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JMJ-Jamahiriya Medical Journal. 2006; 5 (2): 83-90
en Inglés | IMEMR | ID: emr-77559

RESUMEN

Inherited thrombophilia has been an area of intense clinical research since the description of deficiency of antithrombin III [1965], protein C [1981] and protein S [1985]. It is now possible to identify the inherited thrombophila in about 50% of cases of venous thrombosis. Certain components of inherited thrombophilia have a major impact on anticoagulant therapy, so basic knowledge about them is necessary in every medical speciality


Asunto(s)
Humanos , Antitrombina III , Proteína C , Proteína S , Factor V , Protrombina , Hiperhomocisteinemia , Cofactor II de Heparina , Trombomodulina/deficiencia , Lipoproteínas , Plasminógeno/deficiencia , alfa 2-Antiplasmina , Activador de Tejido Plasminógeno , Inhibidor 1 de Activador Plasminogénico , Carboxipeptidasa B2 , Factores de Coagulación Sanguínea
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