Prevalence and Multiplicity of Thrombophilia Genetic Polymorphisms of FV, MTHFR, FII, and PAI-I: A Cross-Sectional Study on a Healthy Jordanian Population

N Al-Zoubi, N Alrabadi, K Kheirallah… - International Journal of …, 2021 - Taylor & Francis
Background FV, MTHFR, II, and PAI-I are the most common genes associated with
thrombophilia genetic variants, which vary among different populations and ethnic groups …

Comparison between thrombophilic gene polymorphisms among high risk patients

M Levkova, M Hachmeriyan, M Stoyanova… - Romanian Journal of …, 2020 - sciendo.com
Methods. 200 patients, including 76 with thrombotic accidents and 124 with two or more
idiopathic recurrent miscarriage during the first trimester, were tested for the presence of …

Prevalence of thrombophilic gene polymorphisms in an Azari population of Iran

N Bargahi, M Farajzadeh, A Poursadegh-Zonouzi… - Hematology …, 2014 - mdpi.com
There is several evidence suggests that thrombophilic gene polymorphisms may influence
susceptibility to thromboembolic events. The prevalence of these polymorphisms is different …

[HTML][HTML] Study of associated genetic variants in Indian subjects reveals the basis of ethnicity related differences in susceptibility to venous thromboembolism

B Kumari, S Srivastava, T Chatterjee, R Vardhan… - Thrombosis, 2014 - hindawi.com
The genetic variants linked with the susceptibility of individuals to VTE are well known;
however, the studies explaining the ethnicity based difference in susceptibility to VTE are …

[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) …

Frequency of factor II G20210A, factor V Leiden, MTHFR C677T and PAI-1 5G/4G polymorphism in patients with venous thromboembolism: Croatian case-control …

Z Alfirevic, AM Simundic, N Nikolac, N Sobocan… - Biochemia …, 2010 - hrcak.srce.hr
Sažetak Introduction: Venous thromboembolic disease is one of the leading causes of
morbidity and mortality in the developed world. Identification of hereditary factors of …

Frequency of thrombophilic genetic polymorphisms among Saudi subjects compared with other populations

AA Settin, A Alghasham, A Ali, M Dowaidar, H Ismail - Hematology, 2012 - Taylor & Francis
Thrombophilic mutations increase the tendency toward thromboembolic disease. The aim of
this study was to estimate the prevalence of the genetic variants related to thrombophilia …

High prevalence of three prothrombotic polymorphisms among Palestinians: factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase C677T

AS Hussein - Journal of thrombosis and thrombolysis, 2012 - Springer
Abstract Factor V leiden G1691A/R506Q (FVL), prothrombin G20210A (FII) and
methylenetetrahydrofolate reductase (MTHFR) C677T are related genetic risk factors for …

The Saudi Thrombosis and Familial Thrombophilia Registry. Design, rational, and preliminary results.

JN Saour, MM Shoukri, LA Mammo - Saudi medical journal, 2009 - europepmc.org
Objective To describe the Registry and report preliminary data for the prevalence of 5
prothrombotic gene mutations in the normal Saudi population. Methods Blood from …

A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran

A Karimi, M Abolhasani… - Indian Journal of …, 2015 - journals.lww.com
Methods: A total of 35 DVT, 23 DVT/PE, and 37 PE patients admitted to the Hajar Hospital,
Shahrekord, Iran, between October 2009 and February 2011 were included in the study and …