Results 61 to 70 of about 27,558 (226)
Thrombophilia and Hypercoagulability [PDF]
This is a review of less well-known aspects of thrombophilia and hypercoagulability as they relate to thrombosis. Thrombosis is an abnormal fibrin clot that develops in circulating blood with clinical symptoms of one or more arterial and/or venous obstructions exclusively identified by imaging techniques.
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ABSTRACT Paroxysmal nocturnal hemoglobinuria (PNH) is a rare hematologic disorder caused by a defect of glycosylphosphatidyl‐anchored proteins, leading to an uncontrolled complement‐mediated hemolysis. The advent of complement inhibitors in clinical practice radically changed patients' outcomes and survival.
Bruno Fattizzo +8 more
wiley +1 more source
Thrombophilia and the Placenta
This chapter contains sections titled: Introduction Inheritable thrombophilia Acquired thrombophilia Adverse pregnancy outcomes Thrombotic locations Diagnosis, management, and treatment ...
Paidas, Michael J +3 more
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Mechanisms of thrombophilia [PDF]
Editorial.-- El pdf es la versión post-print.
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Prevalence of hereditary thrombophilia among Egyptian children with portal vein thrombosis
Background Portal vein thrombosis (PVT) is an important cause of portal hypertension in the pediatric age group with high morbidity rates due to its main complication—the upper gastrointestinal varices and hypersplenism.
Iman Mohamed Talaat +6 more
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Introduction: In Denmark, 10 % of new-borns are being conceived with the aid of medically assisted reproduction (MAR). MAR can imply induction of high levels of oestradiol, which in turn leads to increased coagulation activity, decreased natural ...
Jesper Strandberg +5 more
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The aim of the study was to establish the importance of low molecular weight heparin (LMWH) treatment for good pregnancy outcome in patients with hereditary thrombophilia.
Vesna Sokol +3 more
doaj +1 more source
Thromboembolism (TE) is a complex disease caused by various acquired and inherited factors. The common mutations; factor V Leiden G1691A (FVL G1691A), prothrombin G20210A (PTG20210A), and methylene tetrahydrofolate reductase C677T (MTHFR C677T) are ...
Ali Ibrahim Mohammed MD, FICMS +3 more
doaj +1 more source
ABSTRACT Introduction The 2024 ISTH clinical practice guideline (CPG) for treatment of congenital haemophilia, the NBDF‐McMaster Guideline on Care Models for Haemophilia Management, and ASH ISTH NBDF WFH guidelines on the diagnosis and management of VWD all utilised GRADE methodology.
Mark W. Skinner +59 more
wiley +1 more source
The term “thrombophilia” is generally used to designate states of hypercoagulability caused by an inherent abnormality of the coagulation system, resulting in an increased risk of thrombosis.
Simon Mantha +3 more
core +1 more source

