Spectrum of changes in endogenous thrombin potential due to heritable disorders of coagulation

Blood Coagulation and Fibrinolysis

Volumn 19, Issue 6, 2008, Pages 577-580

  Ghosh, Kanjaksha ^a   Mota, Leenam ^a   Shetty, Shrimati ^a   Kulkarni, Bipin ^a  

^a KEM HOSPITAL   (India)

Author keywords

Endogenous thrombin potential; Heritable disorders of coagulation; Pattern of thrombin generation

Indexed keywords

BLOOD CLOTTING FACTOR 10; BLOOD CLOTTING FACTOR 11; BLOOD CLOTTING FACTOR 12; BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 7; BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9; THROMBIN; VITAMIN K GROUP; BLOOD CLOTTING FACTOR 10A; PROTHROMBINASE COMPLEX; UNCLASSIFIED DRUG;

AREA UNDER THE CURVE; ARTICLE; BLEEDING; BLOOD CLOTTING DISORDER; BLOOD CLOTTING FACTOR 11 DEFICIENCY; BLOOD CLOTTING FACTOR 12 DEFICIENCY; BLOOD CLOTTING FACTOR 5 DEFICIENCY; BLOOD CLOTTING FACTOR 7 DEFICIENCY; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; ECCHYMOSIS; EPISTAXIS; HEMOPHILIA A; HEMOPHILIA B; HUMAN; MAJOR CLINICAL STUDY; PARAMETER; PRIORITY JOURNAL; VITAMIN K DEFICIENCY; BIOSYNTHESIS; BLOOD; COMPARATIVE STUDY; GENETICS; METABOLISM; TIME;

AREA UNDER CURVE; BLOOD COAGULATION DISORDERS, INHERITED; COAGULATION PROTEIN DISORDERS; FACTOR V; FACTOR XA; HEMORRHAGE; HUMANS; THROMBIN; TIME FACTORS;

EID: 58149111253     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/MBC.0b013e328307089d     Document Type: Article

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