Long-Term Outcome of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency von Mnif, Mouna Feki, PhD, Kamoun, Mahdi, MD, Mnif, Fatma, MD, Charfi, Nadia, PhD, Kallel, Nozha, MD, Ben Naceur, Basma, MD, Rekik, Nabila, PhD, Abid, Mohamed, PhD, Mnif, Zainab, PhD, Sfar, Mohamed Habib, PhD, Sfar, Mohamed Tahar, PhD, Hachicha, Mongia, PhD, Keskes, Leila Ammar, PhD

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A cost-effectiveness analysis of PHiD-CV compared to PCV13 in a national immunization program setting in Tunisia von Lagoubi, Youness, Sfar, Mohamed Tahar, Gomez, Jorge A.

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Antioxidant enzymes activities in obese Tunisian children von Sfar, Sonia, Boussoffara, Raoudha, Sfar, Mohamed Tahar, Kerkeni, Abdelhamid

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Maternally Inherited Leigh Syndrome: T8993G Mutation in a Tunisian Family von Mkaouar-Rebai, Emna, PhD, Chaari, Wissem, MD, Younes, Samia, MD, Bousoffara, Raoudha, MD, Sfar, Mohamed Tahar, MD, Fakhfakh, Faiza, PhD

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Interrelationships between cadmium, zinc and antioxidants in the liver of the rat exposed orally to relatively high doses of cadmium and zinc von Jihen, El Heni, Sonia, Sfar, Fatima, Hammouda, Mohamed Tahar, Sfar, Abdelhamid, Kerkeni

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Congenital Adrenal Hyperplasia and Brain Magnetic Resonance Imaging Abnormalities von Samia, Younes-Mhenni, Mahdi, Kamoun, Baha, Zantour, Saida, Jerbi-Ommezine, Tahar, Sfar Mohamed, Habib, Sfar Mohamed

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West syndrome and mosaic trisomy 13: A case report von Ben Hamouda, Hechmi, Soua, Habib, Dogui, Mohamed, Hamza, Hassine, Sfar, Mohamed Tahar

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Localization of tissue transglutaminase and N (epsilon)-(gamma) -glutamyl lysine in duodenal cucosa during the development of mucosal atrophy in coeliac disease von SAKLY, Wahiba, SRIHA, Badreddine, GHEDIRA, Ibtissem, BIENVENU, Francoise, AYADI, Abdelkarim, MOHAMED TAHAR SFAR, LACHAUX, Alain, KORBI, Sadok, BIENVENU, Jacques, FABIEN, Nicole

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Fertility outcome in male and female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency von Kamoun, Mahdi, Mnif, Mouna Feki, Charfi, Nadia, Ben Naceur, Basma, Mnif, Fatma, Rekik, Nabila, Mnif, Zainab, Sfar, Mohamed Habib, Sfar, Mohamed Tahar, Hachicha, Mongia, Ben Salem, Azza, Keskes, Leila Ammar, Abid, Mohamed

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High frequency of W1327X mutation in glycogen storage disease type III patients from central Tunisia von CHERIF, Wafa, RHOUMA, Faten Ben, KAABACHI, Naziha, TAHAR SFAR, Mohamed, DRIDI, Marie-Françoise Ben, TEBIB, Neji, ABDELHAK, Sonia, MESSAI, Habib, MILI, Amira, GRIBAA, Moez, KEFI, Rym, AYADI, Abdelkarim, BOUGHAMOURA, Lamia, CHEMLI, Jelel, SAAD, Ali

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Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency von Mnif, Mouna Feki, Kamoun, Mahdi, Mnif, Fatma, Charfi, Nadia, Naceur, Basma Ben, Kallel, Nozha, Rekik, Nabila, Mnif, Zainab, Sfar, Mohamed Habib, Sfar, Mohamed Tahar, Hachicha, Mongia, Abid, Mohamed

