19 results on '"Rasouli, Seyed Erfan"'
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2. The Autoimmune Manifestations in Patients with Genetic Defects in the B Cell Development and Differentiation Stages
3. Clinical heterogeneity in families with multiple cases of inborn errors of immunity
4. Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry
5. Diversity of malignancies in patients with different types of inborn errors of immunity
6. Pulmonary Complications of Monogenic Patients with Common Variable Immunodeficiency: COVID-19 Perspectives.
7. Autoimmune versus Non-autoimmune Cutaneous Features in Monogenic Patients with Inborn Errors of Immunity
8. Clinical Manifestation for Immunoglobulin A Deficiency: A Systematic Review and Metaanalysis
9. Additional file 1 of Diversity of malignancies in patients with different types of inborn errors of immunity
10. Cardiac Complications in Patients with Common Variable Immune Deficiency: A Longitudinal Study
11. Monogenic Disorder Associated with Autoimmune Lymphoproliferative Syndrome -Like Phenotype: A Systematic Review
12. Diversity of Malignancies in Patients with Different Types of Inborn Errors of Immunity
13. The Effects of Stimulation with PMA/Ionomycin on CD4+ T Cell Proliferation and Surface CD4 Molecule Modulation of Patients with LRBA Deficiency and CVID with the Unsolved Genetic Defect
14. Joint Involvement in Patients with LPS-Responsive and Beige-Like Anchor Protein (LRBA) Deficiency: A Case Report and Literature Review
15. The Origins of the First Reported Cases of the Primary Immunodeficiency Diseases
16. Monogenic Primary Immunodeficiency Disorder Associated with Common Variable Immunodeficiency and Autoimmunity
17. Autoimmune manifestations among 461 patients with monogenic inborn errors of immunity.
18. The Effects of G2013 (α-L-guluronic Acid) in a Pentylenetetrazole-induced Kindling Animal Model of Epilepsy.
19. The Effects of Stimulation with PMA/Ionomycin on CD4+ T Cell Proliferation and Surface CD4 Molecule Modulation of Patients with LRBA Deficiency and CVID with the Unsolved Genetic Defect.
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