An inherited bleeding disorder linked to a defective interaction between ADP and its receptor on platelets. Its influence on glycoprotein IIb-IIIa complex function

Journal of Clinical Investigation

Volumn 95, Issue 4, 1995, Pages 1612-1622

  Nurden, P ^a   Savi, P ^a   Heilmann, E ^a   Bihour, C ^a   Herbert, J M ^a   Maffrand , J P ^a   Nurden, A ^a  

^a HAUT LÉVÊQUE HOSPITAL   (France)

Author keywords

ADP receptor; flow cytometry; inherited disorder; platelet activation; platelet aggregation

Indexed keywords

ADENOSINE DIPHOSPHATE; ADENYLATE CYCLASE; ADRENALIN; CYCLIC AMP; FIBRINOGEN RECEPTOR; GLYCOPROTEIN IIB; GLYCOPROTEIN IIIA; MONOCLONAL ANTIBODY; PROSTAGLANDIN E1; THROMBOCYTE RECEPTOR;

ADULT; ARTICLE; BLEEDING DISORDER; CASE REPORT; FLOW CYTOMETRY; GENETIC DISORDER; GLANZMANN DISEASE; HUMAN; HUMAN CELL; MALE; PRIORITY JOURNAL; THROMBOCYTE ACTIVATION; THROMBOCYTE AGGREGATION; THROMBOCYTE FUNCTION;

EID: 0028942659     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI117835     Document Type: Article

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