2B or not to be - The 45-year saga of the Montreal Platelet Syndrome

Thrombosis and Haemostasis

Volumn 104, Issue 5, 2010, Pages 903-910

  Poon, Man Chiu ^a   Rand, Margaret L ^b,c   Jackson, Shannon C ^d  

^a UNIVERSITY OF CALGARY   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c UNIVERSITY OF TORONTO   (Canada)

^d UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

Inherited coagulation disorders; Platelet pathology inherited and acquired; Thrombocytopenia; Von Willebrand disease; Von Willebrand factor

Indexed keywords

BLOOD CLOTTING FACTOR 8 CONCENTRATE; CALPAIN; TRANEXAMIC ACID; VON WILLEBRAND FACTOR;

BLEEDING TIME; BLOOD TRANSFUSION; CONFERENCE PAPER; DISEASE CLASSIFICATION; DISEASE COURSE; FLOW CYTOMETRY; GENE MUTATION; HUMAN; MONTREAL PLATELET SYNDROME; OUTCOME ASSESSMENT; PHENOTYPE; PRIORITY JOURNAL; THROMBOCYTE ACTIVATION; THROMBOCYTE AGGLUTINATION; THROMBOCYTE AGGREGATION; THROMBOCYTE COUNT; THROMBOCYTE DISORDER; THROMBOCYTE SHAPE; THROMBOCYTOPENIA; TRANSMISSION ELECTRON MICROSCOPY; VON WILLEBRAND DISEASE;

BLOOD COAGULATION; BLOOD COAGULATION TESTS; BLOOD PLATELET DISORDERS; BLOOD PLATELETS; CANADA; GENETIC PREDISPOSITION TO DISEASE; HISTORY, 20TH CENTURY; HUMANS; MUTATION; PEDIGREE; PHENOTYPE; PLATELET FUNCTION TESTS; SYNDROME; VON WILLEBRAND DISEASE, TYPE 2; VON WILLEBRAND FACTOR;

EID: 78149487139     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1160/TH10-01-0079     Document Type: Conference Paper

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