Risk factors for ischemic stroke in younger adults: a focused update

MG George - Stroke, 2020 - Am Heart Assoc
730 Stroke March 2020 migraine with aura is associated with an≈ 2-fold increase in risk of
ischemic stroke. 20, 21 However, the combination of all 3 risk factors (migraine with aura …

Genetic risk factors in venous thromboembolism

C Hotoleanu - Thrombosis and Embolism: from Research to Clinical …, 2017 - Springer
Genetic risk factors predispose to thrombophilia and play the most important etiopathogenic
role in venous thromboembolism (VTE) in people younger than 50 years old. At least one …

[HTML][HTML] Potential genes associated with COVID-19 and comorbidity

S Feng, F Song, W Guo, J Tan, X Zhang… - … journal of medical …, 2022 - ncbi.nlm.nih.gov
Hypertension, diabetes mellitus, and coronary artery disease are common comorbidities and
dangerous factors for infection and serious COVID-19. Polymorphisms in genes associated …

[HTML][HTML] Inherited and acquired thrombophilia in adults with retinal vascular occlusion: A systematic review and meta‐analysis

GF Romiti, B Corica, M Borgi, G Visioli, E Pacella… - Journal of Thrombosis …, 2020 - Elsevier
Background Retinal vascular occlusion is a leading cause of sight loss. Both retinal artery
occlusion (RAO) and retinal vein occlusion (RVO) have been associated with …

Ethnic diversity in the genetics of venous thromboembolism

L Tang, Y Hu - Thrombosis and haemostasis, 2015 - thieme-connect.com
Genetic susceptibility is considered as a crucial factor for the development of venous
thromboembolism (VTE). Epidemiologic and genetic studies have revealed clear disparities …

An overview of thrombophilia and associated laboratory testing

M Montagnana, G Lippi, E Danese - Hemostasis and Thrombosis …, 2017 - Springer
Venous thromboembolism, usually entailing deep vein thrombosis, pulmonary embolism, or
both, is a complex and multifactorial disorder, in which a number of putative conditions …

Prothrombin G20210A gene mutation-induced recurrent deep vein thrombosis and pulmonary embolism: case report and literature review

S Elkattawy, R Alyacoub, KS Singh… - … High Impact Case …, 2022 - journals.sagepub.com
Inherited thrombophilia is an important cause of venous thrombosis. The Factor V Leiden
(FVL) is the most commonly encountered mutation, followed by the prothrombin G20210A …

[HTML][HTML] Thrombophilia genetic mutations and their relation to disease severity among patients with COVID-19

H Moness, SO Mousa, SO Mousa, NM Adel… - Plos one, 2024 - journals.plos.org
Objectives Patients with COVID-19 infection appear to develop virus-induced
hypercoagulability resulting in numerous thrombotic events. The aim of the present study …

Genetic risk factors in thrombotic primary antiphospholipid syndrome: A systematic review with bioinformatic analyses

MA Islam, SS Khandker, F Alam, MA Kamal… - Autoimmunity Reviews, 2018 - Elsevier
Abstract Background Antiphospholipid Syndrome (APS) is an autoimmune multifactorial
disorder. Genetics is believed to play a contributory role in the pathogenesis of APS …

Therapeutic implications of inherited thrombophilia in pregnancy

LF Trasca, N Patrascu, R Bruja… - American Journal of …, 2019 - journals.lww.com
Background: Inherited (hereditary) thrombophilia is a genetic disorder that affects
coagulation, being responsible for more than 60% of idiopathic (spontaneous or …