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

Year Number of Results
2010 3
2011 3
2012 3
2013 1
2014 5
2015 8
2016 5
2017 3
2018 1
2020 7
2021 13
2022 4
2023 5
2024 1

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53 results

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Page 1
Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review.
Kraoua I, Bouyacoub Y, Drissi C, Chargui M, Rebai I, Chebil A, Klaa H, Benrhouma H, Hassen A, Gouider-Khouja N, Abdelhak S, Boespflug-Tanguy O, Youssef-Turki IB, Dorboz I. Kraoua I, et al. Among authors: chebil a. Neuropediatrics. 2021 Aug;52(4):302-309. doi: 10.1055/s-0041-1728654. Epub 2021 Jun 30. Neuropediatrics. 2021. PMID: 34192786 Review.
Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies.
Habibi I, Falfoul Y, Tran HV, El Matri K, Chebil A, El Matri L, Schorderet DF. Habibi I, et al. Among authors: chebil a. Front Cell Dev Biol. 2021 Feb 5;9:625560. doi: 10.3389/fcell.2021.625560. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33634125 Free PMC article.
Genetic spectrum of retinal dystrophies in Tunisia.
Habibi I, Falfoul Y, Turki A, Hassairi A, El Matri K, Chebil A, Schorderet DF, El Matri L. Habibi I, et al. Among authors: chebil a. Sci Rep. 2020 Jul 8;10(1):11199. doi: 10.1038/s41598-020-67792-y. Sci Rep. 2020. PMID: 32641690 Free PMC article.
Choroidal features in non-neovascular and neovascular pachychoroid diseases.
Hachicha I, Bouraoui R, El Matri L, Masmoudi M, Ben Aoun S, Bouchoucha S, Chebil A, Limaiem R, El Matri K. Hachicha I, et al. Among authors: chebil a. Eur J Ophthalmol. 2023 Nov 1:11206721231210755. doi: 10.1177/11206721231210755. Online ahead of print. Eur J Ophthalmol. 2023. PMID: 37915116
53 results