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Custom Next-Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneys.
Said MB, Ayed IB, Elloumi I, Hasnaoui M, Souissi A, Idriss N, Aloulou H, Chabchoub I, Maâlej B, Driss D, Masmoudi S. Said MB, et al. Mol Genet Genomic Med. 2022 Feb;10(2):e1868. doi: 10.1002/mgg3.1868. Epub 2022 Jan 8. Mol Genet Genomic Med. 2022. PMID: 34997822 Free PMC article.
Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locus.
Belguith H, Aifa-Hmani M, Dhouib H, Said MB, Mosrati MA, Lahmar I, Moalla J, Charfeddine I, Driss N, Arab SB, Ghorbel A, Ayadi H, Masmoudi S. Belguith H, et al. Among authors: said mb. Genet Test Mol Biomarkers. 2009 Feb;13(1):147-51. doi: 10.1089/gtmb.2008.0077. Genet Test Mol Biomarkers. 2009. PMID: 19309289
The incidence and prevalence of serious fungal diseases in Tunisia.
Fathallah A, Chouaieb H, Saief MB, Ismaïl S, Said MB, Denning DW; in association with the Tunisian Society for Infectious Diseases (Société Tunisienne de Pathologie Infectieuse (STPI)). Fathallah A, et al. Among authors: said mb. J Mycol Med. 2024 Apr 5;34(2):101479. doi: 10.1016/j.mycmed.2024.101479. Online ahead of print. J Mycol Med. 2024. PMID: 38604083 Free article. Review.
32 results