SUMMARY ANSWER: Pregnant women with hereditary thrombophilia have an increased
risk of RPL, especially for pregnant women with the G1691A mutation of the factor V Leiden …

Background Thrombophilia is reported to be a candidate etiology of recurrent pregnancy
loss (RPL). No conclusive results on the association between prothrombin G20210A …

В обзоре рассматривается общая патологическая роль разнообразных форм
генетической тромбофилии в патогенезе множества осложнений беременности …

There are many genetic and acquired risk factors that are known to cause venous
thromboembolic disorders (VTE). One of these is the Prothrombin G20210A mutation, which …

Обследованы 143 беременных после ЭКО с проведением молекулярно-генетического
исследования. Изучен анализ ассоциацийполиморфизма тромбофилических генов …

Background Inherited antithrombin (AT) deficiency is a rare autosomal dominant disorder,
caused by mutations in the SERPINC1 gene. The most common clinical presentation in AT …

В настоящее время проблема гипергомоцистеинемии является предметом интереса
исследователей. Высокие концентрации гомоцистеина приводят к развитию …

Background Recurrent pregnancy loss (RPL) is a heterogeneous condition affecting up to
5% of women of reproductive age. Inherited thrombophilia have been postulated as one of …

Objective The aim of this study is to investigate whether Serpin clade C (SERPINC1), E-
selectin, P-selectin, Placental protein 13 (PP13), and Retinol-binding protein-4 (RBP4) …

Reproductive failure (recurrent foetal loss, unexplained infertility and IVF implantation
failure) may be, in a number of cases, explained by thrombophilia, either acquired or …