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Clinical heterogeneity in families with multiple cases of inborn errors of immunity.
Delavari S, Rasouli SE, Fekrvand S, Chavoshzade Z, Mahdaviani SA, Shirmast P, Sharafian S, Sherkat R, Momen T, Aleyasin S, Ahanchian H, Sadeghi-Shabestari M, Esmaeilzadeh H, Barzamini S, Tarighatmonfared F, Salehi H, Esmaeili M, Marzani Z, Fathi N, Abolnezhadian F, Rad MK, Saeedi-Boroujeni A, Shirkani A, Bagheri Z, Salami F, Shad TM, Marzbali MY, Mojtahedi H, Razavi A, Tavakolinia N, Cheraghi T, Tavakol M, Shafiei A, Behniafard N, Ebrahimi SS, Sepahi N, Ghaneimoghadam A, Rezaei A, Kalantari A, Abolhassani H, Rezaei N. Delavari S, et al. Among authors: fekrvand s. Clin Immunol. 2024 Feb;259:109896. doi: 10.1016/j.clim.2024.109896. Epub 2024 Jan 4. Clin Immunol. 2024. PMID: 38184287
Role of rare immune cells in common variable immunodeficiency.
Soltani M, Rezaei M, Fekrvand S, Ganjalikhani-Hakemi M, Abolhassani H, Yazdani R. Soltani M, et al. Among authors: fekrvand s. Pediatr Allergy Immunol. 2022 Feb;33(2):e13725. doi: 10.1111/pai.13725. Pediatr Allergy Immunol. 2022. PMID: 34937129 Review.
The First Iranian Cohort of Pediatric Patients with Activated Phosphoinositide 3-Kinase-δ (PI3Kδ) Syndrome (APDS).
Fekrvand S, Delavari S, Chavoshzadeh Z, Sherkat R, Mahdaviani SA, Sadeghi Shabestari M, Azizi G, Arzanian MT, Shahin Shamsian B, Eskandarzadeh S, Eslami N, Rae W, Condino-Neto A, Mohammadi J, Abolhassani H, Yazdani R, Aghamohammadi A. Fekrvand S, et al. Immunol Invest. 2022 Apr;51(3):644-659. doi: 10.1080/08820139.2020.1863982. Epub 2021 Jan 6. Immunol Invest. 2022. PMID: 33401995
21 results