Up a level |
(2023) Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population. Journal of Clinical Immunology. p. 12. ISSN 0271-9142
(2021) Autoimmune Manifestations among Patients with Monogenic Inborn Errors of Immunity. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology. ISSN 1399-3038 (Electronic) 0905-6157 (Linking)
(2021) Autoimmune manifestations among 461 patients with monogenic inborn errors of immunity. Pediatric Allergy and Immunology. p. 14. ISSN 0905-6157
(2020) Monogenic Primary Immunodeficiency Disorder Associated with Common Variable Immunodeficiency and Autoimmunity. International archives of allergy and immunology. pp. 706-714. ISSN 1423-0097 (Electronic) 1018-2438 (Linking)
(2019) Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort. Journal of Allergy and Clinical Immunology-in Practice. 864-+. ISSN 2213-2198
(2018) Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort. The journal of allergy and clinical immunology. In practice. ISSN 2213-2201 (Electronic)
(2018) Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis. Journal of Clinical Immunology. pp. 816-832. ISSN 0271-9142