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The British Journal of Ophthalmology|April 21, 2021
Autosomal recessive congenital hereditary corneal dystrophy associated with a novel SLC4A11 mutation in two consanguineous Tunisian familiesZohra Chibani, Imen Zone Abid, Peter Söderkvist, et al.Clinical & Experimental Ophthalmology|June 30, 2019
Novel BEST1 gene mutations associated with two different forms of macular dystrophy in Tunisian familiesZohra Chibani, Imen Zone Abid, Annette Molbaek, et al.La Tunisie Medicale|September 20, 2019
Presumed Tuberculous uveitis: clinical features and managementSalma Gargouri, Imene Kaibi, Imen Zone, et al.Molecular Biology Reports|June 10, 2026
The co-occurrence of homozygous variants in GUCY2D and MYO7A in Leber congenital amaurosis associated with deafness: clinical, molecular, and in silico investigationMarwa Maalej, Lamia Sfaihi, Imen Zone Abid, et al.Journal of Ophthalmic Inflammation and Infection|November 30, 2016
Ocular involvement associated with varicella in adultsSalma Gargouri, Sana Khochtali, Sourour Zina, et al.Pageof 1