Paradoxical thrombosis part 1: Factor replacement therapy, inherited clotting factor deficiencies and prolonged APTT

Journal of Thrombosis and Thrombolysis

Volumn 34, Issue 3, 2012, Pages 360-366

  Lippi, Giuseppe ^a   Favaloro, Emmanuel J ^b   Franchini, Massimo ^c  

^a UNIVERSITY HOSPITAL OF PARMA   (Italy)

^b CARLO POMA HOSPITAL   (Italy)

^c WESTMEAD HOSPITAL   (Australia)

Author keywords

Atypical; Haemophilia; Paradoxical; Pathogenesis; Thrombosis; Von Willebrand disease

Indexed keywords

ACTIVATED PROTHROMBIN COMPLEX; BETA2 GLYCOPROTEIN 1 ANTIBODY; BLOOD CLOTTING FACTOR 12; BLOOD CLOTTING FACTOR 7; BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 8 CONCENTRATE; BLOOD CLOTTING FACTOR 8 PLUS VON WILLEBRAND FACTOR; BLOOD CLOTTING FACTOR 9 CONCENTRATE; BLOOD CLOTTING FACTOR CONCENTRATE; CARDIOLIPIN ANTIBODY; FIBRINOGEN; LA ANTIBODY; LUPUS ANTICOAGULANT; PHOSPHOLIPID ANTIBODY; RECOMBINANT BLOOD CLOTTING FACTOR 7A;

ANTIPHOSPHOLIPID SYNDROME; ARTERIAL THROMBOEMBOLISM; ARTERY THROMBOSIS; ARTICLE; BLOOD CLOTTING FACTOR 12 DEFICIENCY; BLOOD CLOTTING FACTOR 7 DEFICIENCY; BLOOD CLOTTING FACTOR DEFICIENCY; CLINICAL TRIAL (TOPIC); DEEP VEIN THROMBOSIS; DISEASE ASSOCIATION; HEMOPHILIA; HEMOPHILIA A; HEMOPHILIA B; HUMAN; HYPOFIBRINOGENEMIA; MULTICENTER STUDY (TOPIC); PARADOXICAL DRUG REACTION; PARADOXICAL THROMBOSIS; PARTIAL THROMBOPLASTIN TIME; PREVALENCE; PRIORITY JOURNAL; SUPERFICIAL THROMBOPHLEBITIS; THROMBOEMBOLISM; THROMBOSIS; UNSTABLE ANGINA PECTORIS; VEIN THROMBOSIS; VENOUS THROMBOEMBOLISM; VON WILLEBRAND DISEASE;

BLOOD COAGULATION DISORDERS, INHERITED; BLOOD COAGULATION FACTORS; EMBOLISM, PARADOXICAL; HUMANS; LUPUS COAGULATION INHIBITOR; PARTIAL THROMBOPLASTIN TIME;

EID: 84868450162     PISSN: 09295305     EISSN: 1573742X     Source Type: Journal    
DOI: 10.1007/s11239-012-0753-3     Document Type: Article

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