N. Benhalla

Inborn Errors of Immunity in Algerian Children and Adults: A Single-Center Experience Over a Period of 13 Years (2008–2021)

J. Casanova, Y. Lau, A. Puel, 2022, Frontiers in Immunology.

Clinical, immunological and genetic features in eleven Algerian patients with major histocompatibility complex class II expression deficiency

R. Djidjik, M. Baghriche, L. Smati, 2012, Allergy, Asthma & Clinical Immunology.

F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects.

L. Notarangelo, R. Geha, J. Chou, 2019, The Journal of allergy and clinical immunology.

Prevalence of BTK mutations in male Algerian patterns with agammaglobulinemia and severe B cell lymphopenia.

Y. Lau, F. Magdinier, Koon-wing Chan, 2015, Clinical immunology.

[Common variable immunodeficiency (CVID): clinical and immunological features of 29 Algerian patients].

N. Zidouni, R. Djidjik, M. Gharnaout, 2014, Pathologie-biologie.

Prevalence of BTK mutations in male Algerian patterns with agammaglobulinemia and severe B cell lymphopenia.

Y. Lau, F. Magdinier, Koon-wing Chan, 2015, Clinical immunology.