Thrombosis in rare bleeding disorders

Hematology

Volumn 17, Issue SUPPL. 1, 2012, Pages

  Ruiz Sáez, Arlette ^a  

^a National Haemophilia Center   (Venezuela)

Author keywords

Bleeding; Rare bleeding disorders; Thrombosis

Indexed keywords

ACTIVATED PROTHROMBIN COMPLEX; ANTITHROMBIN; BLOOD CLOTTING FACTOR 10; BLOOD CLOTTING FACTOR 11; BLOOD CLOTTING FACTOR 13; BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 7; FIBRINOGEN; PROTHROMBIN; RECOMBINANT BLOOD CLOTTING FACTOR 7A;

AFIBRINOGENEMIA; ARTERY OCCLUSION; ARTICLE; BLEEDING DISORDER; BLOOD CLOTTING FACTOR 11 DEFICIENCY; BLOOD CLOTTING FACTOR 7 DEFICIENCY; CENTRAL VENOUS CATHETER; DISEASE ASSOCIATION; DRUG ACTIVITY; DYSFIBRINOGENEMIA; FAMILIAL DISEASE; FIBRINOGEN DEFECT; GENETIC HETEROGENEITY; HEART INFARCTION; HEMOPHILIA A; HEMOPHILIA B; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; NONHUMAN; PATHOGENESIS; PREVALENCE; PRIORITY JOURNAL; RARE DISEASE; RISK FACTOR; SUBSTITUTION THERAPY; SURGICAL TECHNIQUE; SYMPTOMATOLOGY; THROMBOSIS; VON WILLEBRAND DISEASE;

BLOOD COAGULATION DISORDERS, INHERITED; FACTOR VII DEFICIENCY; FACTOR XI DEFICIENCY; FIBRINOGEN; HEMORRHAGE; HEMORRHAGIC DISORDERS; HUMANS; RARE DISEASES; THROMBOSIS;

EID: 84859767422     PISSN: 10245332     EISSN: 16078454     Source Type: Journal    
DOI: 10.1179/102453312X13336169156690     Document Type: Article

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