Dental treatment approaches of amelogenesis imperfecta in children and young adults: A systematic review of the literature by Rhaiem, Miniar, Chalbi, Manel, Bousaid, Soumaya, Zouaoui, Wiem, Chemli, Mohamed Ali

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Epileptic encephalopathy and amelogenesis imperfecta: What about KohlschüttereTönz syndrome? Case report and literature review by chalbi, Manel, Nefzaoui, Meriem, Rhaiem, Miniar, boussaid, Soumaya, chemli, Mohamed ali

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Les enfants nord-africains atteints de fente labio-palatine unilatérale diffèrent-ils des individus normaux en termes de maturité dentaire ? Une étude pilote by Chalbi, Manel, Khemiss, Mehdi, Rhaiem, Miniar, Elabed, Nadia, Chemli, Mohamed Ali

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Inherited IL-12p40 Deficiency: Genetic, Immunologic, and Clinical Features of 49 Patients From 30 Kindreds by Prando, Carolina, Samarina, Arina, Bustamante, Jacinta, Boisson-Dupuis, Stéphanie, Cobat, Aurelie, Picard, Capucine, AlSum, Zobaida, Al-Jumaah, Suliman, Al-Hajjar, Sami, Frayha, Husn, Al-Mousa, Hamoud, Ben-Mustapha, Imen, Adimi, Parisa, Feinberg, Jacqueline, de Suremain, Maylis, Jannière, Lucile, Filipe-Santos, Orchidée, Mansouri, Nahal, Stephan, Jean-Louis, Nallusamy, Revathy, Kumararatne, Dinakantha S., Bloorsaz, Mohamad Reza, Ben-Ali, Meriem, Elloumi-Zghal, Houda, Chemli, Jalel, Bouguila, Jihene, Bejaoui, Mohamed, Alaki, Emadia, AlFawaz, Tariq S., Al Idrissi, Eman, ElGhazali, Gehad, Pollard, Andrew J., Murugasu, Belinda, Wah Lee, Bee, Halwani, Rabih, Al-Zahrani, Mohammed, Al Shehri, Mohammed A., Al-Zahrani, Mofareh, Bin-Hussain, Ibrahim, Mahdaviani, Seyed Alireza, Parvaneh, Nima, Abel, Laurent, Mansouri, Davood, Barbouche, Ridha, Al-Muhsen, Saleh, Casanova, Jean-Laurent

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Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988–2012) by Mellouli, Fethi, Mustapha, Imen Ben, Khaled, Monia Ben, Besbes, Habib, Ouederni, Monia, Mekki, Najla, Ali, Meriem Ben, Larguèche, Beya, Hachicha, Mongia, Sfar, Tahar, Gueddiche, Neji, Barsaoui, Siheme, Sammoud, Azza, Boussetta, Khadija, Becher, Saida Ben, Meherzi, Ahmed, Guandoura, Najoua, Boughammoura, Lamia, Harbi, Abdelaziz, Amri, Fethi, Bayoudh, Fethi, Jaballah, Najla Ben, Tebib, Neji, Bouaziz, Asma, Mahfoudh, Abdelmajid, Aloulou, Hajer, Mansour, Lamia Ben, Chabchoub, Imen, Boussoffara, Raoudha, Chemli, Jalel, Bouguila, Jihène, Hassayoun, Saida, Hammami, Saber, Habboul, Zakia, Hamzaoui, Agnès, Ammar, Jamel, Barbouche, Mohamed-Ridha, Bejaoui, Mohamed

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X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations by Aadam, Zahra, Kechout, Nadia, Barakat, Abdelhamid, Chan, Koon-Wing, Ben-Ali, Meriem, Ben-Mustapha, Imen, Zidi, Fethi, Ailal, Fatima, Attal, Nabila, Doudou, Fatouma, Abbadi, Mohamed-Cherif, Kaddache, Chawki, Smati, Leila, Touri, Nabila, Chemli, Jalel, Gargah, Tahar, Brini, Ines, Bakhchane, Amina, Charoute, Hicham, Jeddane, Leila, El Atiqi, Sara, El Hafidi, Naïma, Hida, Mustapha, Saile, Rachid, Alj, Hanane Salih, Boukari, Rachida, Bejaoui, Mohamed, Najib, Jilali, Barbouche, Mohamed-Ridha, Lau, Yu-Lung, Mellouli, Fethi, Bousfiha, Ahmed Aziz

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A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients by Ben-Farhat, Khaoula, Ben-Mustapha, Imen, Ben-Ali, Meriem, Rouault, Karen, Hamami, Saber, Mekki, Najla, Ben-chehida, Amel, Larguèche, Beya, Fitouri, Zohra, Abdelmoula, Selim, khemiri, Monia, Guediche, Mohamed-Neji, Boukthir, Samir, Barsaoui, Sihem, Chemli, Jalel, Barbouche, Mohamed-Ridha

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Clinical, Immunological and Genetic Findings of a Large Tunisian Series of Major Histocompatibility Complex Class II Deficiency Patients by Ben-Mustapha, Imen, Ben-Farhat, Khaoula, Guirat-Dhouib, Naouel, Dhemaied, Emna, Larguèche, Beya, Ben-Ali, Meriem, Chemli, Jalel, Bouguila, Jihène, Ben-Mansour, Lamia, Mellouli, Fethi, Khemiri, Monia, Béjaoui, Mohamed, Barbouche, Mohamed-Ridha

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A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients by Ben-Mustapha, Imen, Ben-Ali, Meriem, Mekki, Najla, Patin, Etienne, Harmant, Christine, Bouguila, Jihène, Elloumi-Zghal, Houda, Harbi, Abdelaziz, Béjaoui, Mohamed, Boughammoura, Lamia, Chemli, Jalel, Barbouche, Mohamed-Ridha

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Syndrome auriculo-temporal (Syndrome de Frey) : à propos d’une observation familiale by Chemli, M., Youssef, M., BelHadj Ali, H., Mohamed, M., Zili, J.

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