Page last updated: 2024-10-17

coumarin and Factor X Deficiency

coumarin has been researched along with Factor X Deficiency in 1 studies

2H-chromen-2-one: coumarin derivative

Factor X Deficiency: Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Girolami, A1
Ruzza, G1
Cappellato, MG1
Vicarioto, MA1

Other Studies

1 other study available for coumarin and Factor X Deficiency

ArticleYear
Factor X antigen evaluation by means of a laser nephelometer in health and disease.
    Clinica chimica acta; international journal of clinical chemistry, 1985, May-30, Volume: 148, Issue:2

    Topics: Adult; Antigens; Coumarins; Factor X; Factor X Deficiency; Female; Heterozygote; Homozygote; Humans;

1985