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

167 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
CDH23 Methylation Status and Presbycusis Risk in Elderly Women.
Bouzid A, Smeti I, Chakroun A, Loukil S, Gibriel AA, Grati M, Ghorbel A, Masmoudi S. Bouzid A, et al. Among authors: masmoudi s. Front Aging Neurosci. 2018 Aug 7;10:241. doi: 10.3389/fnagi.2018.00241. eCollection 2018. Front Aging Neurosci. 2018. PMID: 30131691 Free PMC article.
Identification of candidate regions for a novel Usher syndrome type II locus.
Ben Rebeh I, Benzina Z, Dhouib H, Hadjamor I, Amyere M, Ayadi L, Turki K, Hammami B, Kmiha N, Kammoun H, Hakim B, Charfedine I, Vikkula M, Ghorbel A, Ayadi H, Masmoudi S. Ben Rebeh I, et al. Among authors: masmoudi s. Mol Vis. 2008 Sep 19;14:1719-26. Mol Vis. 2008. PMID: 18806881 Free PMC article.
Mutation in gap and tight junctions in patients with non-syndromic hearing loss.
Belguith H, Tlili A, Dhouib H, Ben Rebeh I, Lahmar I, Charfeddine I, Driss N, Ghorbel A, Ayadi H, Masmoudi S. Belguith H, et al. Among authors: masmoudi s. Biochem Biophys Res Commun. 2009 Jul 17;385(1):1-5. doi: 10.1016/j.bbrc.2009.02.125. Epub 2009 Feb 28. Biochem Biophys Res Commun. 2009. PMID: 19254696
High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effects.
Ben Saïd M, Hmani-Aifa M, Amar I, Baig SM, Mustapha M, Delmaghani S, Tlili A, Ghorbel A, Ayadi H, Van Camp G, Smith RJ, Tekin M, Masmoudi S. Ben Saïd M, et al. Among authors: masmoudi s. Genet Test Mol Biomarkers. 2010 Jun;14(3):307-11. doi: 10.1089/gtmb.2009.0174. Genet Test Mol Biomarkers. 2010. PMID: 20373850 Free PMC article.
Pendred syndrome in Tunisia.
Charfeddine I, Mnejja M, Hammami B, Chakroun A, Masmoudi S, Ayadi H, Ghorbel A. Charfeddine I, et al. Among authors: masmoudi s. Eur Ann Otorhinolaryngol Head Neck Dis. 2010 Mar;127(1):7-10. doi: 10.1016/j.anorl.2010.02.002. Epub 2010 Mar 24. Eur Ann Otorhinolaryngol Head Neck Dis. 2010. PMID: 20822748 Free article.
A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family.
Ben Saïd M, Ayedi L, Mnejja M, Hakim B, Khalfallah A, Charfeddine I, Khifagi C, Turki K, Ayadi H, Benzina Z, Ghorbel A, Castillo ID, Masmoudi S, Aifa MH. Ben Saïd M, et al. Among authors: masmoudi s. Eur J Med Genet. 2011 Nov-Dec;54(6):e535-41. doi: 10.1016/j.ejmg.2011.06.008. Epub 2011 Jul 13. Eur J Med Genet. 2011. PMID: 21802533
167 results