Tehran University of Medical Sciences

Science Communicator Platform

Faculty Members have conducted research related to the Mutations in Gjb2 As Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of C.299-300Delat Mutation in Kurdish Population of Iran
Anahita Razaghian

Assistant Professor of Allergy and Clinical Immunology

Department Pediatrics

School of Medicine

Hakim Children Hospital

Tehran University of Medical Sciences

All Documents
1. A Cohort Study of 38 Classic Wiskott-Aldrich Syndrome Cases With Six Novel Mutations, Journal of Clinical Immunology (2026)
2. Atopic March in a Case of Filaggrin Gene Mutation, Pediatric, Allergy, Immunology, and Pulmonology (2025)
3. Clinical Characterization and Mutation Analysis of 13 Iranian Ataxia Telangiectasia Patients: Introducing Two Novel Mutations, Iranian journal of allergy, asthma, and immunology (2025)
4. Diverse Phenotypic Expressions of Ada2 Deficiency: Two Case Studies, Iranian Journal of Allergy, Asthma and Immunology (2025)
5. Early Diagnosis of Immunodeficient Patients With Partial Albinism: The Role of Hair Study and Peripheral Blood Smear, Pediatric Allergy and Immunology (2024)
6. Clinical and Immunological Characteristics of 69 Leukocyte Adhesion Deficiency-I Patients, Pediatric Allergy and Immunology (2023)
7. Clinical and Immunological Characteristics of 69 Leukocyte Adhesion Deficiency-I Patients, Pediatric Allergy and Immunology (2023)
8. Tumor Necrosis Factor-Α (-308G>A) Gene Polymorphism and Its Association With Asthma and Atopy Status, Iranian Journal of Allergy# Asthma and Immunology (2023)
9. Autoimmune Manifestations Among 461 Patients With Monogenic Inborn Errors of Immunity, Pediatric Allergy and Immunology (2021)
10. Autoimmune Manifestations Among 461 Patients With Monogenic Inborn Errors of Immunity, Pediatric Allergy and Immunology (2021)
11. Evaluation of Respiratory Complications in Patients With X-Linked and Autosomal Recessive Agammaglobulinemia, Pediatric Allergy and Immunology (2020)
12. Griscelli Syndrome Type 2 Sine Albinism: Unraveling Differential Rab27a Effector Engagement, Frontiers in Immunology (2020)
13. Monogenic Primary Immunodeficiency Disorder Associated With Common Variable Immunodeficiency and Autoimmunity, International Archives of Allergy and Immunology (2020)
14. Monogenic Primary Immunodeficiency Disorder Associated With Common Variable Immunodeficiency and Autoimmunity, International Archives of Allergy and Immunology (2020)
15. Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort, Journal of Allergy and Clinical Immunology: In Practice (2019)
16. Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort, Journal of Allergy and Clinical Immunology: In Practice (2019)
17. Different Phenotypes of the Same Xiap Mutation in a Family: A Case of Xiap Deficiency With Juvenile Idiopathic Arthritis, Pediatric Blood and Cancer (2019)
18. Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis, Journal of Clinical Immunology (2018)
19. Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis, Journal of Clinical Immunology (2018)
20. The Effect of Intensive Phototherapy on Management of Hyperbilirubinemia in Neonates With the Gestational Age of 34 Weeks and More, Iranian Journal of Neonatology (2017)