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Aberrant peripheral blood CD4+ CD25+ FOXP3+ regulatory T cells/T helper-17 number is associated with the outcome of patients with lymphoma

Cancer Immunology, Immunotherapy, 2020-09, Vol.69 (9), p.1917-1928

2020

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Immune Microenvironment in Hematologic Malignancies

Iranian journal of medical sciences, 2023-01, Vol.48 (1), p.1-3

2023

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The impact of selenium on regulatory T cell frequency and immune checkpoint receptor expression in patients with diffuse large B cell lymphoma (DLBCL)

Cancer Immunology, Immunotherapy, 2021-10, Vol.70 (10), p.2961-2969

2021

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Atopy manifestations in pediatric patients with acute lymphoblastic leukemia: correlation assessment with interleukin-4 (IL-4) and IgE level

BMC pediatrics, 2022-03, Vol.22 (1), p.149-149, Article 149

2022

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Expression of the immune checkpoint receptors CTLA-4, LAG-3, and TIM-3 in β-thalassemia major patients: correlation with alloantibody production and regulatory T cells (Tregs) phenotype

Annals of hematology, 2021-10, Vol.100 (10), p.2463-2469

2021

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Overexpression of indoleamine 2,3-dioxygenase correlates with regulatory T cell phenotype in acute myeloid leukemia patients with normal karyotype

Blood Research, 2018, 53(4), , pp.294-298

2018

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Abnormal frequency of the memory B cell subsets and plasmablasts in patients with congenital severe hemophilia A: correlation with “Inhibitor” formation

Blood Research, 2024, 59(2), , pp.16-16

2024

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FMS-Like Tyrosine Kinase 3 (FLT3) and Nucleophosmin 1 (NPM1) in Iranian Adult Acute Myeloid Leukemia Patients with Normal Karyotypes: Mutation Status and Clinical and Laboratory Characteristics

Turkish journal of haematology, 2017-12, Vol.34 (4), p.300-306

2017

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Association Between Cytotoxic T-Lymphocyte Antigen 4 Gene Polymorphisms and Torque Teno Virus Infection After Hematopoietic Stem Cell Transplantation

Experimental and clinical transplantation, 2021-03, Vol.19 (3), p.259-263

2021

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Genetic Variation of Costimulatory Molecules, Including Cytotoxic T-Lymphocyte Antigen 4, Inducible T-Cell Costimulator, Cluster Differentiation 28, and Programmed Cell Death 1 Genes, in Iranian Patients With Leukemia

Experimental and clinical transplantation, 2020-11, Vol.18 (6), p.719-724

2020

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Alteration in frequency and function of CD4⁺CD25⁺FOXP3⁺ regulatory T cells in patients with immune thrombocytopenic purpura

Iranian journal of allergy, asthma, and immunology, 2014-04, Vol.13 (2), p.85-92

2014

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Polymorphism in Exon 2 of CD1 Genes in Southwest of Iran

Iranian journal of public health, 2013-07, Vol.42 (7), p.775-782

2013

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Higher Peripheral Blood IFN-γ-/IL-4+ Th2 Lymphocytes Are Associated with Lower Rate of Relapse in Patients with Lymphoma

Immunological investigations, 2022-02, Vol.51 (2), p.452-463

2022

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Altered frequency of FOXP3 + regulatory T cells is associated with development of inhibitors in patients with severe hemophilia A

International journal of laboratory hematology, 2023-12, Vol.45 (6), p.953-960

2023

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Selenium Supplementation Alter the Frequency of Th17 but not Th1/Th2 Lymphocytes in Diffuse Large B Cell Lymphoma Patients

Clinical laboratory (Heidelberg), 2023-01, Vol.69 (1)

2023

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The prognostic significance of immune checkpoint receptor expression in patients with lymphoma: Association with disease status and clinical outcomes

Asia-Pacific journal of clinical oncology, 2022-10, Vol.18 (5), p.e388-e397

2022

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Correction: Abnormal frequency of the memory B cell subsets and plasmablasts in patients with congenital severe hemophilia A: correlation with “Inhibitor” formation

Blood research, 2024-04, Vol.59 (1), p.17-17, Article 17

2024

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Association of killer‐cell immunoglobulin‐like receptor genes with acute myelogenous leukaemia

International journal of immunogenetics, 2020-12, Vol.47 (6), p.512-521

2020

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Study of the Serum Immunoglobulin and Cell-Mediated Immunity in Patients with Congenital Severe Hemophilia

Clinical laboratory (Heidelberg), 2021-08, Vol.67 (8/2021)

2021

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Evaluation of CD4+CD25+FOXP3+ regulatory T cells function in patients with common variable immunodeficiency

Cellular immunology, 2013-02, Vol.281 (2), p.129-133

2013

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Aberrant Expression of the miR-181b/miR-222 after Hematopoietic Stem Cell Transplantation in Patients with Acute Myeloid Leukemia

