| A new case of congenital ficolin-3 deficiency with primary immunodeficiency F Babaha, H Abolhassani, Z Hamidi Esfahani, R Yazdani, ... Expert review of clinical immunology 16 (7), 733-738, 2020 | 11 | 2020 |
| Evaluation of miR-210 expression in common variable immunodeficiency: patients with unsolved genetic defect F Babaha, R Yazdani, S Shahkarami, ZH Esfahani, H Abolhahassani, ... Allergologia et Immunopathologia 49 (2), 84-93, 2021 | 10 | 2021 |
| PIK3R1 Mutation Associated with Hyper IgM (APDS2 Syndrome): A Case Report and Review of the Literature R Yazdani, Z Hamidi, F Babaha, A Gholamreza, S Fekrvand, ... Endocr Metab Immune Disord Drug Targets 19 (7), 941-958, 2019 | 7 | 2019 |
| Evaluation of microRNA-125b-5p and transcription factors BLIMP1 and IRF4 expression in unsolved common variable immunodeficiency patients ZH Esfahani, R Yazdani, S Shahkarami, F Babaha, H Abolhassani, ... Iranian Journal of Allergy, Asthma and Immunology 20 (6), 700-710, 2021 | 5 | 2021 |
| ATM Expression and Activation in Ataxia Telangiectasia Patients with and without Class Switch Recombination Defects F Salami, TM Shad, N Fathi, H Mojtahedi, M Esmaeili, S Shahkarami, ... Journal of Clinical Immunology 45 (1), 67, 2025 | | 2025 |
| Cancer Trends in Inborn Errors of Immunity: A Systematic Review and Meta-Analysis S Fekrvand, H Abolhassani, ZH Esfahani, NNG Fard, M Amiri, H Salehi, ... Journal of Clinical Immunology 45 (1), 34, 2025 | | 2025 |
