Study of alloimmunization and autoimmunization in Iranian β-thalassemia major patients

Por Davari, Kambiz, Soltanpour, Mohammad Soleiman
Publicado no Asian J Transfus Sci (2016)

The Correlation of Cardiac and Hepatic Hemosiderosis as Measured by T2*MRI Technique with Ferritin Levels and Hemochromatosis Gene Mutations in Iranian Patients with Beta Thalassem...

Por Soltanpour, Mohammad Soleiman, Davari, Kambiz
Publicado no Oman Med J (2018)

Assessment of the role of plasma nitric oxide levels, T-786C genetic polymorphism, and gene expression levels of endothelial nitric oxide synthase in the development of coronary ar...

Por Mahmoodi, Khalil, Soltanpour, Mohammad Soleiman, Kamali, Koorosh
Publicado no J Res Med Sci (2017)

Association Study of the ATP - Binding Cassette Transporter A1 (ABCA1) Rs2230806 Genetic Variation with Lipid Profile and Coronary Artery Disease Risk in an Iranian Population

Por Ghaznavi, Habib, Aali, Ehsan, Soltanpour, Mohammad Soleiman
Publicado no Open Access Maced J Med Sci (2018)

A preliminary study of the association between the ABCA1 gene promoter DNA methylation and coronary artery disease risk

Por Ghaznavi, Habib, Mahmoodi, Khalil, Soltanpour, Mohammad Soleiman
Publicado no Mol Biol Res Commun (2018)

Association study of methylenetetrahydrofolate reductase A1298C mutation with cerebral venous thrombosis risk in an Iranian population

Por Habib, Ghaznavi, Zahra, Soheili, Shahram, Samiei, Soltanpour, Mohammad Soleiman
Publicado no Int J Appl Basic Med Res (2015)

Association of Methylenetetrahydrofolate Reductase C677T Polymorphism with Hyperhomocysteinemia and Deep Vein Thrombosis in the Iranian Population

Por Ghaznavi, Habib, Soheili, Zahra, Samiei, Shahram, Soltanpour, Mohammad Soleiman
Publicado no Vasc Specialist Int (2015)

Role of Hyperhomocysteinemia and Methylene Tetrahydrofolate Reductase C677T Polymorphism in Idiopathic Portal Vein Thrombosis

Por Ghaznavi, Habib, Soheili, Zahra, Samiei, Shahram, Soltanpour, Mohammad Soleiman
Publicado no Vasc Specialist Int (2016)

Association of Nitric Oxide Levels and Endothelial Nitric Oxide Synthase G894T Polymorphism with Coronary Artery Disease in the Iranian Population

Por Mahmoodi, Khalil, Nasehi, Leila, Karami, Elham, Soltanpour, Mohammad Soleiman
Publicado no Vasc Specialist Int (2016)

Plasma concentration, genetic variation, and gene expression levels of matrix metalloproteinase 9 in Iranian patients with coronary artery disease

Por Mahmoodi, Khalil, Kamali, Koorosh, Karami, Elham, Soltanpour, Mohammad Soleiman
Publicado no J Res Med Sci (2017)

The C-565T Polymorphism (rs2422493) of the ATP-binding Cassette Transporter A1 Gene Contributes to the Development and Severity of Coronary Artery Disease in an Iranian Population

Por Mahmoodi, Khalil, Kamali, Koorosh, Ghaznavi, Habib, Soltanpour, Mohammad Soleiman
Publicado no Oman Med J (2018)

Evaluation of the Role of -137G/C Single Nucleotide Polymorphism (rs187238) and Gene Expression Levels of the IL-18 in Patients with Coronary Artery Disease

Por Hoseini, Fatemeh, Mahmazi, Sanaz, Mahmoodi, Khalil, Jafari, Gholam Ali, Soltanpour, Mohammad Soleiman
Publicado no Oman Med J (2018)

Methylenetetrahydrofolate reductase C677T mutation and risk of retinal vein thrombosis

Por Soltanpour, Mohammad Soleiman, Soheili, Zahra, Shakerizadeh, Ali, Pourfathollah, Ali Akbar, Samiei, Shahram, Meshkani, Reza, Shahjahani, Mohammad, Karimi, Abbas
Publicado em 2013