Severe Combined Immunodeficiency Disorder due to a Novel Mutation in Recombination Activation Gene 2: About 2 Cases

por Benhsaien, Ibtihal, Ailal, Fatima, Elazhary, Khadija, El bakkouri, Jalila, Badou, Abdallah, Bousfiha, Ahmed Aziz
Publicado 2021

Chronic upper airway inflammation related to high Th2 cytokines in Mendelian susceptibility to mycobacterial disease case

por Benhsaien, Ibtihal, Yang, Rui, Ailal, Fatima, Weisshaar, Marc, Mele, Federico, Casanova, Jean-Laurent, Bustamante, Jacinta, Bousfiha, Ahmed
Publicado 2022

Syndrome lymphoprolifératif avec autoimmunité: à propos d’un cas

por Youssif, Houda Ben, Ailal, Fatima, Benhsaien, Ibtihal, Bakkouri, Jalila El, Jeddane, Laila, Maani, Khadija El, Bousfiha, Ahmed Aziz
Publicado 2022

Le profil clinique et immunologique de 15 patients Marocains atteints de syndrome hyper IgM

por Ouair, Hind, Benhsaien, Ibtihal, Jeddane, Leila, El Bakkouri, Jalila, Elhafidi, Naima, Rada, Noureddine, Najib, Jilali, Ailal, Fatima, Alj, Hanane Salih, Bousfiha, Ahmed Aziz
Publicado 2017

Atypical Cutaneous Viral Infections Reveal an Inborn Error of Immunity in 8 Patients

por El Kettani, Assiya, Ailal, Fatima, Marnissi, Farida, Hali, Fouzia, El Bakkouri, Jalila, Benhsaien, Ibtihal, Le Voyer, Tom, Guèye, Mame Sokhna, Chevalier, Rémi, Chiheb, Soumiya, Zerouali, Khalid, Jouanguy, Emmanuelle, Casanova, Jean-Laurent, Bousfiha, Ahmed Aziz
Publicado 2023

High Th2 cytokine levels and upper airway inflammation in human inherited T-bet deficiency

por Yang, Rui, Weisshaar, Marc, Mele, Federico, Benhsaien, Ibtihal, Dorgham, Karim, Han, Jing, Croft, Carys A., Notarbartolo, Samuele, Rosain, Jérémie, Bastard, Paul, Puel, Anne, Fleckenstein, Bernhard, Glimcher, Laurie H., Di Santo, James P., Ma, Cindy S., Gorochov, Guy, Bousfiha, Aziz, Abel, Laurent, Tangye, Stuart G., Casanova, Jean-Laurent, Bustamante, Jacinta, Sallusto, Federica
Publicado 2021

A partial form of inherited human USP18 deficiency underlies infection and inflammation

por Martin-Fernandez, Marta, Buta, Sofija, Le Voyer, Tom, Li, Zhi, Dynesen, Lasse Toftdal, Vuillier, Françoise, Franklin, Lina, Ailal, Fatima, Muglia Amancio, Alice, Malle, Louise, Gruber, Conor, Benhsaien, Ibtihal, Altman, Jennie, Taft, Justin, Deswarte, Caroline, Roynard, Manon, Nieto-Patlan, Alejandro, Moriya, Kunihiko, Rosain, Jérémie, Boddaert, Nathalie, Bousfiha, Aziz, Crow, Yanick J., Jankovic, Dragana, Sher, Alan, Casanova, Jean-Laurent, Pellegrini, Sandra, Bustamante, Jacinta, Bogunovic, Dusan
Publicado 2022

Human T-bet governs the generation of a distinct subset of CD11c(high)CD21(low) B cells

por Yang, Rui, Avery, Danielle T., Jackson, Katherine J. L., Ogishi, Masato, Benhsaien, Ibtihal, Du, Likun, Ye, Xiaofei, Han, Jing, Rosain, Jérémie, Peel, Jessica N., Alyanakian, Marie-Alexandra, Neven, Bénédicte, Winter, Sarah, Puel, Anne, Boisson, Bertrand, Payne, Kathryn J., Wong, Melanie, Russell, Amanda J., Mizoguchi, Yoko, Okada, Satoshi, Uzel, Gulbu, Goodnow, Christopher C., Latour, Sylvain, Bakkouri, Jalila El, Bousfiha, Aziz, Preece, Kahn, Gray, Paul E., Keller, Baerbel, Warnatz, Klaus, Boisson-Dupuis, Stéphanie, Abel, Laurent, Pan-Hammarström, Qiang, Bustamante, Jacinta, Ma, Cindy S., Casanova, Jean-Laurent, Tangye, Stuart G.
Publicado 2022

