Value of troponin levels in the diagnosis of cardiac dysfunction in moderate scorpion envenomation von Chakroun-Walha, O, Karray, R, Jerbi, M, Ben Rebeh, A, Jammeli, C, Bahloul, M, Ammar, R, Chabchoub, I, Bouaziz, M, Nasri, A, Rekik, N

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Prevalence of comorbid asthma in Tunisian patients with COVID-19: clinical features and outcomes von Ben Rebeh, Imen, Gargouri, Marwa, Ghariani, Marwa, Kallel, Nesrine, Rouis, Sana, Marrakchi, Wafa, Chebil, Dhekra, Ben Marzoug, Riadh, Gargouri, Hela, Merzougui, Latifa, Ghorbel, Houda, Chakroun, Mohamed, Hadj Kacem, Hassen, Rebai, Ahmed

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Infected Primary Bone Mantle Cell Lymphoma with Multiple Vertebral Involvement von Bougossa, Rebeh, Larbi, Fatma, Mabrouk, Asma Ben, Jomaa, Olfa, Chelli, Jihene

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Tuberculose disséminée révélée par une localisation épididymaire chez un patient immunocompétent: à propos d’un cas von Bougossa, Rebeh, Ammari, Fatma Larbi, Mabrouk, Asma Ben, Jouirou, Rabeb, Arfa, Sondess, Chelli, Jihene

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Primary Spontaneous Pneumomediastinum and Extensive Cervical Emphysema in COVID-19 Infection: a Case Report von Marrakchi, Wafa, Ben Brahim, Hajer, Bougossa, Rebeh, Toumi, Adnene, Chakroun, Mohamed

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Disseminated tuberculosis revealed by epididymal localization in an immunocompetent patient: a case report von Bougossa, Rebeh, Ammari, Fatma Larbi, Mabrouk, Asma Ben, Jouirou, Rabeb, Arfa, Sondess, Chelli, Jihene

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Two missense mutations in SLC26A4 gene: a molecular and functional study von Rebeh, I Ben, Yoshimi, N, Hadj-Kacem, H, Yanohco, S, Hammami, B, Mnif, M, Araki, M, Ghorbel, A, Ayadi, H, Masmoudi, S, Miyazaki, H

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Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis von Ben-Rebeh, Imen, Grati, Mhamed, Bonnet, Crystel, Bouassida, Walid, Hadjamor, Imen, Ayadi, Hammadi, Ghorbel, Abdelmonem, Petit, Christine, Masmoudi, Saber

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Molecular Analysis of Libyan Families with Allgrove Syndrome: Geographic Expansion of the Ancestral Mutation c.1331+1G>A in North Africa von Kallabi, Fakhri, Ben Rebeh, Imen, Felhi, Rahma, Sellami, Dorra, Masmoudi, Saber, Keskes, Leila, Kamoun, Hassen

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Mutation in gap and tight junctions in patients with non-syndromic hearing loss von Belguith, Hanen, Tlili, Abedelaziz, Dhouib, Houria, Rebeh, Imen Ben, Lahmar, Imed, Charfeddine, Ilhem, Driss, Nabil, Ghorbel, Abdelmonem, Ayadi, Hammadi, Masmoudi, Saber

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Endoplasmic reticulum quality control is involved in the mechanism of endoglin-mediated hereditary haemorrhagic telangiectasia von Ali, Bassam R, Ben-Rebeh, Imen, John, Anne, Akawi, Nadia A, Milhem, Reham M, Al-Shehhi, Nouf A, Al-Ameri, Mouza M, Al-Shamisi, Shamma A, Al-Gazali, Lihadh

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A novel dominant mutation in SIX1 , affecting a highly conserved residue, result in only auditory defects in humans von Mosrati, Mohamed Ali, Hammami, Boutheina, Rebeh, Imen Ben, Ayadi, Leila, Dhouib, Leila, Ben mahfoudh, Khaireddine, Hakim, Bochra, Charfeddine, Ilhem, Mnif, Jameleddine, Ghorbel, Abdelmonem, Masmoudi, Saber

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TMC1 but Not TMC2 Is Responsible for Autosomal Recessive Nonsyndromic Hearing Impairment in Tunisian Families von Tlili, Abdelaziz, Rebeh, Imen Ben, Aifa-Hmani, Mounira, Dhouib, Houria, Moalla, Jihen, Tlili-Chouchène, Jihen, Said, Mariem Ben, Lahmar, Imed, Benzina, Zeineb, Charfedine, Ilhem, Driss, Nabil, Ghorbel, Abdelmonem, Ayadi, Hammadi, Masmoudi, Saber

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Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness von Ben Rebeh, Imen, Morinière, Madeleine, Ayadi, Leila, Benzina, Zeineb, Charfedine, Ilhem, Feki, Jamel, Ayadi, Hammadi, Ghorbel, Abdelmonem, Baklouti, Faouzi, Masmoudi, Saber

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Update on the Epidemiology of Scorpion Envenomation in the South of Tunisia von Chakroun-Walha, Olfa, Karray, Rim, Jerbi, Mouna, Nasri, Abdennour, Issaoui, Fadhila, Amine, Ben Rebeh, Bahloul, Mabrouk, Bouaziz, Mounir, Ksibi, Hichem, Rekik, Noureddine

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Perinatal lethal type II osteogenesis imperfecta: a case report von Ayadi, Imene Dahmane, Hamida, Emira Ben, Rebeh, Rania Ben, Chaouachi, Sihem, Marrakchi, Zahra

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Tuberculose disséminée révélée par une localisation épididymaire chez un patient immunocompétent: à propos d’un cas von Bougossa, Rebeh, Ammari, Fatma Larbi, Mabrouk, Asma Ben, Jouirou, Rabeb, Arfa, Sondess, Chelli, Jihene

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Localization of a Novel Autosomal Recessive Non‐syndromic Hearing Impairment Locus DFNB63 to Chromosome 11q13.3‐q13.4 von Tlili, A., Masmoudi, S., Dhouib, H., Bouaziz, S., Rebeh, I. Ben, Chouchen, J., Turki, K., Benzina, Z., Charfedine, I., Drira, M., Ayadi, H.

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Clinical and molecular analysis of isovaleric acidemia patients in the United Arab Emirates reveals remarkable phenotypes and four novel mutations in the IVD gene von Hertecant, Jozef L, Ben-Rebeh, Imen, Marah, Muhaned A, Abbas, Thikra, Ayadi, Leila, Ben Salem, Salma, Al-Jasmi, Fatma A, Al-Gazali, Lihadh, Al-Yahyaee, Said A, Ali, Bassam R

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Evolution of hypertension and diabetes in elderly subjects von Charrada, Ines, Tahri, Soumeya, Boubaker, Fadia, Arfa, Sondess, Bougossa, Rebeh, Brahim, Marwa Ben, Zantour, Beha, Alaya, Wafa, Berriche, Olfa, Sfar, Mohamed Habib

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