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The First Case of BENTA Disease (B Cell Expansion with NF-κB and T Cell Anergy) from Iran

Journal of clinical immunology, 2021-05, Vol.41 (4), p.811-813

2021

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Hepcidin gene polymorphisms and iron overload in β-thalassemia major patients refractory to iron chelating therapy

BMC medical genetics, 2020-04, Vol.21 (1), p.75-75, Article 75

2020

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miR-30a regulates γ-globin expression in erythoid precursors of intermedia thalassemia through targeting BCL11A

Molecular biology reports, 2020-05, Vol.47 (5), p.3909-3918

2020

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Novel mutations in mitochondrial carrier family gene SLC25A38, causing congenital sideroblastic anemia in Iranian families, identified by whole exome sequencing

Blood cells, molecules, & diseases, 2018-07, Vol.71, p.39-44

2018

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Coronavirus Disease 2019 (COVID-19) Severity in Patients with Thalassemias: A Nationwide Iranian Experience

Mediterranean journal of hematology and infectious diseases, 2021, Vol.13 (1), p.e2021008-e2021008

2021

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Resistance-associated substitutions (RASs) to HCV direct-acting antivirals (DAAs) at baseline of treatment in thalassemia patients: a referral center study

Archives of virology, 2020-10, Vol.165 (10), p.2193-2203

2020

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Kidd Blood Group Genotyping for Thalassemia Patient in Iran

Indian journal of hematology & blood transfusion, 2020-07, Vol.36 (3), p.550-555

2020

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Hydroxyurea responsiveness in β-thalassemic patients is determined by the stress response adaptation of erythroid progenitors and their differentiation propensity

Haematologica (Roma), 2013-05, Vol.98 (5), p.696-704

2013

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Complications in patients with transfusion dependent thalassemia: A descriptive cross‐sectional study

Health science reports, 2023-10, Vol.6 (10), p.e1624-n/a

2023

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Effect of quercetin on oxidative stress and liver function in beta-thalassemia major patients receiving desferrioxamine: A double-blind randomized clinical trial

Journal of research in medical sciences, 2019-01, Vol.24 (1), p.91-91

2019

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Red Blood Cell Immunization and Contributing Factors in 685 Thalassemia Patients

International journal of hematology- oncology and stem cell research, 2022, Vol.16 (1), p.9-14

2022

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Blood group genotyping in alloimmunized multi‐transfused thalassemia patients from Iran

Molecular genetics & genomic medicine, 2021-07, Vol.9 (7), p.e1701-n/a

2021

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A Large Cohort Study of Genotype and Phenotype Correlations of Beta- Thalassemia in Iranian Population

International journal of hematology- oncology and stem cell research, 2015-10, Vol.9 (4), p.198-202

2015

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Comparison of iron chelation effects of deferoxamine, deferasirox, and combination of deferoxamine and deferiprone on liver and cardiac T2 MRI in thalassemia maior

Caspian journal of internal medicine, 2017-01, Vol.8 (3), p.159-164

2017

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Comparative Evaluation of Biochemical and Hematological Parameters of Pre-Storage Leukoreduction during RBC Storage

International journal of hematology- oncology and stem cell research, 2018-01, Vol.12 (1), p.35-42

2018

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Inhibitory role of cAMP on doxorubicin-induced apoptosis in pre-B ALL cells through dephosphorylation of p53 serine residues

Apoptosis (London), 2010-02, Vol.15 (2), p.196-203

2010

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T2＊ magnetic resonance imaging of the liver in thalassemic patients in Iran

World journal of gastroenterology : WJG, 2011-01, Vol.17 (4), p.522-525

2011

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Renal Hemosiderosis among Iranian Transfusion Dependent β-Thalassemia Major Patients

International journal of hematology- oncology and stem cell research, 2017-04, Vol.11 (2), p.133-138

2017

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Novel variants in Iranian individuals suspected to have inherited red blood cell disorders, including bone marrow failure syndromes

Haematologica (Roma), 2020-01, Vol.105 (1), p.e1-e4

2020

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Major histocompatibility complex (MHC) antigens polymorphism and alloimmunization study in thalassemia patients with febrile non-hemolytic transfusion reaction (FNHTR)

Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine, 2023-05, Vol.30 (2), p.205-211

2023

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Prevalence and mortality in β‐thalassaemias due to outbreak of novel coronavirus disease (COVID‐19): the nationwide Iranian experience

British journal of haematology, 2020-08, Vol.190 (3), p.e137-e140

2020

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Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders

Transfusion and apheresis science, 2021-12, Vol.60 (6), p.103203-103203, Article 103203

2021

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JAK2V617F Allele Burden Measurement in Peripheral Blood of Iranian Patients with Myeloproliferative Neoplasms and Effect of Hydroxyurea on JAK2V617F Allele Burden

International journal of hematology- oncology and stem cell research, 2016-04, Vol.10 (2), p.70-78

2016

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The First Case of BENTA Disease (B Cell Expansion with NF-κB and T Cell Anergy) from Iran

Hepcidin gene polymorphisms and iron overload in β-thalassemia major patients refractory to iron chelating therapy

miR-30a regulates γ-globin expression in erythoid precursors of intermedia thalassemia through targeting BCL11A

Novel mutations in mitochondrial carrier family gene SLC25A38, causing congenital sideroblastic anemia in Iranian families, identified by whole exome sequencing

Coronavirus Disease 2019 (COVID-19) Severity in Patients with Thalassemias: A Nationwide Iranian Experience

Resistance-associated substitutions (RASs) to HCV direct-acting antivirals (DAAs) at baseline of treatment in thalassemia patients: a referral center study

Kidd Blood Group Genotyping for Thalassemia Patient in Iran

Evaluation of endocrine complications in beta-thalassemia intermedia (β-TI): a cross-sectional multicenter study

Hydroxyurea responsiveness in β-thalassemic patients is determined by the stress response adaptation of erythroid progenitors and their differentiation propensity

Complications in patients with transfusion dependent thalassemia: A descriptive cross‐sectional study

Effect of quercetin on oxidative stress and liver function in beta-thalassemia major patients receiving desferrioxamine: A double-blind randomized clinical trial

Red Blood Cell Immunization and Contributing Factors in 685 Thalassemia Patients

Blood group genotyping in alloimmunized multi‐transfused thalassemia patients from Iran

A Large Cohort Study of Genotype and Phenotype Correlations of Beta- Thalassemia in Iranian Population

Comparison of iron chelation effects of deferoxamine, deferasirox, and combination of deferoxamine and deferiprone on liver and cardiac T2 MRI in thalassemia maior

P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders

Comparative Evaluation of Biochemical and Hematological Parameters of Pre-Storage Leukoreduction during RBC Storage

Inhibitory role of cAMP on doxorubicin-induced apoptosis in pre-B ALL cells through dephosphorylation of p53 serine residues

T2＊ magnetic resonance imaging of the liver in thalassemic patients in Iran

Renal Hemosiderosis among Iranian Transfusion Dependent β-Thalassemia Major Patients

Novel variants in Iranian individuals suspected to have inherited red blood cell disorders, including bone marrow failure syndromes

Major histocompatibility complex (MHC) antigens polymorphism and alloimmunization study in thalassemia patients with febrile non-hemolytic transfusion reaction (FNHTR)

Prevalence and mortality in β‐thalassaemias due to outbreak of novel coronavirus disease (COVID‐19): the nationwide Iranian experience

Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders

JAK2V617F Allele Burden Measurement in Peripheral Blood of Iranian Patients with Myeloproliferative Neoplasms and Effect of Hydroxyurea on JAK2V617F Allele Burden

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