| Issue Date | Title | Author(s) |
| 2010 | The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: Evidence for a founder effect in the Moroccan population | Naamane, Hamid; El Maataoui, Ouafaa; Ailal, Fatima; Barakat, Abdelhamid; Bennani, Siham; Najib, Jilali; Hassar, Mohammed; Saile, Rachid; Bousfiha, Ahmed Aziz |
| 2014 | Chronic granulomatous disease in Morocco: Genetic immunological and clinical features of 12 patients from 10 kindreds | Ait Baba, Laila; Ailal, Fatima; El Hafidi, Naima; Hubeau, Marjorie; Jabot-Hanin, Fabienne; Benajiba, Noufissa; Aadam, Zahra; Conti, Francesca; Deswarte, Caroline; Jeddane, Leila; Aglaguel, Ayoub; El Maataoui, Ouafaa; Tissent, Ahmed; Mahraoui, Chafiq; Najib, Jilali; Martinez-Barricarte, Ruben; Abel, Laurent; Habti, Norddine; Saile, Rachid; Casanova, Jean-Laurent; Bustamante, Jacinta; Salih Alj, Hanane; Bousfiha, Ahmed Aziz |
| 2016 | Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases | Conti, Francesca; Lugo-Reyes, Saul Oswaldo; Galicia, Lizbeth Blancas; He, Jianxin; Aksu, Guzide; de Oliveira, Edgar Borges; Deswarte, Caroline; Hubeau, Marjorie; Karaca, Neslihan; Suremain, Maylis de; Guerin, Antoine; Ait Baba, Laila; Prando, Carolina; G. Guerrero, Gloria; Emiroglu, Melike; Nur Oz, Fatma; Yamazaki Nakashimada, Marco Antonio; Serrano, Edith Gonzalez; Espinosa, Sara; Barlan, Isil; Perez, Nestor; Regairaz, Lorena; Guidos Morales, Hector Eduardo; Bezrodnik, Liliana; Di Giovanni, Daniela; Dbaibo, Ghassan; Ailal, Fatima; Galicchio, Miguel; Oleastro, Matias; Chemli, Jalel; Danielian, Silvia; Perez, Laura; Ortega, Maria Claudia; Lavin, Susana Soto; Hertecant, Joseph; Anal, Ozden; Kechout, Nadia; Al-Idrissi, Eman; ElGhazali, Gehad; Bondarenko, Anastasia; Chernyshova, Liudmyla; Ciznar, Peter; Herbigneaux, Rose-Marie; Diabate, Aminata; Ndaga, Stephanie; Konte, Barik; Czarna, Ambre; Migaud, Melanie; Pedraza-Sanchez, Sigifredo; Bano Zaidi, Mussaret; Vogt, Guillaume; Blanche, Stephane; Benmustapha, Imen; Mansouri, Davood; Abel, Laurent; Boisson-Dupuis, Stephanie; Mahlaoui, Nizar; Bousfiha, Ahmed Aziz; Picard, Capucine; Barbouche, Ridha; Al-Muhsen, Saleh; J. Espinosa-Rosales, Francisco; Condino-Neto, Antonio; Casanova, Jean-Laurent; Bustamante, Jacinta |
| 2013 | A phenotypic approach for IUIS PID classification and diagnosis: Guidelines for clinicians at the bedside | Bousfiha, Ahmed Aziz; Jeddane, Leïla; Ailal, Fatima; Al Herz, Waleed; Conley, Mary Ellen; Cunningham-Rundles, Charlotte; Etzioni, Amos; Fischer, Alain; Franco, Jose Luis; S. Geha, Raif; Hammarström, Lennart; Nonoyama, Shigeaki; D. Ochs, Hans; M. Roifman, Chaim; Seger, Reinhard; Tang, Mimi L. K.; M. Puck, Jennifer; Chapel, Helen; D. Notarangelo, Luigi; Casanova, Jean-Laurent |
| 2017 | Poikiloderma with Neutropenia in Morocco: a Report of Four Cases | Aglaguel, Ayoub; Abdelghaffar, Houria; Ailal, Fatima; Habti, Norddine; Hesse, Sebastian; Kohistani, Naschla; Klein, Christoph; Bousfiha, Ahmed Aziz |
| 2013 | Primary Immunodeficiency Diseases Worldwide: More Common than Generally Thought | Bousfiha, Ahmed Aziz; Jeddane, Leïla; Ailal, Fatima; Benhsaien, Ibtihal; Mahlaoui, Nizar; Casanova, Jean-Laurent; Abel, Laurent |
| 2016 | X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency Clinical Features and Novel BTK Mutations | 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; Salih Alj, Hanane; Boukari, Rachida; Bejaoui, Mohamed; Najib, Jilali; Barbouche, Mohamed-Ridha; Lau, Yu-Lung; Mellouli, Fethi; Bousfiha, Ahmed Aziz |