Human inherited complete STAT2 deficiency underlies inflammatory viral diseases

por Bucciol, Giorgia, Moens, Leen, Ogishi, Masato, Rinchai, Darawan, Matuozzo, Daniela, Momenilandi, Mana, Kerrouche, Nacim, Cale, Catherine M., Treffeisen, Elsa R., Al Salamah, Mohammad, Al-Saud, Bandar K., Lachaux, Alain, Duclaux-Loras, Remi, Meignien, Marie, Bousfiha, Aziz, Benhsaien, Ibtihal, Shcherbina, Anna, Roppelt, Anna, Gothe, Florian, Houhou-Fidouh, Nadhira, Hackett, Scott J., Bartnikas, Lisa M., Maciag, Michelle C., Alosaimi, Mohammed F., Chou, Janet, Mohammed, Reem W., Freij, Bishara J., Jouanguy, Emmanuelle, Zhang, Shen-Ying, Boisson-Dupuis, Stephanie, Béziat, Vivien, Zhang, Qian, Duncan, Christopher J.A., Hambleton, Sophie, Casanova, Jean-Laurent, Meyts, Isabelle
Publicado 2023

Disruption of an anti-mycobacterial circuit between dendritic and Th cells in human SPPL2a deficiency

por Kong, Xiao-Fei, Martinez-Barricarte, Ruben, Kennedy, James, Mele, Federico, Lazarov, Tomi, Deenick, Elissa K, Ma, Cindy S, Breton, Gaëlle, Lucero, Kimberly B, Langlais, David, Bousfiha, Aziz, Aytekin, Caner, Markle, Janet, Trouillet, Céline, Jabot-Hanin, Fabienne, Lindestam Arlehamn, Cecilia S., Rao, Geetha, Picard, Capucine, Lasseau, Théo, Latorre, Daniela, Hambleton, Sophie, Deswarte, Caroline, Itan, Yuval, Abarca, Katia, Moraes-Vasconcelos, Dewton, Ailal, Fatima, Ikinciogullari, Aydan, Dogu, Figen, Benhsaien, Ibtihal, Sette, Alessandro, Abel, Laurent, Boisson-Dupuis, Stéphanie, Schröder, Bernd, Nussenzweig, Michel C., Liu, Kang, Geissmann, Frédéric, Tangye, Stuart G., Gros, Philippe, Sallusto, Federica, Bustamante, Jacinta, Casanova, Jean-Laurent
Publicado 2018

Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia

por García-García, Ana, Pérez de Diego, Rebeca, Flores, Carlos, Rinchai, Darawan, Solé-Violán, Jordi, Deyà-Martínez, Àngela, García-Solis, Blanca, Lorenzo-Salazar, José M., Hernández-Brito, Elisa, Lanz, Anna-Lisa, Moens, Leen, Bucciol, Giorgia, Almuqamam, Mohamed, Domachowske, Joseph B., Colino, Elena, Santos-Perez, Juan Luis, Marco, Francisco M., Pignata, Claudio, Bousfiha, Aziz, Turvey, Stuart E., Bauer, Stefanie, Haerynck, Filomeen, Ocejo-Vinyals, Javier Gonzalo, Lendinez, Francisco, Prader, Seraina, Naumann-Bartsch, Nora, Pachlopnik Schmid, Jana, Biggs, Catherine M., Hildebrand, Kyla, Dreesman, Alexandra, Cárdenes, Miguel Ángel, Ailal, Fatima, Benhsaien, Ibtihal, Giardino, Giuliana, Molina-Fuentes, Agueda, Fortuny, Claudia, Madhavarapu, Swetha, Conway, Daniel H., Prando, Carolina, Schidlowski, Laire, Martínez de Saavedra Álvarez, María Teresa, Alfaro, Rafael, Rodríguez de Castro, Felipe, Meyts, Isabelle, Hauck, Fabian, Puel, Anne, Bastard, Paul, Boisson, Bertrand, Jouanguy, Emmanuelle, Abel, Laurent, Cobat, Aurélie, Zhang, Qian, Casanova, Jean-Laurent, Alsina, Laia, Rodríguez-Gallego, Carlos
Publicado 2023