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

Year Number of Results
2002 2
2003 5
2004 3
2005 7
2007 1
2008 1
2009 1
2010 2
2011 1
2012 3
2013 3
2014 3
2016 3
2017 4
2018 2
2019 1
2020 3
2021 3
2022 3
2024 1

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49 results

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Page 1
Clarin-2 gene supplementation durably preserves hearing in a model of progressive hearing loss.
Mendia C, Peineau T, Zamani M, Felgerolle C, Yahiaoui N, Christophersen N, Papal S, Maudoux A, Maroofian R, Patni P, Nouaille S, Bowl MR, Delmaghani S, Galehdari H, Vona B, Dulon D, Vitry S, El-Amraoui A. Mendia C, et al. Among authors: el amraoui a. Mol Ther. 2024 Mar 6;32(3):800-817. doi: 10.1016/j.ymthe.2024.01.021. Epub 2024 Jan 18. Mol Ther. 2024. PMID: 38243601 Free article.
Review of Genotype-Phenotype Correlations in Usher Syndrome.
Nisenbaum E, Thielhelm TP, Nourbakhsh A, Yan D, Blanton SH, Shu Y, Koehler KR, El-Amraoui A, Chen Z, Lam BL, Liu X. Nisenbaum E, et al. Among authors: el amraoui a. Ear Hear. 2022 Jan/Feb;43(1):1-8. doi: 10.1097/AUD.0000000000001066. Ear Hear. 2022. PMID: 34039936 Free PMC article. Review.
Stem Cells and Gene Therapy in Progressive Hearing Loss: the State of the Art.
Nourbakhsh A, Colbert BM, Nisenbaum E, El-Amraoui A, Dykxhoorn DM, Koehler KR, Chen ZY, Liu XZ. Nourbakhsh A, et al. Among authors: el amraoui a. J Assoc Res Otolaryngol. 2021 Apr;22(2):95-105. doi: 10.1007/s10162-020-00781-0. Epub 2021 Jan 28. J Assoc Res Otolaryngol. 2021. PMID: 33507440 Free PMC article. Review.
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans.
Vona B, Mazaheri N, Lin SJ, Dunbar LA, Maroofian R, Azaiez H, Booth KT, Vitry S, Rad A, Rüschendorf F, Varshney P, Fowler B, Beetz C, Alagramam KN, Murphy D, Shariati G, Sedaghat A, Houlden H, Petree C, VijayKumar S, Smith RJH, Haaf T, El-Amraoui A, Bowl MR, Varshney GK, Galehdari H. Vona B, et al. Among authors: el amraoui a. Hum Genet. 2021 Jun;140(6):915-931. doi: 10.1007/s00439-020-02254-z. Epub 2021 Jan 26. Hum Genet. 2021. PMID: 33496845 Free PMC article.
Disease mechanisms and gene therapy for Usher syndrome.
Géléoc GGS, El-Amraoui A. Géléoc GGS, et al. Among authors: el amraoui a. Hear Res. 2020 Sep 1;394:107932. doi: 10.1016/j.heares.2020.107932. Epub 2020 Mar 4. Hear Res. 2020. PMID: 32199721 Review.
Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family.
Charfeddine C, Dallali H, Abdessalem G, Ghedira K, Hamdi Y, Elouej S, Landoulsi Z, Delague V, Lagarde A, Levy N, El-Amraoui A, Boubaker MS, Abdelhak S, Mokni M. Charfeddine C, et al. Among authors: el amraoui a. J Hum Genet. 2020 Apr;65(4):397-410. doi: 10.1038/s10038-019-0711-4. Epub 2020 Jan 7. J Hum Genet. 2020. PMID: 31911611 Free article. Clinical Trial.
49 results