O. AbuZaitun

Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency.

J. Casanova, Shen-Ying Zhang, B. Boisson, 2020, The Journal of clinical investigation.

Whole exome sequencing (WES) approach for diagnosing primary immunodeficiencies (PIDs) in a highly consanguineous community.

C. Klein, E. Eyal, N. Amariglio, 2020, Clinical immunology.

Immunologic heterogeneity in two Cartilage-Hair Hypoplasia (CHH) patients with distinct clinical course.

R. Somech, A. Lev, A. J. Simón, 2022, Journal of investigational allergology & clinical immunology.