Area of research
Immunology · Genetics · Iranian Registry
Research interest
Research interests include Immunodeficiency and Autoimmune Disorders, Blood disorders and treatments, Immune Cell Function and Interaction, and T-cell and B-cell Immunology.
Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients
Evaluation of Expression of LRBA and CTLA-4 Proteins in Common Variable Immunodeficiency Patients.
The First Iranian Cohort of Pediatric Patients with Activated Phosphoinositide 3-Kinase-δ (PI3Kδ) Syndrome (APDS).
Protein Kinase C-Delta Defect in Autoimmune Lymphoproliferative Syndrome-Like Disease: First Case from the National Iranian Registry and Review of the Literature.
Primary Immunodeficiency and Thrombocytopenia.
Protein Kinase C-Delta Defect in Autoimmune Lymphoproliferative Syndrome-Like Disease: First Case from the National Iranian Registry and Review of the Literature.
Consensus Middle East and North Africa Registry on Inborn Errors of Immunity
International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome
Clinical, immunological, and genetic features in 780 patients with autoimmune lymphoproliferative syndrome (ALPS) and ALPS‐like diseases: A systematic review
Clinical, immunological, and genetic features in 780 patients with autoimmune lymphoproliferative syndrome (ALPS) and ALPS-like diseases: A systematic review.
Effect of Class Switch Recombination Defect on the Phenotype of Ataxia-Telangiectasia Patients.
The spectrum of ATM gene mutations in Iranian patients with ataxia-telangiectasia.
Known and potential molecules associated with altered B cell development leading to predominantly antibody deficiencies.
Lymphocytes subsets in correlation with clinical profile in CVID patients without monogenic defects.
Evaluation of Radiation Sensitivity in Patients with Hyper IgM Syndrome.
Application of Flow Cytometry in Predominantly Antibody Deficiencies.
The urgent need for integrated science to fight COVID-19 pandemic and beyond
Global systematic review of primary immunodeficiency registries
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations
Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency
Primary Immunodeficiency Diseases and Bacillus Calmette-Guérin (BCG)-Vaccine–Derived Complications: A Systematic Review
Ataxia-telangiectasia: epidemiology, pathogenesis, clinical phenotype, diagnosis, prognosis and management
Ataxia-telangiectasia: epidemiology, pathogenesis, clinical phenotype, diagnosis, prognosis and management.
Clinical, Immunological, and Genetic Features in 49 Patients With ZAP-70 Deficiency: A Systematic Review
Autoimmunity in common variable immunodeficiency: a systematic review and meta-analysis.
A new case of congenital ficolin-3 deficiency with primary immunodeficiency.
Agammaglobulinemia: Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management.
Leishmaniasis and Autoimmunity in Patient with LPS-Responsive Beige-Like Anchor Protein (LRBA) Deficiency.
Ataxia‐telangiectasia: A review of clinical features and molecular pathology
Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score