Major Histocompatibility Complex Class II Deficiency Beyond Infancy by Aziza Bachir Kattra, Ibtihal Benhsaien, Asmaa Drissi Bourhanbour, Zahra Aadam, Abderrahmane Errami, Fatima Ailal, Ahmed Aziz Bousfiha, Jalila El Bakkouri

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Autoimmune manifestations in children with inborn errors of immunity in Morocco: A study from the national registry by Ahamada Elamine, Ibtihal Benhsaien, Fatima Ailal, Abderrahmane Errami, Zakaria Kasmi, Zahra Aadam, Asmaa Drissi Bourhanbour, Ahmed Aziz Bousfiha, Jalila El Bakkouri

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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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Clinical, immunological, and genetic landscape of common variable immunodeficiency in Morocco: a nationwide multicenter study by Abire Allaoui, Abire Allaoui, Abderrahmane Moundir, Ibtihal Benhsaien, Fatima Ailal, Jalila El Bakkouri, Khadija Echchilali, Abdelhamid Naitlho, Hassan El Kabli, Ahmed Aziz Bousfiha, Mina Moudatir

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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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