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Human Immunology|November 11, 2019
Exosomes derived from mesenchymal stem cells improved function and survival of neutrophils from severe congenital neutropenia patients in vitroMohammad Mahmoudi, Mahsa Taghavi-Farahabadi, Saeed Namaki, et al.Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|June 9, 2023
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype of a patientNegar Moradian, Samaneh Zoghi, Elham Rayzan, et al.Iranian Journal of Allergy, Asthma, and Immunology|July 13, 2022
The Clinical and Molecular Assessment of Iranian Families with Severe Congenital Neutropenia, Identification of HYOU1 and SHOC2 as Potential Novel Gene DefectsFatemeh Arab, Nima Rezaei, Forough Taheri, et al.Journal of Medical Case Reports|July 17, 2023
A novel X-linked mutation in IL2RG associated with early-onset inflammatory bowel disease: a case report of twin brothersElham Rayzan, Mona Sadeghalvad, Sepideh Shahkarami, et al.Human Immunology|September 6, 2020
Improving the function of neutrophils from chronic granulomatous disease patients using mesenchymal stem cells' exosomesMahsa Taghavi-Farahabadi, Mohammad Mahmoudi, Seyed Alireza Mahdaviani, et al.Endocrine, Metabolic & Immune Disorders Drug Targets|February 2, 2022
A 3-Year-Old Boy with an Xp21 Deletion Syndrome: A Case ReportShaghayegh Sadeghmousavi, Sepideh Shahkarami, Elham Rayzan, et al.Case Reports in Medicine|May 8, 2023
DNAH11 and a Novel Genetic Variant Associated with Situs Inversus: A Case Report and Review of the LiteratureFatemeh Sodeifian, Noosha Samieefar, Sepideh Shahkarami, et al.Allergologia Et Immunopathologia|February 28, 2021
Novel BTK mutation in X-linked agammaglobulinemia: Report of a 17-year-old maleZoha Shaka, Helia Mojtabavi, Elham Rayzan, et al.Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|December 26, 2023
Whole-exome sequencing to identify undiagnosed primary immunodeficiency disorders in children with community-acquired sepsis, admitted in the pediatric intensive care unitElham Rayzan, Mona Mirbeyk, Parmida Sadat Pezeshki, et al.Endocrine, Metabolic & Immune Disorders Drug Targets|April 8, 2022
Case Report of a Novel NFkB Mutation in a Lymphoproliferative Disorder PatientKhashayar Danandeh, Parnian Jabbari, Elham Rayzan, et al.Pageof 3