Indian journal of hematology & blood transfusion, 2019-07, Vol.35 (3), p.446-450

2019

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Mutation of the DNMT3A and IDH1/2 genes in Iranian acute myeloid leukemia patients with normal karyotype (CN-AML): association with other gene mutation and clinical and laboratory characteristics

Journal of hematopathology, 2018-06, Vol.11 (2), p.29-36

2018

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Efficacy of Deferasirox (Exjade®) in Modulation of Iron Overload in Patients with β-Thalassemia Intermedia

Hemoglobin, 2015-09, Vol.39 (5), p.327-329

2015

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FMS-like Tyrosine Kinase 3 (FLT3) and Nucleophosmin 1 (NPM1) in Iranian Adult Acute Myeloid Leukemia (AML) Patients with Normal Karyotype; Mutation Status and Clinical and Laboratory Characteristics

Turkish journal of haematology, 2017-03

2017

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Polymorphism in Exon 2 of CD1 Genes in Southwest of Iran

Iranian journal of public health, 2013-07, Vol.42 (7)

2013

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Aberrant peripheral blood CD4+ CD25+ FOXP3+ regulatory T cells/T helper-17 number is associated with the outcome of patients with lymphoma

Immune Microenvironment in Hematologic Malignancies

The impact of selenium on regulatory T cell frequency and immune checkpoint receptor expression in patients with diffuse large B cell lymphoma (DLBCL)

Atopy manifestations in pediatric patients with acute lymphoblastic leukemia: correlation assessment with interleukin-4 (IL-4) and IgE level

Expression of the immune checkpoint receptors CTLA-4, LAG-3, and TIM-3 in β-thalassemia major patients: correlation with alloantibody production and regulatory T cells (Tregs) phenotype

Overexpression of indoleamine 2,3-dioxygenase correlates with regulatory T cell phenotype in acute myeloid leukemia patients with normal karyotype

Abnormal frequency of the memory B cell subsets and plasmablasts in patients with congenital severe hemophilia A: correlation with “Inhibitor” formation

FMS-Like Tyrosine Kinase 3 (FLT3) and Nucleophosmin 1 (NPM1) in Iranian Adult Acute Myeloid Leukemia Patients with Normal Karyotypes: Mutation Status and Clinical and Laboratory Characteristics

Association Between Cytotoxic T-Lymphocyte Antigen 4 Gene Polymorphisms and Torque Teno Virus Infection After Hematopoietic Stem Cell Transplantation

Genetic Variation of Costimulatory Molecules, Including Cytotoxic T-Lymphocyte Antigen 4, Inducible T-Cell Costimulator, Cluster Differentiation 28, and Programmed Cell Death 1 Genes, in Iranian Patients With Leukemia

Alteration in frequency and function of CD4⁺CD25⁺FOXP3⁺ regulatory T cells in patients with immune thrombocytopenic purpura

Polymorphism in Exon 2 of CD1 Genes in Southwest of Iran

Higher Peripheral Blood IFN-γ-/IL-4+ Th2 Lymphocytes Are Associated with Lower Rate of Relapse in Patients with Lymphoma

Altered frequency of FOXP3 + regulatory T cells is associated with development of inhibitors in patients with severe hemophilia A

Selenium Supplementation Alter the Frequency of Th17 but not Th1/Th2 Lymphocytes in Diffuse Large B Cell Lymphoma Patients

The prognostic significance of immune checkpoint receptor expression in patients with lymphoma: Association with disease status and clinical outcomes

Correction: Abnormal frequency of the memory B cell subsets and plasmablasts in patients with congenital severe hemophilia A: correlation with “Inhibitor” formation

Association of killer‐cell immunoglobulin‐like receptor genes with acute myelogenous leukaemia

Study of the Serum Immunoglobulin and Cell-Mediated Immunity in Patients with Congenital Severe Hemophilia

Evaluation of CD4+CD25+FOXP3+ regulatory T cells function in patients with common variable immunodeficiency

Aberrant Expression of the miR-181b/miR-222 after Hematopoietic Stem Cell Transplantation in Patients with Acute Myeloid Leukemia

Mutation of the DNMT3A and IDH1/2 genes in Iranian acute myeloid leukemia patients with normal karyotype (CN-AML): association with other gene mutation and clinical and laboratory characteristics

Efficacy of Deferasirox (Exjade®) in Modulation of Iron Overload in Patients with β-Thalassemia Intermedia

FMS-like Tyrosine Kinase 3 (FLT3) and Nucleophosmin 1 (NPM1) in Iranian Adult Acute Myeloid Leukemia (AML) Patients with Normal Karyotype; Mutation Status and Clinical and Laboratory Characteristics

Polymorphism in Exon 2 of CD1 Genes in Southwest of Iran

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