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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2005 2
2006 1
2007 2
2008 3
2010 3
2011 1
2012 2
2013 3
2014 1
2015 1
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2017 4
2018 2
2019 3
2020 4
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2023 5
2024 5

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Page 1
Mitochondrial mutations in non-syndromic hearing loss at UAE.
Mohamed WKE, Arnoux M, Cardoso THS, Almutery A, Tlili A. Mohamed WKE, et al. Among authors: tlili a. Int J Pediatr Otorhinolaryngol. 2020 Nov;138:110286. doi: 10.1016/j.ijporl.2020.110286. Epub 2020 Aug 7. Int J Pediatr Otorhinolaryngol. 2020. PMID: 32871514
Identification of a novel homozygous mutation in NAXE gene associated with early-onset progressive encephalopathy by whole-exome sequencing: in silico protein structure characterization, molecular docking, and dynamic simulation.
Maalej M, Sfaihi L, Ammar M, Frikha F, Kharrat M, Alila-Fersi O, Mkaouar-Rebai E, Tlili A, Kammoun T, Fakhfakh F. Maalej M, et al. Among authors: tlili a. Neurogenetics. 2022 Oct;23(4):257-270. doi: 10.1007/s10048-022-00696-3. Epub 2022 Jul 11. Neurogenetics. 2022. PMID: 35819538
Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome.
Dulon D, Papal S, Patni P, Cortese M, Vincent PF, Tertrais M, Emptoz A, Tlili A, Bouleau Y, Michel V, Delmaghani S, Aghaie A, Pepermans E, Alegria-Prevot O, Akil O, Lustig L, Avan P, Safieddine S, Petit C, El-Amraoui A. Dulon D, et al. Among authors: tlili a. J Clin Invest. 2018 Aug 1;128(8):3382-3401. doi: 10.1172/JCI94351. Epub 2018 Jul 9. J Clin Invest. 2018. PMID: 29985171 Free PMC article.
53 results