Increased von willebrand factor (vWF) binding to platelets associated with impaired vWF breakdown in thrombotic thrombocytopenic purpura

Journal of Clinical Apheresis

Volumn 13, Issue 3, 1998, Pages 126-132

  Moake, Joel L ^a,b,c   Chow, Thomas W ^b  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b Rice University   (United States)

^c Main Bldg ^*  (United States)

Author keywords

Thrombotic thrombocytopenic purpura (TTP); Unusually large vWf; von Willebrand factor (vWf); vWf metalloproteinase

Indexed keywords

METALLOPROTEINASE; VON WILLEBRAND FACTOR;

CONFERENCE PAPER; ENZYME DEFICIENCY; HUMAN; PROTEIN DEGRADATION; PROTEIN PROCESSING; PROTEIN SYNTHESIS; RELAPSE; SHEAR STRESS; THROMBOCYTE AGGREGATION; THROMBOTIC THROMBOCYTOPENIC PURPURA;

ADULT; BLOOD PLATELETS; CHILD; CHILD, PRESCHOOL; HUMANS; PURPURA, THROMBOCYTOPENIC; RECURRENCE; VON WILLEBRAND FACTOR;

EID: 0031733409     PISSN: 07332459     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1101(1998)13:3<126::AID-JCA6>3.0.CO;2-U     Document Type: Conference Paper

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