Omenn syndrome caused by a novel homozygous mutation in recombination activating gene 1 von Benhsaien, Ibtihal, Essadssi, Soukaina, Elkhattabi, Lamiae, Bakhchane, Amina, Abdelghaffar, Houria, Bousfiha, Ahmed Aziz, Badou, Abdallah, Barakat, Abdelhamid

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Global systematic review of primary immunodeficiency registries von Abolhassani, H, Azizi, G, Sharifi, L, Yazdani, R, Mohsenzadegan, M, Delavari, S, Sohani, M, Shirmast, P, Zahra, Mahdaviani, SA, Kalantari, A, Tavakol, M, Jabbari-Azad, F, Ahanchian, H, Momen, T, Sherkat, R, Sadeghi-Shabestari, M, Aleyasin, S, Esmaeilzadeh, H, Al-Herz, W, Bousfiha, AA, Condino-Neto, A, Seppanen, M, Sullivan, KE, Hammarstrom, L, Modell, V, Modell, F, Quinn, J, Orange, JS, Aghamohammadi, A

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The Seven STAT3-Related Hyper-IgE Syndromes von Fadil, Ilham, Ben-Ali, Meriem, Jeddane, Leila, Barbouche, Mohamed-Ridha, Bousfiha, Ahmed Aziz

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Alpha1 antitrypsin deficiency due to an homozygous PI Null Q0Cairo mutation: Early onset of pulmonary manifestations and variability of clinical expression von Jouhadi, Zineb, Odou, Marie Francoise, Zerimech, Farid, Bousfiha, Ahmed Aziz, Mikou, Nabiha, Porchet, Nicole, Crepin, Michel, Najib, Jilali, Balduyck, Malika

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Ensuring Access to Immunoglobulin Therapies for People with Primary Immunodeficiency: A Need to Improve Individuals' Quality of Life and the Sustainability of Health-care Systems von Bousfiha, Ahmed Aziz, Duff, Carla, Hsieh, Elena

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A Homozygous RAG1 Gene Mutation in a Case of Combined Immunodeficiency: Clinical, Molecular, and Computational Analysis von Essadssi, Soukaina, Benhsaien, Ibtihal, Bakhchane, Amina, Charoute, Hicham, Abdelghaffar, Houria, Bousfiha, Ahmed Aziz, Barakat, Abdelhamid

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Case Report of Two Independent Moroccan Families with Syndromic Epidermodysplasia Verruciformis and STK4 Deficiency von El Kettani, Assiya, Ouair, Hind, Marnissi, Farida, El Bakkouri, Jalila, Chevalier, Rémi, Lorenzo, Lazaro, Kholaiq, Halima, Béziat, Vivien, Jouanguy, Emmanuelle, Casanova, Jean-Laurent, Bousfiha, Ahmed Aziz

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Efficacy of Anakinra Treatment in two Moroccan Patients With Mevalonate Kinase Deficiency von Souali, Manal, Sakhi, Asmaa, Bousfiha, Ahmed Aziz, Bouayed, Kenza

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Primary Immunodeficiency Classification on Smartphone von Jeddane, Leïla, Ouair, Hind, Benhsaien, Ibtihal, Bakkouri, Jalila El, Bousfiha, Ahmed Aziz

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Clinical and Immunological Features of 96 Moroccan Children with SCID Phenotype: Two Decades’ Experience von Benhsaien, Ibtihal, Ailal, Fatima, El Bakkouri, Jalila, Jeddane, Leïla, Ouair, Hind, Admou, Brahim, Bouskraoui, Mohamed, Hbibi, Mohamed, Hida, Mustapha, Amenzoui, Naïma, Jouhadi, Zineb, El Hafidi, Naïma, Rada, Nouredine, Benajiba, Noufissa, Abilkassem, Rachid, Badou, Abdallah, Bousfiha, Ahmed Aziz

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Innate immunodeficiencies: a group of primary immunodeficiencies predisposing exclusively to common diseases von Refaat, Marwa, Oujane, Chaymae, Kholaiq, Halima, Aadam, Zahra, Errami, Abderrahmane, Baghad, Bouchra, Boussetta, Soufiane

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Exploring inflammatory markers of COVID-19 severity in Moroccans von Drissi Bourhanbour, Asmaa, Kattra, Aziza Bachir, Aissaoui, Ouissal, Ouair, Hind, Benzekri, Driss, Kholaiq, Halima, Charra, Boubaker, Jalila, El Bakkouri, Bousfiha, Ahmed Aziz

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Chronic mucocutaneous candidiasis with severe oral injury associated with a STAT 1 gain-of-function mutation von Mahad, Chaimae, Baghad, Bouchra, Bousfiha, Ahmed Aziz, Puel, Anne, Benyahya, Ihsane

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Severe Combined Immunodeficiency Disorder due to a Novel Mutation in Recombination Activation Gene 2: About 2 Cases von Benhsaien, Ibtihal, Ailal, Fatima, Elazhary, Khadija, El bakkouri, Jalila, Badou, Abdallah, Bousfiha, Ahmed Aziz

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

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Syndrome d’activation macrophagique compliquant une lymphohistiocytose familiale von Boussaadni, Yousra El, Noufissa, Benajiba, Bousfiha Ahmed Aziz, Ailal Fatima

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The International Alliance of Primary Immune Deficiency Societies von Gennery, Andrew R., Abraham, Roshini S., Torgerson, Troy R., Etzioni, Amos, Cant, Andrew J., Meyts, Isabelle, Chipeta, James, Bousfiha, Ahmed Aziz, Dieye, Tandakha D., Condino-Neto, Antonio, Espinosa, Francisco, Besrodnik, Liliana, Lau, Yu-Lung, Singh, Surjit, Chan, Godfrey C. F., Orange, Jordan S.

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Clinical characterization of 72 patients with del from different ethnic backgrounds von Méndez-Rosado, Luis A, de León-Ojeda, Norma, García, Alina, Sheth, Frenny, Gaadi, Asmaa, Bousfiha, Ahmed Aziz, Lehlimi, Mouna

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The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population von Naamane, Hamid, El Maataoui, Ouafaa, Ailal, Fatima, Barakat, Abdelhamid, Bennani, Siham, Najib, Jilali, Hassar, Mohammed, Saile, Rachid, Bousfiha, Ahmed Aziz

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Le profil clinique et immunologique de 15 patients Marocains atteints de syndrome hyper IgM von Ouair Hind, Benhsaien Ibtihal, Jeddane Leila, Jalila, El Bakkouri, Elhafidi Naima, Rada Noureddine, Jilali, Najib, Ailal Fatima, Alj Hanane Salih, Bousfiha Ahmed Aziz

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