Reduced von Willebrand factor survival in von Willebrand disease: Pathophysiologic and clinical relevance

Journal of Thrombosis and Haemostasis

Volumn 7, Issue SUPPL. 1, 2009, Pages 71-74

  Castaman, Giancarlo ^a   Tosetto, A ^a   Rodeghiero, F ^a  

^a SAN BORTOLO HOSPITAL   (Italy)

Author keywords

Desmopressin; Inherited bleeding disorders; Von Willebrand disease; Von Willebrand factor

Indexed keywords

DESMOPRESSIN; GLYCOPROTEIN IB; RECOMBINANT BLOOD CLOTTING FACTOR 8; RECOMBINANT PROTEIN; RECOMBINANT VON WILLEBRAND FACTOR; UNCLASSIFIED DRUG; VON WILLEBRAND FACTOR; VON WILLEBRAND FACTOR CLEAVING PROTEINASE;

AMINO ACID SUBSTITUTION; BLOOD GROUP ABO SYSTEM; ENZYME ACTIVITY; GENE MUTATION; HUMAN; MACROPHAGE FUNCTION; NONHUMAN; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; PROTEIN DEGRADATION; PROTEIN FUNCTION; PROTEIN METABOLISM; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; PROTEIN SYNTHESIS; PROTEIN TARGETING; REVIEW; SURVIVAL TIME; THROMBOCYTE AGGREGATION; TREATMENT RESPONSE; VON WILLEBRAND DISEASE;

ABO BLOOD-GROUP SYSTEM; DEAMINO ARGININE VASOPRESSIN; HUMANS; MUTATION; VON WILLEBRAND DISEASES; VON WILLEBRAND FACTOR;

EID: 67849111584     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2009.03381.x     Document Type: Review

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