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Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene.
Ouechtati F, Merdassi A, Bouyacoub Y, Largueche L, Derouiche K, Ouragini H, Nouira S, Tiab L, Baklouti K, Rebai A, Schorderet DF, Munier FL, Zografos L, Abdelhak S, El Matri L. Ouechtati F, et al. Among authors: el matri l. J Hum Genet. 2011 Jan;56(1):22-8. doi: 10.1038/jhg.2010.128. Epub 2010 Nov 25. J Hum Genet. 2011. PMID: 21107338
Pediatric penetrating keratoplasty: indications and outcomes.
Limaiem R, Chebil A, Baba A, Ben Youssef N, Mghaieth F, El Matri L. Limaiem R, et al. Among authors: el matri l. Transplant Proc. 2011 Mar;43(2):649-51. doi: 10.1016/j.transproceed.2011.01.055. Transplant Proc. 2011. PMID: 21440785
[Epidemiologic study of pediatric uveitis: a series of 49 cases].
Chebil A, Chaabani L, Kort F, Ben Youssef N, Turki F, El Matri L. Chebil A, et al. Among authors: el matri l. J Fr Ophtalmol. 2012 Jan;35(1):30-4. doi: 10.1016/j.jfo.2011.02.019. Epub 2011 Sep 1. J Fr Ophtalmol. 2012. PMID: 21889818 French.
162 results