Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic reviewParisa Amirifar, Reza Yazdani, Mohammad Reza Ranjouri et al.|Pediatric Allergy and Immunology|2020Cited by 28
The first cohort of Iranian patients with hyper immunoglobulin E syndrome: A long‐term follow‐up and genetic analysisMahmood Tavassoli, Asghar Aghamohammadi, Mohsen Ghadami et al.|Pediatric Allergy and Immunology|2019Cited by 26
Autoimmune manifestations among 461 patients with monogenic inborn errors of immunityGholamreza Azizi, Ahmad Vosughimotlagh, Marzieh Tavakol et al.|Pediatric Allergy and Immunology|2021Cited by 20
B cells and T cells abnormalities in patients with selective IgA deficiencyYasser Bagheri, Reza Yazdani, Tannaz Moeini Shad et al.|Allergy Asthma and Clinical Immunology|2023Cited by 11
Evaluation of patients with primary immunodeficiency associated with Bacille Calmette-Guerin (BCG)-vaccine-derived complicationsMahsa Sohani, Asghar Aghamohammadi, S Habibi et al.|Allergologia et Immunopathologia|2020Cited by 8