Zahra Aadam
Casablanca, Morocco
Last Updated: 09/26/2026
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Found 20 publications
Case Report: A novel homozygous splice-site variant in the C3 gene causing complete complement C3 deficiency in two unrelated Moroccan patients.
Journal: Frontiers in immunology
Published: April 20, 2026
Cytotoxic T-Lymphocyte-Associated Protein 4 (CTLA-4): Between immune tolerance and genetic predisposition to Systemic Lupus Erythematosus (SLE).
Journal: Journal of translational autoimmunity
Published: February 25, 2026
From T-cell defect to tumorigenesis: Epstein-Barr virus-associated smooth muscle tumors in ITK deficiency.
Journal: Clinical and experimental immunology
Published: January 17, 2026
Case Report: IL2RA (CD25) deficiency: first reported cases in Morocco.
Journal: Frontiers in immunology
Published: November 24, 2025
Case Report: A novel CIITA mutation causing MHC class II deficiency: first reported case in Morocco.
Case Report: A novel CIITA mutation causing MHC class II deficiency: first reported case in Morocco.
Journal: Frontiers in immunology
Published: September 17, 2025
Levels of IL-1β and IL-1 receptor antagonist (IL-1Ra) in Moroccan children admitted to the pediatric emergency department for febrile seizures.
Journal: BMC pediatrics
Published: July 12, 2025
Molecular characterization of extended spectrum beta-lactamase-producing Enterobacterales from urinary tract infections in Burundi.
Journal: BMC infectious diseases
Published: July 11, 2025
Defects in Innate and Intrinsic Immunity in Morocco: A Retrospective Analysis of the Genetic Landscape and Clinical Correlations.
Journal: Pathogens & immunity
Published: June 05, 2025
Autoimmune manifestations in children with inborn errors of immunity in Morocco: A study from the national registry.
Journal: Journal of translational autoimmunity
Published: April 30, 2025
Correction: Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case report.
Journal: BMC medical genomics
Published: February 03, 2025
Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case report.
Journal: BMC medical genomics
Published: August 29, 2024
Major Histocompatibility Complex Class II Deficiency Beyond Infancy.
Journal: Case reports in immunology
Published: July 23, 2024
Last Updated: 09/26/2026