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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),…
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Keywords:
g20210a mutation;
significance prothrombin;
prothrombin g20210a;
mutation homozygous ... See more keywords
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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…
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Keywords:
risk;
ischemic stroke;
prothrombin g20210a;
ais ... See more keywords
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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…
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Keywords:
gene mutation;
prothrombin g20210a;
case;
mutation ... See more keywords
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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…
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Keywords:
c677t;
prothrombin g20210a;
g1691a prothrombin;
syrian population ... See more keywords