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Immunoelectrophoretic and T cell study in neurobehcet disease von Kchaou, M., Belghuith, M., Bahrini, K., Echebbi, S., Jamoussi, H., Fray, S., Ben Ali, N., Fredj, M.

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Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome von Kallabi, Fakhri, Belghuith, Neila, Aloulou, Hajer, Kammoun, Thouraya, Ghorbel, Soufiane, Hajji, Mouna, Gallas, Syrine, Chemli, Jaleleddine, Chabchoub, Imen, Azzouz, Hatem, Ben Chehida, Amel, Sfaihi, Lamia, Makni, Saloua, Amouri, Ali, Keskes, Leila, Tebib, Neji, Ben Becher, Saayda, Hachicha, Monjia, Kamoun, Hassen

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Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria von Jellouli, Nadege Kammoun, Hadj Salem, Ikhlass, Ellouz, Emna, Kamoun, Zeineb, kamoun, Fatma, tlili, Abdelaziz, Kaabachi, Naziha, Triki, Chanez, Fakhfakh, Faiza

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Molecular confirmation of founder mutation c.-167A>G in Tunisian patients with PMLD disease von Kammoun Jellouli, Nadege, Hadj Salem, Ikhlass, Ellouz, Emna, Louhichi, Nacim, tlili, Abdelaziz, Kammoun, Fatma, Triki, Chanez, Fakhfakh, Faiza

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