Genetic heterogeneity of megaloblastic anaemia type 1 in Tunisian patients von Bouchlaka, Chiraz, Maktouf, Chokri, Mahjoub, Bahri, Ayadi, Abdelkarim, Sfar, M. Tahar, Sioud, Mahbouba, Gueddich, Neji, Belhadjali, Zouheir, Rebaï, Ahmed, Abdelhak, Sonia, Dellagi, Koussay

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Polymorphism in transporter antigen peptides gene (TAP1) associated with atopy in Tunisians von Ismaïl, Awatef, Bousaffara, Raoudha, Kaziz a, Jannet, Zili, Jamel, el Kamel, Ali, Tahar Sfar, M., Remadi, Sami, Chouchane, Lotfi

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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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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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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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Pentosidine: Can be Related to the Etiology of Chronic Kidney Disease? von M, Kerkeni, H, Bouzidi, L, Ahmed, M, Hammami

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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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