Ahmed A. Bousfiha

Casablanca, Morocco

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 130 publications

Wiskott-Aldrich syndrome: clinical, immunological, and genetic characterization of the first Moroccan cohort.

Wiskott-Aldrich syndrome: clinical, immunological, and genetic characterization of the first Moroccan cohort.

Journal: Frontiers in pediatrics
Published: June 13, 2026

Auto-antibodies neutralizing type I interferons in ~10% of Moroccan patients with life-threatening COVID-19.

Auto-antibodies neutralizing type I interferons in ~10% of Moroccan patients with life-threatening COVID-19.

Journal: Frontiers in immunology
Published: May 01, 2026

Case Report: A novel homozygous splice-site variant in the C3 gene causing complete complement C3 deficiency in two unrelated Moroccan patients.

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

Genetic and autoimmune predispositions to fulminant viral hepatitis in children.

Genetic and autoimmune predispositions to fulminant viral hepatitis in children.

Journal: Frontiers in immunology
Published: April 17, 2026

Designing an integrated data model for prospective genotype-phenotype in inborn errors of immunity research.

Designing an integrated data model for prospective genotype-phenotype in inborn errors of immunity research.

Journal: Frontiers in immunology
Published: March 25, 2026

Major histocompatibility complex class II deficiency in Morocco: a 26-year retrospective cohort study.

Major histocompatibility complex class II deficiency in Morocco: a 26-year retrospective cohort study.

Journal: Frontiers in immunology
Published: March 16, 2026

Cytotoxic T-Lymphocyte-Associated Protein 4 (CTLA-4): Between immune tolerance and genetic predisposition to Systemic Lupus Erythematosus (SLE).

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

Chronic granulomatous disease: A multicenter study from the MENA region.

Chronic granulomatous disease: A multicenter study from the MENA region.

Journal: Journal of human immunity
Published: February 10, 2026

Case Report: Different faces of LRBA deficiency in five Moroccan families.

Case Report: Different faces of LRBA deficiency in five Moroccan families.

Journal: Frontiers in immunology
Published: February 09, 2026

From T-cell defect to tumorigenesis: Epstein-Barr virus-associated smooth muscle tumors in ITK deficiency.

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

Autoimmunity and inborn errors of immunity: a complex coexistence.

Autoimmunity and inborn errors of immunity: a complex coexistence.

Journal: Frontiers in immunology
Published: January 14, 2026

STAT2 R148 variant: A 16th-century founder mutation and clinical response to high-dose JAK inhibitor therapy.

STAT2 R148 variant: A 16th-century founder mutation and clinical response to high-dose JAK inhibitor therapy.

Journal: Journal of human immunity
Published: January 01, 2026
Showing 1-12 of 130

Last Updated: 09/26/2026