Thrombophilic gene polymorphisms are associated with deep venous thrombosis in a cohort of Egyptian patients

HH Essa, H Gobran, SM Sabry… - The Egyptian Journal of …, 2019 - journals.lww.com
Background There is several evidence suggesting, that inherited thrombophilia increases
the susceptibility to venous thromboembolism (VTE). Aim is to detect prothrombotic genes …

[HTML][HTML] Polymorphisms in thrombophilic genes are associated with deep venous thromboembolism in an Iranian population

M Farajzadeh, N Bargahi, AP Zonouzi, D Farajzadeh… - Meta gene, 2014 - Elsevier
It has been revealed that the inherited thrombophilia increases the risk of thrombosis in the
venous system. To study the association of factor V G1691A, factor V HR2 (4070A/G) …

Study of thrombophilic gene polymorphisms in Egyptian patients with deep venous thrombosis using in situ hybridization technique.

NI Azab, RF Salim, MS Darwish - Bulletin of Egyptian Society …, 2017 - besps.journals.ekb.eg
Up to 70% of thrombotic patients with no identifiable risk factors were termed idiopathic.
Now, molecular diagnostics combined with existing laboratory techniques allow accurate …

Frequency of thrombophilia gene polymorphisms: factor V Leiden, prothrombin G20210A, methylenetetrahydrofolate-reductase and platelet PLA2 antigen in …

B Pourgheysari, E Farrokhi… - Feyz Journal of Kashan …, 2012 - search.ebscohost.com
Background: Inherited thrombophilic gene polymorphisms have been related to the
pathogenesis of venous thromboembolism and its outcomes. Considering the scarcity of …

Genetic risk factors in patients with deep venous thrombosis, a retrospective case control study on Iranian population

S Hosseini, E Kalantar, MS Hosseini, S Tabibian… - Thrombosis journal, 2015 - Springer
Background Venous thromboembolism (VTE) could be manifested as deep venous
thrombosis (DVT) or pulmonary embolism (PE). DVT is usually the more common …

The contributions of thrombophilic mutations to genetic susceptibility to deep venous thrombosis in iraqi patients

NAS Al-Allawi, AIA Badi, MA Goran… - Genetic Testing and …, 2015 - liebertpub.com
Background and Aims: There is a paucity of data on the contribution of various thrombophilic
mutations to the development of venous thrombosis in Iraqi patients. Therefore we designed …

[HTML][HTML] Molecular Analysis Of Patients With Deep Venous Thrombosis

S Hosseeini, E Kalantari, A Dorgalaleh, A Rozei… - Blood, 2013 - Elsevier
Background Deep venous thrombosis (DVT) refers to the formation of a thrombus within a
deep vein that frequently occurs after surgical procedures, trauma, in the presence of cancer …

A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous …

WY Almawi, H Tamim, R Kreidy, G Timson… - Journal of thrombosis …, 2005 - Springer
Background: Insofar as the inherited prothrombotic single nucleotide polymorphisms (SNPs)
factor V G1691A (FV-Leiden), prothrombin (PRT) G20210A, and methylenetetrahydrofolate …

[HTML][HTML] Association of Homozygous Thrombophilia Polymorphisms and Venous Thromboembolism in Shahrekord, Iran

H Rouhi-Broujeni, B Pourgheysari, AM Hasheminia - Tanaffos, 2016 - ncbi.nlm.nih.gov
Background: Venous thromboembolism (VTE) is a major cause of mortality. Factor V Leiden
(FVL), methylenetetrahydrofolate reductase (MTHFR) C677T, and prothrombin (FII) …

Deep venous thrombosis and thrombophilic mutations in western Iran: association with factor V Leiden

Z Rahimi, H Mozafari, A Shahriari-Ahmadi… - Blood coagulation & …, 2010 - journals.lww.com
The aim of present study was to investigate the prevalence of factor V Leiden (FVL) c.
1691G> A, prothrombin g. 20210G> A and methylenetetrahydrofolate reductase (MTHFR) c …