The bleeding diathesis in human glycogen storage disease type I: identification of a naturally occurring inhibitor of ristocetin-induced platelet aggregation
- 1 June 1980
- journal article
- research article
- Published by Elsevier in Thrombosis Research
- Vol. 18 (5) , 683-692
- https://doi.org/10.1016/0049-3848(80)90223-6
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Platelet receptors for human Factor VIII/von Willebrand protein: functional correlation of receptor occupancy and ristocetin-induced platelet aggregation.Proceedings of the National Academy of Sciences, 1979
- Demonstration and characterization of specific binding sites for factor VIII/von Willebrand factor on human platelets.Journal of Clinical Investigation, 1979
- Fibrinogen and ADP-induced platelet aggregationBlood, 1978
- Defect of platelet function associated with chronic hypoglycaemia.Archives of Disease in Childhood, 1976
- Impaired platelet function in glucose-6-phosphatase deficiencyThe Journal of Pediatrics, 1974
- Quantitative Assay of a Plasma Factor Deficient in von Willebrand's Disease that is Necessary for Platelet Aggregation. RELATIONSHIP TO FACTOR VIII PROCOAGULANT ACTIVITY AND ANTIGEN CONTENTJournal of Clinical Investigation, 1973
- PLATELET ABNORMALITIES IN VON WILLEBRAND'S DISEASE*Annals of the New York Academy of Sciences, 1972
- PLASMA PROTEIN REQUIREMENTS FOR HUMAN PLATELET AGGREGATIONAnnals of the New York Academy of Sciences, 1972
- THE BLEEDING DISORDER IN HEPATOMEGALIC FORMS OF GLYCOGEN STORAGE DISEASEActa Paediatrica, 1970
- THE HEMOSTATIC DEFECT IN GLYCOGEN STORAGE DISEASE, TYPE IActa Paediatrica, 1968