Syndrome d’activation macrophagique compliquant une lymphohistiocytose familiale

por Boussaadni, Yousra El, Benajiba, Noufissa, Bousfiha, Ahmed Aziz, Ailal, Fatima
Publicado 2017

Le déficit immunitaire humoral: mieux le connaître pour mieux le prendre en charge

por El Bakkouri, Jalila, Aadam, Zahra, Ailal, Fatima, Alj, Hanane Salih, Bousfiha, Ahmed Aziz
Publicado 2014

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

Érythrodermie néonatale: ne pas méconnaitre un déficit immunitaire

por El Ouali, Aziza, El Boussaadni, Yousra, Ailal, Fatima, Bousfiha, Ahmed Aziz, Dikhaye, Sihame, Benajiba, Noufissa
Publicado 2014

Quand faut il suspecter un déficit immunitaire chez l’adulte?

por Allaoui, Abire, Mokhantar, Khaoula, Jeddane, Leila, Ailal, Fatima, Elkabli, Hassan, Bousfiha, Ahmed Aziz, Moudatir, Mina
Publicado 2022

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

Classification of common variable immunodeficiency through immunological and clinical phenotyping in Moroccan patients

por Mokhantar, Khaoula, Allaoui, Abir, Ailal, Fatima, Bakkouri, Jalila El, Ouazahrou, Kaoutar, Errami, Abderrahmane, Bousfiha, Ahmed Aziz, Moudatir, Mina
Publicado 2023

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

HPV-Related Skin Phenotypes in Patients with Inborn Errors of Immunity

por El Kettani, Assiya, Ailal, Fatima, El Bakkouri, Jalila, Zerouali, Khalid, Béziat, Vivien, Jouanguy, Emmanuelle, Casanova, Jean-Laurent, 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

Homozygous STAT2 gain-of-function mutation by loss of USP18 activity in a patient with type I interferonopathy

por Gruber, Conor, Martin-Fernandez, Marta, Ailal, Fatima, Qiu, Xueer, Taft, Justin, Altman, Jennie, Rosain, Jérémie, Buta, Sofija, Bousfiha, Aziz, Casanova, Jean-Laurent, Bustamante, Jacinta, Bogunovic, Dusan
Publicado 2020

A Novel Homozygous p.R1105X Mutation of the AP4E1 Gene in Twins with Hereditary Spastic Paraplegia and Mycobacterial Disease

por Kong, Xiao-Fei, Bousfiha, Aziz, Rouissi, Abdelfettah, Itan, Yuval, Abhyankar, Avinash, Bryant, Vanessa, Okada, Satoshi, Ailal, Fatima, Bustamante, Jacinta, Casanova, Jean-Laurent, Hirst, Jennifer, Boisson-Dupuis, Stéphanie
Publicado 2013

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

Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification

por Bousfiha, Aziz, Jeddane, Leila, Picard, Capucine, Al-Herz, Waleed, Ailal, Fatima, Chatila, Talal, Cunningham-Rundles, Charlotte, Etzioni, Amos, Franco, Jose Luis, Holland, Steven M, Klein, Christoph, Morio, Tomohiro, Ochs, Hans D., Oksenhendler, Eric, Puck, Jennifer, Torgerson, Troy R., Casanova, Jean-Laurent, Sullivan, Kathleen E., Tangye, Stuart G.
Publicado 2020

The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies

por Bousfiha, Aziz, Jeddane, Leïla, Al-Herz, Waleed, Ailal, Fatima, Casanova, Jean‐Laurent, Chatila, Talal, Conley, Mary Ellen, Cunningham‐Rundles, Charlotte, Etzioni, Amos, Franco, Jose Luis, Gaspar, H. Bobby, Holland, Steven M., Klein, Christoph, Nonoyama, Shigeaki, Ochs, Hans D., Oksenhendler, Eric, Picard, Capucine, Puck, Jennifer M., Sullivan, Kathleen E., Tang, Mimi L. K.
Publicado 2015

The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies

por Bousfiha, Aziz, Jeddane, Leïla, Picard, Capucine, Ailal, Fatima, Bobby Gaspar, H., Al-Herz, Waleed, Chatila, Talal, Crow, Yanick J., Cunningham-Rundles, Charlotte, Etzioni, Amos, Franco, Jose Luis, Holland, Steven M., Klein, Christoph, Morio, Tomohiro, Ochs, Hans D., Oksenhendler, Eric, Puck, Jennifer, Tang, Mimi L. K., Tangye, Stuart G., Torgerson, Troy R., Casanova, Jean-Laurent, Sullivan, Kathleen E.
Publicado 2017

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

Dual T cell– and B cell–intrinsic deficiency in humans with biallelic RLTPR mutations

por Wang, Yi, Ma, Cindy S., Ling, Yun, Bousfiha, Aziz, Camcioglu, Yildiz, Jacquot, Serge, Payne, Kathryn, Crestani, Elena, Roncagalli, Romain, Belkadi, Aziz, Kerner, Gaspard, Lorenzo, Lazaro, Deswarte, Caroline, Chrabieh, Maya, Patin, Etienne, Vincent, Quentin B., Müller-Fleckenstein, Ingrid, Fleckenstein, Bernhard, Ailal, Fatima, Quintana-Murci, Lluis, Fraitag, Sylvie, Alyanakian, Marie-Alexandra, Leruez-Ville, Marianne, Picard, Capucine, Puel, Anne, Bustamante, Jacinta, Boisson-Dupuis, Stéphanie, Malissen, Marie, Malissen, Bernard, Abel, Laurent, Hovnanian, Alain, Notarangelo, Luigi D., Jouanguy, Emmanuelle, Tangye, Stuart G., Béziat, Vivien, Casanova, Jean-Laurent
Publicado 2016

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

Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome

por Kreins, Alexandra Y., Ciancanelli, Michael J., Okada, Satoshi, Kong, Xiao-Fei, Ramírez-Alejo, Noé, Kilic, Sara Sebnem, El Baghdadi, Jamila, Nonoyama, Shigeaki, Mahdaviani, Seyed Alireza, Ailal, Fatima, Bousfiha, Aziz, Mansouri, Davood, Nievas, Elma, Ma, Cindy S., Rao, Geetha, Bernasconi, Andrea, Sun Kuehn, Hye, Niemela, Julie, Stoddard, Jennifer, Deveau, Paul, Cobat, Aurelie, El Azbaoui, Safa, Sabri, Ayoub, Lim, Che Kang, Sundin, Mikael, Avery, Danielle T., Halwani, Rabih, Grant, Audrey V., Boisson, Bertrand, Bogunovic, Dusan, Itan, Yuval, Moncada-Velez, Marcela, Martinez-Barricarte, Ruben, Migaud, Melanie, Deswarte, Caroline, Alsina, Laia, Kotlarz, Daniel, Klein, Christoph, Muller-Fleckenstein, Ingrid, Fleckenstein, Bernhard, Cormier-Daire, Valerie, Rose-John, Stefan, Picard, Capucine, Hammarstrom, Lennart, Puel, Anne, Al-Muhsen, Saleh, Abel, Laurent, Chaussabel, Damien, Rosenzweig, Sergio D., Minegishi, Yoshiyuki, Tangye, Stuart G., Bustamante, Jacinta, Casanova, Jean-Laurent, Boisson-Dupuis, Stéphanie
Publicado 2015