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Page 1
Optical Coherence Tomographic Findings in Berlin's Edema.
El Matri L, Chebil A, Kort F, Bouraoui R, Largueche L, Mghaieth F. El Matri L, et al. Among authors: largueche l. J Ophthalmic Vis Res. 2010 Apr;5(2):127-9. J Ophthalmic Vis Res. 2010. PMID: 22737342 Free PMC article.
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: largueche 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
Choroidal thickness measurement in highly myopic eyes using SD-OCT.
El Matri L, Bouladi M, Chebil A, Kort F, Bouraoui R, Largueche L, Mghaieth F. El Matri L, et al. Among authors: largueche l. Ophthalmic Surg Lasers Imaging. 2012 Nov-Dec;43(6 Suppl):S38-43. doi: 10.3928/15428877-20121001-02. Ophthalmic Surg Lasers Imaging. 2012. PMID: 23357323
Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients.
Riahi Z, Bonnet C, Zainine R, Lahbib S, Bouyacoub Y, Bechraoui R, Marrakchi J, Hardelin JP, Louha M, Largueche L, Ben Yahia S, Kheirallah M, Elmatri L, Besbes G, Abdelhak S, Petit C. Riahi Z, et al. Among authors: largueche l. PLoS One. 2015 Mar 23;10(3):e0120584. doi: 10.1371/journal.pone.0120584. eCollection 2015. PLoS One. 2015. PMID: 25798947 Free PMC article.
16 results