Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients von Riahi, Zied, Bonnet, Crystel, Zainine, Rim, Lahbib, Saida, Bouyacoub, Yosra, Bechraoui, Rym, Marrakchi, Jihène, Hardelin, Jean-Pierre, Louha, Malek, Largueche, Leila, Ben Yahia, Salim, Kheirallah, Moncef, Elmatri, Leila, Besbes, Ghazi, Abdelhak, Sonia, Petit, Christine

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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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Clinical polymorphism of stargardt disease in a large consanguineous tunisian family; implications for nosology von El Matri, Leila, Ouechtati, Farah, Chebil, Ahmed, Largueche, Leila, Abdelhak, Sonia

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Choroidal Metastasis from Breast Cancer in a Male Patient Treated Successfully with Systemic Chemotherapy von Lagha, Aymen, Ayadi, Mouna, Largueche, Leila, Krimi, Sarra, Chraiet, Nesrine, Allani, Bassem, Rifi, Hela, Raies, Henda, Elmatri, Leila, Mezlini, Amel

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Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 gene von Said, Mariem Ben, Chouchène, Ebtissem, Salem, Salma Ben, Daoud, Kods, Largueche, Leila, Bouassida, Walid, Benzina, Zeineb, Ayadi, Hammadi, Söderkvist, Peter, Matri, Leila, Hmani-Aifa, Mounira

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A novel homozygous R764H mutation in crumbs homolog 1 causes autosomal recessive retinitis pigmentosa von Tiab, Leila, Largueche, Leila, Chouchane, Ibtissem, Derouiche, Kaouthar, Munier, Francis L, El Matri, Leila, Schorderet, Daniel F

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Epidemiologic study of myopia in a population of schoolchildren in Tunisia von Chebil, Ahmed, Jedidi, Lina, Chaker, Nibrass, Kort, Fedra, Largueche, Leila, El Matri, Leila

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Molecular exploration of the R91W (RPE65 gene) in Tunisian patients with early onset retinal dystrophy and early onset retinitis pigmentosa von Chouchene, Ibtissem, Largueche, Leila, Derouiche, Kaouther, Mabrouk, Souad, Abdelhak, Sonia, El Matri, Leila

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Epidemiologic study of hyperopia in schoolchildren in Tunisia von Chebil, Ahmed, Jeddidi, Lina, Chaker, Nibrass, Kort, Fedra, Bouladi, Mejda, Largueche, Leila, Limaiem, Rym, Mghaieth, Fatma, El Matri, Leila

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Clinical characterization of the Stargardt disease and molecular exploration of the c.2041C>T mutation (ABCA4 gene) in Tunisian patients von Chouchene, Ibtissem, Largueche, Leila, Ouechtati, Farah, Derouiche, Kawthar, Turki, Ahmed, Abdelhak, Sonia, El Matri, Leila

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Whole Exome Sequencing Identifies Mutations in Usher Syndrome Genes in Profoundly Deaf Tunisian Patients: e0120584 von Riahi, Zied, Bonnet, Crystel, Zainine, Rim, Lahbib, Saida, Bouyacoub, Yosra, Bechraoui, Rym, Marrakchi, Jihene, Hardelin, Jean-Pierre, Louha, Malek, Largueche, Leila

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Identification of a novel mutation in FOXL2 gene that leads to blepharophimosis ptosis epicanthus inversus and telecanthus syndrome in a Tunisian consanguineous family von Chouchene, Ibtissem, Derouiche, Kaouthar, Chaabouni, Afif, Cherif, Lamia, Amouri, Ahlem, Largueche, Leila, Abdelhak, Sonia, El Matri, Leila

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Optical Coherence Tomographic Findings in Berlin's Edema von El Matri, Leila, Chebil, Ahmed, Kort, Fedra, Bouraoui, Rym, Largueche, Leila, Mghaieth, Fatma

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Optical Coherence Tomography Findings in Berlin's Edema von El Matri, Leila, Chebil, Ahmed, Kort, Fedra, Bouraoui, Rym, Largueche, Leila, Mghaieth, Fatma

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Optical Coherence Tomographic Findings in Berlin′s Edema von Leila El Matri, Ahmed Chebil, Fedra Kort, Rym Bouraoui, Leila Largueche, Fatma Mghaieth

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Caractérisation clinique de la maladie de Stargardt et exploration moléculaire de la c.2041C>T (gène ABCA4) chez des patients tunisiens von CHOUCHENE, Ibtissem, LARGUECHE, Leila, OUECHTATI, Farah, DEROUICHE, Kawthar, TURKI, Ahmed, ABDELHAK, Sonia, EL MATRI, Leila

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Optical Coherence Tomographic Findings in Berlin's Edema von El Matri, Leila, Chebil, Ahmed, Kort, Fedra, Bouraoui, Rym, Largueche, Leila, Mghaieth, Fatma

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Identification of a novel mutation in FOXL2 gene that leads to blepharophimosis ptosis epicanthus inversus and telecanthus syndrome in a Tunisian consanguineous family von Chouchene, Ibtissem, Derouiche, Kaouthar, Chaabouni, Afif, Cherif, Lamia, Amouri, Ahlem, Largueche, Leila, Abdelhak, Sonia, El Matri, Leila

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Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients von Ouadani, Hanen, Ben-Mustapha, Imen, Ben-ali, Meriem, Ben-khemis, Leila, Larguèche, Beya, Boussoffara, Raoudha, Maalej, Sonia, Fetni, Ilhem, Hassayoun, Saida, Mahfoudh, Abdelmajid, Mellouli, Fethi, Yalaoui, Sadok, Masmoudi, Hatem, Bejaoui, Mohamed, Barbouche, Mohamed-Ridha

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Femmes du Maghreb von AMRANE, Djamila, Benadada, Assia, BENBRAHIM, Malha, Benmansour, Amina, BESSIS, Sophie, Boehringer, Sandra, DAKHLIA, Jocelyne, Dubesset, Mathilde, FERRON, Laurent, Fine, Agnès, GAILLARD, Cécile, GRANGAUD, Isabelle, HADDAD, Zoubida, KATZENELLENBOGEN, Simon, Khodja, Soumya Ammar, Knibiehler, Yvonne, Ladjimi Sebaï, Leïla, LAOUEDJ, Zineb, LARGUECHE, Dalenda, LEDUC, Agnès FINE et Claudine, LIAUZU, Claude, LUC, Jean-Noël, MARAND-FOUQUET, Catherine, Messaoudi, Leila, MORTIMER, Mildred, NETTER, Marie Laurence, SCHULZ, Kristina, SOIHET, Rachel, Sraieb, Noureddine, YACINE, Tassadit

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