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   Articles with "prothrombin g20210a" as a keyword



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Clinical significance of prothrombin G20210A mutation in homozygous patients

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recommendations! Published in 2017 at "American Journal of Hematology"

DOI: 10.1002/ajh.24859

Abstract: (P< .0001), low hemoglobin (P5 .0009), high absolute lymphocyte count (P5 .02), higher serum lactate dehydrogenase levels (P5 .023), PB blast % (P< .0001), BM blast % (P< .0001), 2016WHO morphological subtype CMML-2 (P< .0001),… read more here.

Keywords: g20210a mutation; significance prothrombin; prothrombin g20210a; mutation homozygous ... See more keywords

MTHFR (C677T, A1298C), FV Leiden polymorphisms, and the prothrombin G20210A mutation in arterial ischemic stroke among young tunisian adults.

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recommendations! Published in 2021 at "Metabolic brain disease"

DOI: 10.1007/s11011-020-00663-7

Abstract: Arterial ischemic stroke (AIS) in young adults is less common in older adults, but the underlying pathogenesis and risk factors are more multi-faceted. The role of inherited thrombophilia such as 5, 10-methylenetetrahydrofolate reductase (MTHFR) gene… read more here.

Keywords: risk; ischemic stroke; prothrombin g20210a; ais ... See more keywords

Prothrombin G20210A Gene Mutation-Induced Recurrent Deep Vein Thrombosis and Pulmonary Embolism: Case Report and Literature Review

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recommendations! Published in 2022 at "Journal of Investigative Medicine High Impact Case Reports"

DOI: 10.1177/23247096211058486

Abstract: Inherited thrombophilia is an important cause of venous thrombosis. The Factor V Leiden (FVL) is the most commonly encountered mutation, followed by the prothrombin G20210A gene mutation (PTM). The typical venous thrombotic events (VTEs) associated… read more here.

Keywords: gene mutation; prothrombin g20210a; case; mutation ... See more keywords

Frequency of three prothrombotic polymorphisms among Syrian population: factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase C677T

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recommendations! Published in 2017 at "Annals of Human Biology"

DOI: 10.3109/03014460.2015.1119308

Abstract: Abstract Background: Thrombophilia is a multi-factorial disorder caused by inherited and acquired factors. Among the inherited factors are factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase (MTHFR) C677T single nucleotide polymorphisms (SNPs). Aim: The main… read more here.

Keywords: c677t; prothrombin g20210a; g1691a prothrombin; syrian population ... See more keywords