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Absent meibomian glands and cone dystrophy in ADULT syndrome: identification by whole exome sequencing of pathogenic variants in two causal genes TP63 and CNGB3.
Hizem S, Maamouri R, Zaouak A, Rejeb I, Karoui S, Sebai M, Jilani H, Elaribi Y, Fenniche S, Cheour M, Bilan F, Ben Jemaa L. Hizem S, et al. Among authors: maamouri r. Ophthalmic Genet. 2024 Feb;45(1):84-94. doi: 10.1080/13816810.2023.2206891. Epub 2023 May 9. Ophthalmic Genet. 2024. PMID: 37158316
[Peripapillary changes detected by SD OCT in eyes in high myopia].
Chebil A, Ben Achour B, Maamouri R, Ben Abdallah M, El Matri L. Chebil A, et al. Among authors: maamouri r. J Fr Ophtalmol. 2014 Oct;37(8):635-9. doi: 10.1016/j.jfo.2014.07.007. Epub 2014 Sep 6. J Fr Ophtalmol. 2014. PMID: 25199484 French.
[Suicidal behaviors in bipolar disorder type 1].
Maamouri R, Ellini S, Znaidi F, Cheour M, Dammak R. Maamouri R, et al. Encephale. 2022 Dec;48(6):632-637. doi: 10.1016/j.encep.2021.06.013. Epub 2021 Oct 13. Encephale. 2022. PMID: 34654568 French.
32 results