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 by Ahmed Aziz Bousfiha, Ahmed Aziz Bousfiha, Ahmed Aziz Bousfiha, Ahmed Aziz Bousfiha, Carla Duff, Carla Duff, Carla Duff, Carla Duff, Elena Hsieh, Elena Hsieh

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

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

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Le déficit immunitaire humoral: mieux le connaître pour mieux le prendre en charge by Jalila El Bakkouri, Zahra Aadam, Fatima Ailal, Hanane Salih Alj, Ahmed Aziz Bousfiha

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

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Inborn errors of immunity and related microbiome by Raja Hazime, Raja Hazime, Fatima-Ezzohra Eddehbi, Saad El Mojadili, Nadia Lakhouaja, Ikram Souli, Abdelmouïne Salami, Bouchra M’Raouni, Imane Brahim, Mohamed Oujidi, Morad Guennouni, Ahmed Aziz Bousfiha, Ahmed Aziz Bousfiha, Brahim Admou, Brahim Admou

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HPV-Related Skin Phenotypes in Patients with Inborn Errors of Immunity by Assiya El Kettani, Fatima Ailal, Jalila El Bakkouri, Khalid Zerouali, Vivien Béziat, Emmanuelle Jouanguy, Jean-Laurent Casanova, Ahmed Aziz Bousfiha

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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 by Zineb Jouhadi, Marie Francoise Odou, Farid Zerimech, Ahmed Aziz Bousfiha, Nabiha Mikou, Nicole Porchet, Michel Crepin, Jilali Najib, Malika Balduyck

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Primary Immunodeficiencies: A Decade of Progress and a Promising Future by Isabelle Meyts, Isabelle Meyts, Aziz Bousfiha, Aziz Bousfiha, Carla Duff, Carla Duff, Surjit Singh, Surjit Singh, Surjit Singh, Yu Lung Lau, Antonio Condino-Neto, Antonio Condino-Neto, Antonio Condino-Neto, Antonio Condino-Neto, Liliana Bezrodnik, Liliana Bezrodnik, Adli Ali, Mehdi Adeli, Mehdi Adeli, Jose Drabwell

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Clinical Features of Dermatomyositis Associated with Myositis-Specific Antibodies in Moroccan Patients by Milouda Chihi, Leila Barakat, Fatima Zahra Benhayoun, Abire Allaoui, Samy Housbane, Mina Moudatir, Fouzia Hali, Ahmed Aziz Bousfiha, Jalila El Bakkouri

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

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

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Mendelian susceptibility to mycobacterial disease: an overview by Abderrahmane Errami, Jamila El Baghdadi, Fatima Ailal, Ibtihal Benhsaien, Kaoutar Ouazahrou, Laurent Abel, Jean-Laurent Casanova, Stephanie Boisson-Dupuis, Jacinta Bustamante, Ahmed Aziz Bousfiha

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Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case report by Zakaria Kasmi, Imane Ain El Hayat, Zahra Aadam, Abderrahmane Errami, Ibtihal Benhsaien, Jalila EL Bakkouri, Dalal Ben Sabbahia, Meryem Atrassi, Ahmed Aziz Bousfiha, Fatima Ailal

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Correction: Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case report by Zakaria Kasmi, Imane Ain El Hayat, Zahra Aadam, Abderrahmane Errami, Ibtihal Benhsaien, Jalila EL Bakkouri, Dalal Ben Sabbahia, Meryem Atrassi, Ahmed Aziz Bousfiha, Fatima Ailal

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

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A novel homozygous p.R1105X mutation of the AP4E1 gene in twins with hereditary spastic paraplegia and mycobacterial disease. by Xiao-Fei Kong, Aziz Bousfiha, Abdelfettah Rouissi, Yuval Itan, Avinash Abhyankar, Vanessa Bryant, Satoshi Okada, Fatima Ailal, Jacinta Bustamante, Jean-Laurent Casanova, Jennifer Hirst, Stéphanie Boisson-Dupuis

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Innate immunodeficiencies: a group of primary immunodeficiencies predisposing exclusively to common diseases by Marwa Refaat, Chaymae Oujane, Halima Kholaiq, Zahra Aadam, Abderrahmane Errami, Bouchra Baghad, Soufiane Boussetta, Assiya El Kettani, Ibtihal Benhsaien, Fatima Ailal, Asmaa Drissi Bourhanbour, Jalila El Bakkouri, Ahmed Aziz Bousfiha

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Clinical characterization of 72 patients with del(22)(q11.2q11.2) from different ethnic backgrounds by Luis A. Méndez-Rosado, Norma de León-Ojeda, Alina García, Frenny Sheth, Asmaa Gaadi, Ahmed Aziz Bousfiha, Mouna Lehlimi, Abdelhafid Natiq, Oxana S. Kurinnaia, Svetlana G. Vorsanova, Ivan Iourov, Dagmar Huhle, Thomas Liehr

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Atypical Cutaneous Viral Infections Reveal an Inborn Error of Immunity in 8 Patients by Assiya El Kettani, Fatima Ailal, Farida Marnissi, Fouzia Hali, Jalila El Bakkouri, Ibtihal Benhsaien, Tom Le Voyer, Mame Sokhna Guèye, Rémi Chevalier, Soumiya Chiheb, Khalid Zerouali, Emmanuelle Jouanguy, Jean-Laurent Casanova, Ahmed Aziz Bousfiha

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