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收藏Sideroblastic anemia in children: challenges in diagnosis and management in three cases
Rekaya, Samia; Ben Fraj, Ilhem; Hamdi, Rym; Ben Taieb, Aicha; Merdassi, Amani; Jouini, Hamida; Zarrouk, Hajer; Zaiter, Ikram; Kouki, Ridha; Bejaoui, Mohamed; Mellouli, Fethi; Ben Khaled, Monia; Ouederni, Monia 分享 收藏 分享 收藏 Diagnostic challenge in a series of eleven patients with hyper IgE syndromesYaakoubi, Roukaya; Mekki, Najla; Ben-Mustapha, Imen; Ben-Khemis, Leila; Bouaziz, Asma; Ben Fraj, Ilhem; Ammar, Jamel; Hamzaoui, Agnes; Turki, Hamida; Boussofara, Lobna; Denguezli, Mohamed; Haddad, Samir; Ouederni, Monia; Bejaoui, Mohamed; Chan, Koon Wing; Lau, Yu Lung; Mellouli, Fethi; Barbouche, Mohamed-Ridha; Ben-Ali, Meriem 分享 收藏 Containment of Local COVID-19 Outbreak Among Hematopoietic Stem Cell Transplant Recipients and Healthcare Workers in a Pediatric Stem Cell UnitOuederni, Monia; Rekaya, Samia; Bouabdallah, Oussema; Ben Fradj, Ilhem; Kouki, Ridha; Chebbi, Yosr; Ammar, Sahar Ben; Lamouchi, Takwa; Lachiheb, Asma; Zekri, Nessrine; Laajili, Siwar; Zaiter, Ikram; Hamzaoui, Agnes; Bejaoui, Mohamed; Mellouli, Fethi; Achour, Wafa; Ben Khaled, Monia 分享 收藏 Effect of oleuropein on oxidative stress, inflammation and apoptosis induced by ischemia-reperfusion injury in rat kidneyNasrallah, Hana; Aissa, Imen; Slim, Cherifa; Boujbiha, Mohamed Ali; Zaouali, Mohamed Amine; Bejaoui, Mohamed; Wilke, Victoria; Jannet, Hichem Ben; Mosbah, Habib; Abdennebi, Hassen Ben 分享 收藏 A Phase 3 Trial of Luspatercept in Patients with Transfusion-Dependent β-ThalassemiaLuspatercept在输血依赖性 β-地中海贫血患者中的3期试验Cappellini, M. D.; Viprakasit, V.; Taher, A. T.; Georgiev, P.; Kuo, K. H. M.; Coates, T.; Voskaridou, E.; Liew, H. -K.; Pazgal-Kobrowski, I.; Forni, G. L.; Perrotta, S.; Khelif, A.; Lal, A.; Kattamis, A.; Vlachaki, E.; Origa, R.; Aydinok, Y.; Bejaoui, M.; Ho, P. J.; Chew, L. -P.; Bee, P. -C.; Lim, S. -M.; Lu, M. -Y.; Tantiworawit, A.; Ganeva, P.; Gercheva, L.; Shah, F.; Neufeld, E. J.; Thompson, A.; Laadem, A.; Shetty, J. K.; Zou, J.; Zhang, J.; Miteva, D.; Zinger, T.; Linde, P. G.; Sherman, M. L.; Hermine, O.; Porter, J.; Piga, A. 分享 收藏 Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous FamiliesBen-Ali, Meriem; Kechout, Nadia; Mekki, Najla; Yang, Jing; Chan, Koon Wing; Barakat, Abdelhamid; Aadam, Zahra; Gamara, Jouda; Gargouri, Lamia; Largueche, Beya; BelHadj-Hmida, Nabil; Nedri, Amel; Ben Ameur, Houcine; Mellouli, Fethi; Boukari, Rachida; Bejaoui, Mohamed; Bousfiha, Aziz; Ben-Mustapha, Imen; Lau, Yu-Lung; Barbouche, Mohamed-Ridha 分享 收藏 Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseasesMensa-Vilaro, Anna; Bravo Garcia-Morato, Maria; de la Calle-Martin, Oscar; Franco-Jarava, Clara; Teresa Martinez-Saavedra, Maria; Gonzalez-Granado, Luis I.; Gonzalez-Roca, Eva; Luis Fuster, Jose; Alsina, Laia; Mutchinick, Osvaldo M.; Balderrama-Rodriguez, Angelica; Ramos, Eduardo; Modesto, Consuelo; Mesa-del-Castillo, Pablo; Ortego-Centeno, Norberto; Clemente, Daniel; Souto, Alejandro; Palmou, Natalia; Remesal, Agustin; Leslie, Kieron S.; Gomez de la Fuente, Enrique; Bravo Gallego, Luz Yadira; Maria Campistol, Josep; Guirat Dhouib, Naouel; Bejaoui, Mohamed; Almeida Dutra, Livia; Teresa Terreri, Maria; Mosquera, Catalina; Gonzalez, Tatiana; Canellas, Jeronima; Maria Garcia-Ruiz de Morales, Jose; Wouters, Carine H.; Teresa Bosque, Maria; Cham, Weng Tarng; Jimenez-Trevino, Santiago; de Inocencio, Jaime; Bloomfield, Marketa; Perez de Diego, Rebeca; Martinez-Pomar, Natalia; Rodriguez-Pena, Rebeca; Gonzalez-Santesteban, Cecilia; Soler-Palacin, Pere; Casals, Ferran; Yague, Jordi; Allende, Luis M.; Carlos Rodriguez-Gallego, Jose; Colobran, Roger; Martinez-Martinez, Laura; Lopez-Granados, Eduardo; Arostegui, Juan I. 