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‘Harlequin cells’ in lymphocyte‐variant hypereosinophilia

EJHaem, 2022-11, Vol.3 (4), p.1390-1391

2022

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Correction to: Mixed-phenotype acute leukemia characteristics: first report from Iran

Clinical and experimental medicine, 2021-05, Vol.21 (2), p.341-341

2021

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Prognostic correlation of NOTCH1 and SF3B1 mutations with chromosomal abnormalities in chronic lymphocytic leukemia patients

Cancer reports, 2023-03, Vol.6 (3), p.e1757-n/a

2023

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Paroxysmal nocturnal haemoglobinuria, diagnosis and haematological findings, first report from Iran, model for developing countries

EJHaem, 2022-05, Vol.3 (2), p.335-340

2022

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Mixed-phenotype acute leukemia characteristics: first report from Iran

Clinical and experimental medicine, 2018-11, Vol.18 (4), p.513-521

2018

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Detection of Human Metapneumovirus and Respiratory Syncytial Virus by Real-Time Polymerase Chain Reaction Among Hospitalized Young Children in Iran

Jundishapur journal of microbiology, 2016-03, Vol.9 (3), p.e32974-e32974

2016

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Platelets in the perspective of COVID-19; pathophysiology of thrombocytopenia and its implication as prognostic and therapeutic opportunity

International immunopharmacology, 2021-10, Vol.99, p.107995-107995, Article 107995

2021

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Enzyme Polymorphism in Warfarin Dose Management After Pediatric Cardiac Surgery

Research in cardiovascular medicine, 2015-08, Vol.4 (3), p.e27963-e27963

2015

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Genetic Polymorphisms of CYP2C19 and Resistance to Clopidogrel Therapy among Iranian Patients Suffering from Ischemic Heart Disease

Research in molecular medicine, 2016-07, Vol.4 (3), p.41-46

2016

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Combination of minimal residual disease on day 15 and copy number alterations results in BCR-ABL1-negative pediatric B-ALL: A powerful tool for prediction of induction failure

Cancer genetics, 2024-04, Vol.282-283, p.27-34

2024

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Dihydrorhodamine-123 flow cytometry method: time for substantial revision in technical procedure

Laboratory medicine, 2024-09

2024

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Altering chromatin methylation patterns and the transcriptional network involved in regulation of hematopoietic stem cell fate

Journal of cellular physiology, 2020-10, Vol.235 (10), p.6404-6423

2020

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The incidence of TP53 mutations in patients with chronic lymphocytic leukemia in Iran

Asian journal of oncology, 2024-06, Vol.10, p.2, Article 2

2024

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The proportion of different BCR-ABL1 transcript types in chronic myeloid leukemia. An international overview

Leukemia, 2019-05, Vol.33 (5), p.1173-1183

2019

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Distinct power of bone marrow microRNA signatures and tumor suppressor genes for early detection of acute leukemia

Clinical & translational oncology, 2022-07, Vol.24 (7), p.1372-1380

2022

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Integrating rapamycin with novel PI3K/Akt/mTOR inhibitor microRNAs on NOTCH1-driven T-cell acute lymphoblastic leukemia (T-ALL)

Bioimpacts, 2024-01, Vol.14 (4), p.1-12

2024

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ABL Kinase Domain Mutations in Iranian Chronic Myeloid Leukemia Patients with Resistance to Tyrosine Kinase Inhibitors

Laboratory medicine, 2021-03, Vol.52 (2), p.158-167

2021

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Evaluation of BRAF-V600E gene mutation in colon tissue of patients with colorectal cancer in Iran

Majallah-i ̒ulum-i pizishkī, 2022-09, Vol.32 (3), p.303-310

2022

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Thrombophilic Mutations in Iranian Patients With Thrombophilia

Laboratory medicine, 2013-02, Vol.44 (1), p.e62-e68

2013

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A Cross-Sectional Study for Evaluation of KRAS and BRAF Mutations by Reverse Dot Blot, PCR-RFLP, and Allele-Specific PCR Methods Among Patients with Colorectal Cancer

Avicenna journal of medical biotechnology, 2021-10, Vol.13 (4), p.183-191

2021

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The Effect of Demographic Factors and VKORC1 1639 G>A Genotypes on Estimated Warfarin Maintenance Dose in Iranian Patients Under Warfarin Therapy