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Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgene... von Mnif, Mouna, Kamoun, Mahdi, Mnif, Fatma, Charfi, Nadia, Kallel, Nozha, Rekik, Nabila, Naceur, Basma, Fourati, Hela, Daoud, Emna, Mnif, Zainab, Sfar, Mohamed, Younes-Mhenni, Samia, Sfar, Mohamed, Hachicha, Mongia, Abid, Mohamed

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Enterovirus meningitis in Tunisia (Monastir, Mahdia, 2011–2013): identification of virus variants cocirculating in France von Othman, Ines, Volle, Romain, Elargoubi, Aida, Guediche, Mohamed Neji, Chakroun, Mohamed, Sfar, Mohamed Tahar, Pereira, Bruno, Peigue-Lafeuille, Hélène, Aouni, Mahjoub, Archimbaud, Christine, Bailly, Jean-Luc

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Trace element status and fatty acids metabolism during healthy ageing: An example of a population from the Tunisian eastern coast von Sfar, Sonia, El Heni, Jihen, Laporte, François, Braham, Hamadi, Jawed, Abdelhafidh, Amor, Salah, Sfar, Mohamed Tahar, Kerkeni, Abdelhamid

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Genetic diseases in the Tunisian population von Romdhane, Lilia, Abdelhak, Sonia

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Primary resistance to clarithromycin, metronidazole and amoxicillin of Helicobacter pylori isolated from Tunisian patients with peptic ulcers and gastritis: a prospective multicent... von Ben Mansour, Khansa, Burucoa, Christophe, Zribi, Meriem, Masmoudi, Afef, Karoui, Sami, Kallel, Lamia, Chouaib, Soufiène, Matri, Samira, Fekih, Monia, Zarrouk, Sonia, Labbene, Mounir, Boubaker, Jalel, Cheikh, Imed, Hriz, Mongi Ben, Siala, Nadia, Ayadi, Abdelkarim, Filali, Azza, Mami, Nabil Ben, Najjar, Taoufik, Maherzi, Ahmed, Sfar, Mohamed Tahar, Fendri, Chedlia

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Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: Characterization of three novel polymorphisms von Ben Charfeddine, Ilhem, Riepe, Felix G., Clauser, Eric, Ayedi, Abdelkarim, Makni, Saloua, Sfar, Mohamed Tahar, Sboui, Hassen, Kahloul, Najoua, Ben Hamouda, Hechmi, Chouchane, Slaheddine, Trimech, Sihem, Zouari, Noura, M'Rabet, Samir, Amri, Fathi, Saad, Ali, Holterhus, Paul-Martin, Gribaa, Moez

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Neonatal duodenal obstruction due to a preduodenal portal vein associated with intestinal malrotation: A case report von Ben Hamouda, Hechmi, Hadj Salem, Radhia, Rabeh, Hatem, Ben Amor, Ilhem, Belhassen, Samia, Soua, Hahib, Nouri, Abdellatif, Ben Rhouma, Khaled, Hamza, Hassine, Mahjoub, Bahri, Sfar, Mohamed Tahar

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Contribution of laparoscopy in the abdominal tuberculosis diagnosis: retrospective study of about 11 cases von Chahed, Jamila, Mekki, Mongi, Mansour, Asma, Ben Brahim, Mohamed, Maazoun, Kais, Hidouri, Saida, Krichene, Imed, Sahnoun, Lassâad, Jouini, Riyadh, Belgith, Mohsen, Zakhama, Abdelfattah, Sfar, Mohamed Tahar, Gueddiche, Mohamed Neji, Harbi, Abdelaziz, Amri, Fethi, Mahfoudh, Abdelmajid, Nouri, Abdellatif

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L’atteinte neurologique au cours du Triple A syndrome : étude clinique et génétique d’une famille tunisienne von Mokni, Narjes, Younes, Samia, Ayadi, Abdelkrim, Sfar, Mohamed Tahar, Sfar, Mohamed Habib

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