Abderrahmane Errami
Casablanca, Morocco
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 22 publications
Wiskott-Aldrich syndrome: clinical, immunological, and genetic characterization of the first Moroccan cohort.
Journal: Frontiers in pediatrics
Published: June 13, 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
ISO 9001 in hospitals: a systematic review and implementation framework for clinical services in emerging countries.
Journal: International journal for quality in health care : journal of the International Society for Quality in Health Care
Published: August 06, 2025
Rare STAT1 variants in Moroccan tuberculosis patients: insights into host genetic susceptibility.
Journal: Clinical and experimental immunology
Published: July 27, 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
STAT1 gain-of-function in 12 Moroccan patients: Clinical and genetic insights.
Journal: Journal of human immunity
Published: March 03, 2025
Arabic Translation and Adaptation of the CVID_QoL Questionnaire to Measure Health-RelatedQuality of Life of Adultswith Common Variable Immune Deficiency.
Journal: La Tunisie medicale
Published: February 10, 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