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Two risk factors for hypozincemia in diabetic β-thalassemia patients: Hepatitis C and deferasirox

PloS one, 2024-01, Vol.19 (1), p.e0284267-e0284267

2024

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Ferritin thresholds for cardiac and liver hemosiderosis in β-thalassemia patients: a diagnostic accuracy study

Scientific reports, 2022-10, Vol.12 (1), p.17996-17996, Article 17996

2022

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Moderate to severe liver siderosis and raised AST are independent risk factors for vitamin D insufficiency in β-thalassemia patients

Scientific reports, 2020-12, Vol.10 (1), p.21164, Article 21164

2020

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The Effect of Resveratrol on Gamma Globin Gene Expression in Patients with Beta Thalassemia: The Role of Adaptation to Cellular Stress

Thalassemia reports, 2024-09, Vol.14 (3), p.71-80

2024

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Liver iron concentration is an independent risk factor for the prediabetic state in β-thalassemia patients

International journal of diabetes in developing countries, 2020-04, Vol.40 (2), p.227-234

2020

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Identification of β-globin haplotypes linked to sickle hemoglobin (Hb S) alleles in Mazandaran province, Iran

Genes & Genetic Systems, 2016/12/01, Vol.91(6), pp.311-313

2016

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Marriage and child bearing in patients with transfusion-dependent thalassemia major

The journal of obstetrics and gynaecology research, 2014-08, Vol.40 (8), p.1978-1982

2014

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Factors Related to Reduced Bone Density in β-Thalassemia Major Patients: Mazandaran Thalassemia Registry

Majallah-i dānishgāh-i ̕ulūm-i pizishkī va khadamāt-i bihdāshtī-darmānī Shahīd Ṣadūqī Yazd, 2023-09

2023

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Amlodipine Therapy in β-Thalassemia Patients: A Systematic Review and Meta-Analysis on Ferritin Levels and Liver MRI T2

Thalassemia reports, 2023-12, Vol.13 (4), p.241-252

2023

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Letter to Editor: Some Comments on "Effects of Zero- and 90-Degree Abduction of Glenohumeral Joint on the Upper Extremity Nerve Conduction Velocity (NCV) in Patients with Diabetes Undergoing Coronary Artery Bypass Graft Surgery"

Majallah-i dānishkadah-i pizishkī-i Iṣfahān. (Online), 2017-03, Vol.34 (413), p.1607-1609

2017

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β-Globin gene cluster haplotypes of Hb D-Los Angeles in Mazandaran Province, Iran

Genes & Genetic Systems, 2015/02/01, Vol.90(1), pp.55-57

2015

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Potential Effects of Silymarin and Its Flavonolignan Components in Patients with β-Thalassemia Major: A Comprehensive Review in 2015

Advances in Pharmacological Sciences, 2016-01, Vol.2016 (2016), p.1-8

2016

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Decrease of Hepatitis C Burden in Patients With Transfusion Dependent Beta Thalassemia Major, Thalassemia Research Center, 1995 – 2014

Journal of Pediatrics Review, 2015-07, Vol.3 (2), p.35-37

2015

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Prenatal diagnosis in Islamic countries: A narrative review in 2013

Journal of Pediatrics Review, 2014-02, Vol.2 (1), p.47-54

2014

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In Vitro Hb Production in Β-thalassemia Patients Is Not a Predictor of Clinical Responsiveness to Hydroxyurea

Iranian journal of public health, 2017-07, Vol.46 (7), p.948

2017

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Co-inheritance of --MED double gene deletion and αααAnti3.7 triplication on α-globin gene in Mazandaran at 2016

Research in molecular medicine, 2017-02, Vol.5 (1), p.44-47

2017

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Silymarin therapy and improvement of cardiac outcome in patients with β-thalassemia major

Journal of Research in Pharmacy Practice, 2016-01, Vol.5 (1), p.74-75

2016

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Combination Iron Chelation Therapy with Deferiprone and Deferasirox in Iron-Overloaded Patients with Transfusiondependent β-thalassemia Major

Clinics and practice, 2017-01, Vol.7 (1), p.912

2017

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Time to Do Something for Vitamin D Deficiency; A Review

