Inherited thrombophilias are not yet established as a cause of placenta-mediated pregnancy complications, such as fetal growth restriction, preeclampsia, abruption, and pregnancy loss. An inherited thrombophilia is only one of many factors that lead to development of these diseases and is unlikely to be the unique factor that should drive management in subsequent pregnancies. The paucity of evidence for benefit, coupled with a small potential for harm, suggests that low molecular weight heparin should be considered an experimental drug for these indications until data from controlled trials are published. At present, women with a history of placenta-mediated pregnancy complications, with or without a thrombophilia, should be followed closel...
Inherited thrombophilia is believed to be a multiple gene disease with more than one defect. We aime...
The aim of the study was to establish the importance of low molecular weight heparin (LMWH) treatmen...
Factor V Leiden represents a mutation in the gene coding the production of V factor, being the most ...
Inherited thrombophilias are not yet established as a cause of placenta-mediated pregnancy complicat...
There is a paucity of strong evidence associated with adverse pregnancy outcomes and thrombophilia i...
There is a paucity of strong evidence associated with adverse pregnancy outcomes and thrombophilia i...
Pregnancy may unmask an unrecognized thrombophilia with the development of venous thromboembolism (V...
Thrombophilias represent an evolving story that continues to stir controversy for care providers and...
The purpose of this study was to conduct a systematic review of the literature of studies that exami...
Abstract: There is a paucity of strong evidence associated with adverse pregnancy outcomes and throm...
BACKGROUND: As the placental vessels are dependent on the normal balance of procoagulant and antico...
BACKGROUND: As the placental vessels are dependent on the normal balance of procoagulant and antico...
Objective: Inherited thrombophilia is associated with thromboembolic events and/or poor obstetric ou...
Objective: Inherited thrombophilia is associated with thromboembolic events and/or poor obstetric ou...
Pregnancy is hypercoagulable state. The field of thrombophilia; the tendency to thrombosis, has been...
Inherited thrombophilia is believed to be a multiple gene disease with more than one defect. We aime...
The aim of the study was to establish the importance of low molecular weight heparin (LMWH) treatmen...
Factor V Leiden represents a mutation in the gene coding the production of V factor, being the most ...
Inherited thrombophilias are not yet established as a cause of placenta-mediated pregnancy complicat...
There is a paucity of strong evidence associated with adverse pregnancy outcomes and thrombophilia i...
There is a paucity of strong evidence associated with adverse pregnancy outcomes and thrombophilia i...
Pregnancy may unmask an unrecognized thrombophilia with the development of venous thromboembolism (V...
Thrombophilias represent an evolving story that continues to stir controversy for care providers and...
The purpose of this study was to conduct a systematic review of the literature of studies that exami...
Abstract: There is a paucity of strong evidence associated with adverse pregnancy outcomes and throm...
BACKGROUND: As the placental vessels are dependent on the normal balance of procoagulant and antico...
BACKGROUND: As the placental vessels are dependent on the normal balance of procoagulant and antico...
Objective: Inherited thrombophilia is associated with thromboembolic events and/or poor obstetric ou...
Objective: Inherited thrombophilia is associated with thromboembolic events and/or poor obstetric ou...
Pregnancy is hypercoagulable state. The field of thrombophilia; the tendency to thrombosis, has been...
Inherited thrombophilia is believed to be a multiple gene disease with more than one defect. We aime...
The aim of the study was to establish the importance of low molecular weight heparin (LMWH) treatmen...
Factor V Leiden represents a mutation in the gene coding the production of V factor, being the most ...