Leila Largueche

Boulevard 9-Avril
Tunis, 1006, Tunisia

Last Updated: 09/26/2026

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Found 11 publications

Epidemiologic study of myopia in a population of schoolchildren in Tunisia.

Epidemiologic study of myopia in a population of schoolchildren in Tunisia.

Journal: La Tunisie medicale

Published: August 31, 2016

Molecular exploration of the R91W (RPE65 gene) in Tunisian patients with early onset retinal dystrophy and early onset retinitis pigmentosa

Molecular exploration of the R91W (RPE65 gene) in Tunisian patients with early onset retinal dystrophy and early onset retinitis pigmentosa

Journal: La Tunisie medicale

Published: January 13, 2016

Epidemiologic study of hyperopia in schoolchildren in Tunisia

Epidemiologic study of hyperopia in schoolchildren in Tunisia

Journal: La Tunisie medicale

Published: April 17, 2015

Optical coherence tomography and fundus autofluorescence in Best macular dystrophy

Optical coherence tomography and fundus autofluorescence in Best macular dystrophy

Journal: Journal francais d'ophtalmologie

Published: February 19, 2015

Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients.

Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients.

Journal: PloS one

Published: October 06, 2014

Clinical characterization of the Stargardt disease and molecular exploration of the c.2041C>T mutation (ABCA4 gene) in Tunisian patients

Clinical characterization of the Stargardt disease and molecular exploration of the c.2041C>T mutation (ABCA4 gene) in Tunisian patients

Journal: Annales de biologie clinique

Published: December 18, 2013

SD-OCT contribution in congenital achromatopsia diagnosis (6 patients)

SD-OCT contribution in congenital achromatopsia diagnosis (6 patients)

Journal: Journal francais d'ophtalmologie

Published: June 22, 2013

Macular choroidal thickness assessment with SD-OCT in high myopia with or without choroidal neovascularization

Macular choroidal thickness assessment with SD-OCT in high myopia with or without choroidal neovascularization

Journal: Journal francais d'ophtalmologie

Published: November 21, 2012

Choroidal thickness measurement in highly myopic eyes using SD-OCT.

Choroidal thickness measurement in highly myopic eyes using SD-OCT.

Journal: Ophthalmic surgery, lasers & imaging : the official journal of the International Society for Imaging in the Eye

Published: September 07, 2012

Clinical polymorphism of stargardt disease in a large consanguineous tunisian family; implications for nosology.

Clinical polymorphism of stargardt disease in a large consanguineous tunisian family; implications for nosology.

Journal: Journal of ophthalmic & vision research

Published: July 24, 2012

A novel homozygous R764H mutation in crumbs homolog 1 causes autosomal recessive retinitis pigmentosa.

A novel homozygous R764H mutation in crumbs homolog 1 causes autosomal recessive retinitis pigmentosa.

Journal: Molecular vision

Published: April 26, 2012

Showing 1-11 of 11

Last Updated: 09/26/2026