分享 收藏 The effect of zinc acexamate on oxidative stress, inflammation and mitochondria induced apoptosis in rat model of renal warm ischemiaAbdallah, Najet Hadj; Baulies, Anna; Bouhlel, Ahlem; Bejaoui, Mohamed; Zaouali, Mohamed Amine; Ben Mimouna, Safa; Messaoudi, Imed; Carlos Fernandez-Checa, Jose; Garcia Ruiz, Carmen; Ben Abdennebi, Hassen 分享 收藏 分享 收藏 分享 收藏 A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patientsBen-Khemis, Leila; Mekki, Najla; Ben-Mustapha, Imen; Rouault, Karen; Mellouli, Fethi; Khemiri, Monia; Bejaoui, Mohamed; Essaddam, Leila; Ben-Becher, Saayda; Boughamoura, Lamia; Hassayoun, Saida; Ben-Ali, Meriem; Barbouche, Mohamed-Ridha 分享 收藏 Homozygous transcription factor 3 gene (TCF3) mutation is associated with severe hypogammaglobulinemia and B-cell acute lympho blastic leukemiaBen-Ali, Meriem; Yang, Jing; Chan, Koon Wing; Ben-Mustapha, Imen; Mekki, Najla; Benabdesselem, Chaouki; Mellouli, Fethi; Bejaoui, Mohamed; Yang, Wanling; Aissaoui, Lamia; Lau, Yu Lung; Barbouche, Mohamed-Ridha 分享 收藏 Myocardial and liver iron overload, assessed using T2*magnetic resonance imaging with an excel spreadsheet for post processing in Tunisian thalassemia major patientsOuederni, Monia; Ben Khaled, Monia; Mellouli, Fethi; Ben Fraj, Elhem; Dhouib, Nawel; Ben Yakoub, Ismehen; Abbes, Selem; Mnif, Nejla; Bejaoui, Mohamed 分享 收藏 分享 收藏 X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK MutationsAadam, 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, Naima; Hida, Mustapha; Saile, Rachid; Alj, Hanane Salih; Boukari, Rachida; Bejaoui, Mohamed; Najib, Jilali; Barbouche, Mohamed-Ridha; Lau, Yu-Lung; Mellouli, Fethi; Bousfiha, Ahmed Aziz 分享 收藏 分享 收藏 Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988-2012)Mellouli, Fethi; Ben Mustapha, Imen; Ben Khaled, Monia; Besbes, Habib; Ouederni, Monia; Mekki, Najla; Ben Ali, Meriem; Largueche, Beya; Hachicha, Mongia; Sfar, Tahar; Gueddiche, Neji; Barsaoui, Siheme; Sammoud, Azza; Boussetta, Khadija; Ben Becher, Saida; Meherzi, Ahmed; Guandoura, Najoua; Boughammoura, Lamia; Harbi, Abdelaziz; Amri, Fethi; Bayoudh, Fethi; Ben Jaballah, Najla; Tebib, Neji; Bouaziz, Asma; Mahfoudh, Abdelmajid; Aloulou, Hajer; Ben Mansour, Lamia; Chabchoub, Imen; Boussoffara, Raoudha; Chemli, Jalel; Bouguila, Jihene; Hassayoun, Saida; Hammami, Saber; Habboul, Zakia; Hamzaoui, Agnes; Ammar, Jamel; Barbouche, Mohamed-Ridha; Bejaoui, Mohamed 分享 收藏 The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency64例胞质分裂8缺乏症患者的扩展临床表型Engelhardt, Karin R.; Gertz, Michael E.; Keles, Sevgi; Schaeffer, Alejandro A.; Sigmund, Elena C.; Glocker, Cristina; Saghafi, Shiva; Pourpak, Zahra; Ceja, Ruben; Sassi, Atfa; Graham, Laura E.; Massaad, Michel J.; Mellouli, Fethi; Ben-Mustapha, Imen; Khemiri, Monia; Kilic, Sara Sebnem; Etzioni, Amos; Freeman, Alexandra F.; Thiel, Jens; Schulze, Ilka; Al-Herz, Waleed; Metin, Ayse; Sanal, Oezden; Tezcan, Ilhan; Yeganeh, Mehdi; Niehues, Tim; Dueckers, Gregor; Weinspach, Sebastian; Patiroglu, Turkan; Unal, Ekrem; Dasouki, Majed; Yilmaz, Mustafa; Genel, Ferah; Aytekin, Caner; Kutukculer, Necil; Somer, Ayper; Kilic, Mehmet; Reisli, Ismail; Camcioglu, Yildiz; Gennery, Andrew R.; Cant, Andrew J.; Jones, Alison; Gaspar, Bobby H.; Arkwright, Peter D.; Pietrogrande, Maria C.; Baz, Zeina; Al-Tamemi, Salem; Lougaris, Vassilios; Lefranc, Gerard; Megarbane, Andre; Boutros, Jeannette; Galal, Nermeen; Bejaoui, Mohamed; Barbouche, Mohamed-Ridha; Geha, Raif S.; Chatila, Talal A.; Grimbacher, Bodo 分享 收藏 
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