Indian journal of hematology & blood transfusion, 2019-01, Vol.35 (1), p.167-171

2019

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A Six-Month Survey of the Frequency of Extensively Drug-resistant Gram-Negative Bacteria by VITEK 2 System in 2020

Majallah-i mīkrub/shināsī-i pizishkī-i Īrān, 2022-02, Vol.16 (2), p.134-140

2022

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Adoptive Treg cell-based immunotherapy: Frontier therapeutic aspects in rheumatoid arthritis

Immunotherapy, 2020-08, Vol.12 (12), p.933-946

2020

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Polymorphism and synergism of angiotensin-converting enzyme (ACE) and plasminogen activator inhibitor-1 (PAI-1) genes in coronary artery disease

Journal of the renin-angiotensin-aldosterone system, 2015-12, Vol.16 (4), p.1168-1174

2015

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In Ph+BCR-ABL1P210+ acute lymphoblastic leukemia the e13a2 (B2A2) transcript is prevalent

Leukemia, 2020-03, Vol.34 (3), p.929-931

2020

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‘Harlequin cells’ in lymphocyte‐variant hypereosinophilia

Correction to: Mixed-phenotype acute leukemia characteristics: first report from Iran

Prognostic correlation of NOTCH1 and SF3B1 mutations with chromosomal abnormalities in chronic lymphocytic leukemia patients

Paroxysmal nocturnal haemoglobinuria, diagnosis and haematological findings, first report from Iran, model for developing countries

Mixed-phenotype acute leukemia characteristics: first report from Iran

Detection of Human Metapneumovirus and Respiratory Syncytial Virus by Real-Time Polymerase Chain Reaction Among Hospitalized Young Children in Iran

Platelets in the perspective of COVID-19; pathophysiology of thrombocytopenia and its implication as prognostic and therapeutic opportunity

Enzyme Polymorphism in Warfarin Dose Management After Pediatric Cardiac Surgery

Genetic Polymorphisms of CYP2C19 and Resistance to Clopidogrel Therapy among Iranian Patients Suffering from Ischemic Heart Disease

Combination of minimal residual disease on day 15 and copy number alterations results in BCR-ABL1-negative pediatric B-ALL: A powerful tool for prediction of induction failure

Dihydrorhodamine-123 flow cytometry method: time for substantial revision in technical procedure

Altering chromatin methylation patterns and the transcriptional network involved in regulation of hematopoietic stem cell fate

The incidence of TP53 mutations in patients with chronic lymphocytic leukemia in Iran

The proportion of different BCR-ABL1 transcript types in chronic myeloid leukemia. An international overview

Distinct power of bone marrow microRNA signatures and tumor suppressor genes for early detection of acute leukemia

Integrating rapamycin with novel PI3K/Akt/mTOR inhibitor microRNAs on NOTCH1-driven T-cell acute lymphoblastic leukemia (T-ALL)

ABL Kinase Domain Mutations in Iranian Chronic Myeloid Leukemia Patients with Resistance to Tyrosine Kinase Inhibitors

Evaluation of BRAF-V600E gene mutation in colon tissue of patients with colorectal cancer in Iran

Thrombophilic Mutations in Iranian Patients With Thrombophilia

A Cross-Sectional Study for Evaluation of KRAS and BRAF Mutations by Reverse Dot Blot, PCR-RFLP, and Allele-Specific PCR Methods Among Patients with Colorectal Cancer

The Effect of Demographic Factors and VKORC1 1639 G>A Genotypes on Estimated Warfarin Maintenance Dose in Iranian Patients Under Warfarin Therapy

A Six-Month Survey of the Frequency of Extensively Drug-resistant Gram-Negative Bacteria by VITEK 2 System in 2020

Adoptive Treg cell-based immunotherapy: Frontier therapeutic aspects in rheumatoid arthritis

Polymorphism and synergism of angiotensin-converting enzyme (ACE) and plasminogen activator inhibitor-1 (PAI-1) genes in coronary artery disease

In Ph+BCR-ABL1P210+ acute lymphoblastic leukemia the e13a2 (B2A2) transcript is prevalent

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