Results 31 to 40 of about 6,414 (212)
Thrombophilia or hypercoagulable state is a predisposition to form clots. Thrombophilia can be inherited or acquired, and prevalently involves venous vessels.
Federico Cacciapuoti
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It is uncertain whether the JAK2 V617F mutation increases the thrombotic risk in patients with essential thrombocythemia, and it is unknown whether inherited thrombophilia is an additive risk factor in mutated subjects.
Valerio De Stefano +8 more
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Heritable Thrombophilia in Venous Thromboembolism in Northern Pakistan: A Cross-Sectional Study
Background. Venous thromboembolism (VTE) is referred to as formation of clots in a deep vein or lodging of thrombus towards the lungs which could be fatal yet preventable. The risk of developing VTE can be increased by various factors.
Maria Khan +4 more
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Background and Objectives: The diagnostic value of thrombophilia remains unknown in young patients with patent foramen ovale (PFO) and stroke. In this study we hypothesized that inherited thrombophilias that lead to venous thrombosis are more prevalent ...
Mantas Jokubaitis +6 more
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In January 2020, SARS-COV-2 infection spread worldwide and was declared “pandemic” by WHO. Because of the high contagiousness of the virus and devastating effects of the epidemic on public health, numerous efforts have been made to develop suitable ...
Federica Mele +10 more
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Combined thrombophilia is known as a probable cause of recurrent in vitro fertilization (IVF) failures. The present clinical case demonstrates the importance of considering the possibility of inherited or acquired thrombophilia in patients under the ...
N. S. Stuleva +2 more
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One of the most important aspects of reducing the incidence of preeclampsia is the most complete and timely assessment of risk factors for each patient. One of the well-known, but often overlooked, risk factors is a family history of preeclampsia. In the
Lidiya O. Buzyan
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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
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Demographic, clinical, and genetic evaluation of patients with suspected inherited thrombophilia
INTRODUCTION: Inherited and acquired disorders of hemostasis cause thrombophilia. Thrombosis occurs earlier in individuals with multiple inherited hemostatic disorders.
Pınar Tosun Taşar +5 more
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Here we describe a clinical case of successfully managed pregnancy and labor in female with multigenic thrombophilia (combination of homozygous Leiden and heterozygous prothrombin G20210A mutations) associated with high risk of thrombosis by using proper
M. O. Arslanbekova, J. Kh. Khizroeva
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