Genetic spectrum of retinal dystrophies in Tunisia von Habibi, Imen, Falfoul, Yosra, Turki, Ahmed, Hassairi, Asma, El Matri, Khaled, Chebil, Ahmed, Schorderet, Daniel F., El Matri, Leila

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Macular Dystrophy with Bilateral Macular Telangiectasia Related to the CYP2U1 Pathogenic Variant Assessed with Multimodal Imaging Including OCT-Angiography von El Matri, Khaled, Falfoul, Yousra, Habibi, Imen, Chebil, Ahmed, Schorderet, Daniel, El Matri, Leila

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Autosomal-Recessive Posterior Microphthalmos Is Caused by Mutations in PRSS56, a Gene Encoding a Trypsin-Like Serine Protease von Gal, Andreas, Rau, Isabella, El Matri, Leila, Kreienkamp, Hans-Jürgen, Fehr, Susanne, Baklouti, Karim, Chouchane, Ibtissem, Li, Yun, Rehbein, Monika, Fuchs, Josefine, Fledelius, Hans C., Vilhelmsen, Kaj, Schorderet, Daniel F., Munier, Francis L., Ostergaard, Elsebet, Thompson, Debra A., Rosenberg, Thomas

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Subthreshold micropulse laser adjuvant to bevacizumab versus bevacizumab monotherapy in treating diabetic macular edema: one- year- follow-up von El Matri, Leila, Chebil, Ahmed, El Matri, Khaled, Falfoul, Yousra, Chebbi, Zouheir

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Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB) von Habibi, Imen, Falfoul, Yosra, Todorova, Margarita G, Wyrsch, Stefan, Vaclavik, Veronika, Helfenstein, Maria, Turki, Ahmed, Matri, Khaled El, Matri, Leila El, Schorderet, Daniel F

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Management of a bilateral post-uveitic complex glaucoma with pupillary block, rupture of the anterior lens capsule, and malignant glaucoma following laser peripheral iridotomies: C... von El Matri, Khaled, Gouider, Dhouha, Limaiem, Rim, Chebil, Ahmed, Henchiri, Meher, Falfoul, Yousra, El Matri, Leila

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Multimodal imaging in retinitis pigmentosa: Correlations among microvascular changes, macular function and retinal structure von Falfoul, Yousra, Elleuch, Issam, El Matri, Khaled, Ghali, Hela, Hassairi, Asma, Chebil, Ahmed, Chaker, Nibrass, El Matri, Leila

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Sunrays epiretinal membrane von Hachicha, Ines, El Matri, Khaled, Rim, Bouraoui, Fatma, Mghaieth, Limaiem, Rim, El Matri, Leila

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The use of anterior segment optical coherence tomography in infectious keratitis von Hassairi, Asma, Jendoubi, Fahd, Fendouli, Ines, Limaiem, Rim, El Matri, Leila

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Central retinal artery occlusion after spinal surgery: Case report and literature review von Rmili, Mohamed Foued, Chebil, Ahmed, El Matri, Khaled, Werda, Slim, Falfoul, Yousra, Matri, Leila El

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Multimodal imaging of focal choroidal excavation and macular choroidal cavitation associated to choroidal neovascularization von El Matri, Khaled, Saidane, Rahma, Bouazzaoui, Ouafi, Hachicha, Iness, Falfoul, Yousra, Matri, Leila El

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Bilateral central retinal vein occlusion following COVID-19 vaccination: Cause or coincidence? von Matri, Khaled El, Werda, Slim, Chebbi, Zouheir, Saidane, Rahma, Doukh, Meryem, Choura, Racem, Falfoul, Yousra, Limaiem, Rim, Matri, Leila El

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Characteristics of Astigmatism in a Population of Tunisian School-Children von Chebil, Ahmed, Jedidi, Lina, Chaker, Nibrass, Kort, Fedra, Limaiem, Rym, Mghaieth, Fatma, El Matri, Leila

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Atypical presentation of bilateral iridoschisis with abnormal visibility of iris vessels: Role of anterior segment optical coherence tomography von Ben Aoun, Safa, Hachicha, Ines, Bouraoui, Rim, Matri, Khaled El, Limaiem, Rim, Matri, Leila El

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Granulomatous uveitis and reactive arthritis as manifestations of post-streptococcal syndrome von Abderrahim, Kais, Chebil, Ahmed, Falfoul, Yosra, Bouladi, Mejda, Matri, Leila El

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Optic disc and choroidal metastases secondary to breast cancer: A case report von Bouraoui, Rim, El Matri, Khaled, Falfoul, Yousra, Chelly, Zied, Chebil, Ahmed, Mghaieth, Fatma, Matri, Leila El

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Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New ABCA4 Mutations von El Matri, Leila, Hassairi, Asma, Chebil, Ahmed, Turki, Ahmed, Habibi, Imen, Falfoul, Yousra, Schorderet, Daniel F.

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Identifying mutations in Tunisian families with retinal dystrophy von Habibi, Imen, Chebil, Ahmed, Falfoul, Yosra, Allaman-Pillet, Nathalie, Kort, Fedra, Schorderet, Daniel F., El Matri, Leila

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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 von Ouechtati, Farah, Merdassi, Ahlem, Bouyacoub, Yosra, Largueche, Leila, Derouiche, Kaouther, Ouragini, Houyem, Nouira, Sonia, Tiab, Leila, Baklouti, Karim, Rebai, Ahmed, Schorderet, Daniel F, Munier, Francis L, Zografos, Leonidas, Abdelhak, Sonia, Matri, Leila El

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Swept Source Optical Coherence Tomography Angiography: Characteristic Findings in Type 3 Macular Neovascularization von Matri, Khaled El, Falfoul, Yousra, Chebil, Ahmed, Bouraoui, Rim, Hassairi, Asma, Matri, Leila El

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