Showing results (61-70 of 71) with videos related to
Sort By:
Pageof 8
Biomarker Research|August 29, 2014
Vascular endothelial growth factor genetic polymorphisms and susceptibility to age-related macular degeneration in Tunisian populationImen Habibi, Imen Sfar, Ahmed Chebil, et al.International Ophthalmology|May 3, 2020
Posterior staphylomas in non-highly myopic eyes with retinitis pigmentosaLeila El Matri, Yousra Falfoul, Khaled El Matri, et al.Journal of Current Ophthalmology|July 6, 2026
Two-Year Follow-Up of Idiopathic Acute Exudative Polymorphous Vitelliform Maculopathy: Case Report and Literature ReviewKhaled El Matri, Mohamed Foued Rmili, Ahmed Arfaoui, et al.Genes|November 27, 2019
Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)Imen Habibi, Yosra Falfoul, Margarita G Todorova, et al.Genes|May 8, 2020
Correction: Habibi I. et al. "Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)" Genes, 2019, 10, 953Imen Habibi, Yosra Falfoul, Margarita G Todorova, et al.La Tunisie Medicale|July 25, 2007
Does lowering hyperhomocysteinemia by folic acid beneficial for oculo-Behcet's disease? A pilot studyMohamed H Houman, Hajer Naffati, Monia Khanfir, et al.Ophthalmic Genetics|July 20, 2019
Granular type I corneal dystrophy in a large consanguineous Tunisian family with homozygous p.R124S mutation in the TGFBI geneYosra Bouyacoub, Yousra Falfoul, Mariem Ouederni, et al.Human Genetics|July 11, 2002
Allelic and locus heterogeneity in autosomal recessive gelatinous drop-like corneal dystrophyZhaoxia Ren, Pei-Yu Lin, Gordon K Klintworth, et al.Journal of Human Genetics|November 26, 2010
Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 geneFarah Ouechtati, Ahlem Merdassi, Yosra Bouyacoub, et al.American Journal of Human Genetics|March 15, 2011
Autosomal-recessive posterior microphthalmos is caused by mutations in PRSS56, a gene encoding a trypsin-like serine proteaseAndreas Gal, Isabella Rau, Leila El Matri, et al.Pageof 8