Journal of Pediatrics Review, 2015-01, Vol.3 (1), p.1-6

2015

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Two risk factors for hypozincemia in diabetic [beta]-thalassemia patients: Hepatitis C and deferasirox

PloS one, 2024-01, Vol.19 (1), p.e0284267

2024

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Iron chelation and liver disease healing activity of edible mushroom (Cantharellus cibarius), in vitro and in vivo assays

RSC advances, 2015-01, Vol.5 (7), p.484-481

2015

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Letter to Editor

Journal of Pediatrics Review, 2014-07, Vol.2 (2), p.78-79

Mehrnoush Kosaryan

2014

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Co-existence of Phenylketonuria (PKU) and beta-Thalassemia Major in a 16 Years Old Girl: A Case Report

International journal of hematology- oncology and stem cell research, 2012-09, Vol.6 (3)

2012

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Non-invasive prenatal diagnosis of β-thalassemia by detection of the cell-free fetal DNA in maternal circulation: a systematic review and meta-analysis

Annals of hematology, 2016-08, Vol.95 (8), p.1341-1350

2016

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A double‐blind, controlled, crossover trial of amlodipine on iron overload status in transfusion dependent β‐thalassemia patients

International journal of clinical practice (Esher), 2021-08, Vol.75 (8), p.e14337-n/a

2021

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Two risk factors for hypozincemia in diabetic β-thalassemia patients: Hepatitis C and deferasirox

Ferritin thresholds for cardiac and liver hemosiderosis in β-thalassemia patients: a diagnostic accuracy study

Moderate to severe liver siderosis and raised AST are independent risk factors for vitamin D insufficiency in β-thalassemia patients

The Effect of Resveratrol on Gamma Globin Gene Expression in Patients with Beta Thalassemia: The Role of Adaptation to Cellular Stress

Liver iron concentration is an independent risk factor for the prediabetic state in β-thalassemia patients

Identification of β-globin haplotypes linked to sickle hemoglobin (Hb S) alleles in Mazandaran province, Iran

Marriage and child bearing in patients with transfusion-dependent thalassemia major

Factors Related to Reduced Bone Density in β-Thalassemia Major Patients: Mazandaran Thalassemia Registry

Amlodipine Therapy in β-Thalassemia Patients: A Systematic Review and Meta-Analysis on Ferritin Levels and Liver MRI T2

Letter to Editor: Some Comments on "Effects of Zero- and 90-Degree Abduction of Glenohumeral Joint on the Upper Extremity Nerve Conduction Velocity (NCV) in Patients with Diabetes Undergoing Coronary Artery Bypass Graft Surgery"

β-Globin gene cluster haplotypes of Hb D-Los Angeles in Mazandaran Province, Iran

Potential Effects of Silymarin and Its Flavonolignan Components in Patients with β-Thalassemia Major: A Comprehensive Review in 2015

Decrease of Hepatitis C Burden in Patients With Transfusion Dependent Beta Thalassemia Major, Thalassemia Research Center, 1995 – 2014

Prenatal diagnosis in Islamic countries: A narrative review in 2013

In Vitro Hb Production in Β-thalassemia Patients Is Not a Predictor of Clinical Responsiveness to Hydroxyurea

Co-inheritance of --MED double gene deletion and αααAnti3.7 triplication on α-globin gene in Mazandaran at 2016

Silymarin therapy and improvement of cardiac outcome in patients with β-thalassemia major

Combination Iron Chelation Therapy with Deferiprone and Deferasirox in Iron-Overloaded Patients with Transfusiondependent β-thalassemia Major

Time to Do Something for Vitamin D Deficiency; A Review

Two risk factors for hypozincemia in diabetic [beta]-thalassemia patients: Hepatitis C and deferasirox

Iron chelation and liver disease healing activity of edible mushroom (Cantharellus cibarius), in vitro and in vivo assays

Letter to Editor

Co-existence of Phenylketonuria (PKU) and beta-Thalassemia Major in a 16 Years Old Girl: A Case Report

Non-invasive prenatal diagnosis of β-thalassemia by detection of the cell-free fetal DNA in maternal circulation: a systematic review and meta-analysis

A double‐blind, controlled, crossover trial of amlodipine on iron overload status in transfusion dependent β‐thalassemia patients

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