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Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency.
J Clin Invest. 2021 Jan 4;131(1):e139980. doi: 10.1172/JCI139980.
J Clin Invest. 2021.
PMID: 32960813
Free PMC article.
Immunologic Heterogeneity in 2 Cartilage-Hair Hypoplasia Patients With a Distinct Clinical Course.
Gamliel A, Lee YN, Lev A, AbuZaitun O, Rechavi E, Levy S, Simon AJ, Somech R.
Gamliel A, et al. Among authors: abuzaitun o.
J Investig Allergol Clin Immunol. 2023 Jul 27;33(4):263-270. doi: 10.18176/jiaci.0792. Epub 2022 Feb 15.
J Investig Allergol Clin Immunol. 2023.
PMID: 35166674
Free article.
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Whole exome sequencing (WES) approach for diagnosing primary immunodeficiencies (PIDs) in a highly consanguineous community.
Simon AJ, Golan AC, Lev A, Stauber T, Barel O, Somekh I, Klein C, AbuZaitun O, Eyal E, Kol N, Unal E, Amariglio N, Rechavi G, Somech R.
Simon AJ, et al. Among authors: abuzaitun o.
Clin Immunol. 2020 May;214:108376. doi: 10.1016/j.clim.2020.108376. Epub 2020 Mar 3.
Clin Immunol. 2020.
PMID: 32135276
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