[HTML][HTML] Highlights on Genetic Polymorphism Associated with Thromboembolic Risk; Implications in Ophthalmic and Autoimmune Disorders—A Review

MO Romanitan, M Popa-Cherecheanu, VA Vasile… - Diagnostics, 2023 - mdpi.com
The present paper explores genetic polymorphism and its association with thromboembolic
retinal venous disorders, such as central/hemi-retinal vein occlusion, as well as possible …

Association of PAI-1 rs1799889 polymorphism with susceptibility to ischemic stroke: a huge meta-analysis based on 44 studies

M Jafari, MH Jarahzadeh, SA Dastgheib… - ACTA …, 2020 - karolinum.cz
Background: the PAI-1 rs1799889 polymorphism has been reported to be associated with
susceptibility to ischemic stroke. However, the results of previous studies have been …

Genetic polymorphism associated with thromboembolic risk in ophthalmic and autoimmune disorders: A case report

RA Pirvulescu, HT Stanca… - Experimental and …, 2021 - spandidos-publications.com
The aim of the present study was to discuss genetic polymorphism and its association with
thromboem‑bolic retinal venous disorders, such as central/hemi‑retinal vein occlusion …

[PDF][PDF] Патогенетическое обоснование применения комбинированного метода лечения тромбоза центральной вены сетчатки и ее ветвей (экспериментально …

АА Крылова - 2018 - 83.172.8.139
Актуальность темы исследования. Окклюзия центральной вены сетчатки (ЦВС) и ее
ветвей известна более 150 лет назад [198, 199], однако и в настоящее время …