Post-traumatic pseudoaneurysm of the superficial temporal artery: A rare cause of facial mass von Mizouni, Habiba, Hedhli, Mohamed, Zainine, Rym, Sahtout, Samia, Besbes, Ghazi, Menif, Emna

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Maxillary sinus arteriovenous malformation: A rare clinical entity von Marrakchi, Jihène, Chahed, Houda, Zainine, Rym, Mizouni, Habiba, Sahtout, Semia, Beltaief, Nejeh, Mnif, Emna, Besbes, Ghazi

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Otosclerosis Surgery: Contribution of Imaging in Surgical Failures and Labyrinthine Complications Diagnosis von Jrad, Myriam, Mabrouk, Asma Ben, Othmen, Aymen Ben, Marrakchi, Jihene, Zaidi, Anis, Zainine, Rym, Besbes, Ghazi, Mizouni, Habiba

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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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Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness von Riahi, Zied, Bonnet, Crystel, Zainine, Rim, Louha, Malek, Bouyacoub, Yosra, Laroussi, Nadia, Chargui, Mariem, Kefi, Rym, Jonard, Laurence, Dorboz, Imen, Hardelin, Jean-Pierre, Salah, Sihem Belhaj, Levilliers, Jacqueline, Weil, Dominique, McElreavey, Kenneth, Boespflug, Odile Tanguy, Besbes, Ghazi, Abdelhak, Sonia, Petit, Christine

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Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss von Riahi, Zied, Hammami, Hassen, Ouragini, Houyem, Messai, Habib, Zainine, Rim, Bouyacoub, Yosra, Romdhane, Lilia, Essaid, Donia, Kefi, Rym, Rhimi, Mohsen, Bedoui, Monia, Dhaouadi, Afef, Feldmann, Delphine, Jonard, Laurence, Besbes, Ghazi, Abdelhak, Sonia

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Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome von Riahi, Zied, Zainine, Rim, Mellouli, Yosra, Hannachi, Raja, Bouyacoub, Yosra, Laroussi, Nadia, Beltaief, Najeh, Kefi, Rym, Romdhane, Lilia, Bonnet, Crystel, Abdelhak, Sonia, Besbes, Ghazi

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A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families von Riahi, Zied, Chahed, Houda, Jaafoura, Habib, Zainine, Rim, Messaoud, Olfa, Naili, Mohamed, Nagara, Majdi, Hammami, Hassan, Laroussi, Nadia, Bouyacoub, Yosra, Kefi, Rym, Bonnet, Crystel, Besbes, Ghazi, Abdelhak, Sonia

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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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