Dental treatment approaches of amelogenesis imperfecta in children and young adults: A systematic review of the literature von 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 von chalbi, Manel, Nefzaoui, Meriem, Rhaiem, Miniar, boussaid, Soumaya, chemli, Mohamed ali

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Orofacial Manifestations in Apert Syndrome: A Case Report and a Review of the Literature von Nefzaoui, Mariem, Jazi, Imene, Zaroui, Jihene, Ali Chemli, Mohamed

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

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Cutaneous Alternariosis in a Renal Transplant Recipient von ESSABBAH, Nawel, GORSANE, Imen, ZILI, Jameleddine, ZAKHAMA, Abdelfatteh, SKHIRI, Habib, YOUSSEF, Monia, HADHRI, Rym, ALOUI, Sabra, GORCII, Mohamed, HICHEM BEL HADJ ALI, CHEMLI, Zeineb, BABBA, Hammouda, MEZRI EL MAY

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