim N, Hsouna S, Lasram K, Rejeb I, Walha A, Talmoudi F, Messai H, Sabrine Ben Brick A, Ouragini H, Cherif W, Nagara M, Ben Rhouma F, Chouchene I, Ouechtati F, Bouyacoub Y, Ben Rekaya M, Messaoud O, Ben Ammar S, El Matri L, Tebib N, Ben Dridi MF, Mokni M, Amouri A, Kefi R, Abdelhak S. Ben Halim N, et al. Among authors: cherif w. Am J Hum Biol. 2016 Mar-Apr;28(2):171-80. doi: 10.1002/ajhb.22764. Epub 2015 Jul 16. Am J Hum Biol. 2016. PMID: 26179682
History of settlement of villages from Central Tunisia by studying families sharing a common founder Glycogenosis type III mutation.
Rhouma FB, Messai H, Hsouna S, Halim NB, Cherif W, Fadhel SB, Tiar A, Nagara M, Azzouz H, Sfar MT, Dridi MF, Tebib N, Ayadi A, Abdelhak S, Kefi R. Rhouma FB, et al. Among authors: cherif w. Mitochondrial DNA A DNA Mapp Seq Anal. 2016 Sep;27(5):3194-8. doi: 10.3109/19401736.2015.1007331. Epub 2015 Dec 24. Mitochondrial DNA A DNA Mapp Seq Anal. 2016. PMID: 26704523
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: cherif w. 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
54 results