Congenital Disorders of Platelet Function
- 1 February 1990
- journal article
- review article
- Published by Elsevier in Hematology/Oncology Clinics of North America
- Vol. 4 (1) , 65-86
- https://doi.org/10.1016/s0889-8588(18)30506-9
Abstract
No abstract availableKeywords
This publication has 99 references indexed in Scilit:
- Gray platelet syndrome. Demonstration of alpha granule membranes that can fuse with the cell surface.Journal of Clinical Investigation, 1987
- ATP‐ADP compartmentation in storage pool deficient platelets: correlation between granule‐bound ADP and the bleeding timeBritish Journal of Haematology, 1983
- Incidence of Severe von Willebrand's DiseaseNew England Journal of Medicine, 1982
- Familial Bleeding Tendency with Partial Platelet Thromboxane Synthetase Deficiency: Reorientation of Cyclic Endoperoxide MetabolismBritish Journal of Haematology, 1981
- CONGENITAL DEFICIENCY OF THROMBOXANE AND PROSTACYCLINThe Lancet, 1980
- SEVERE BLEEDING ASSOCIATED WITH DEFECTIVE THROMBOXANE SYNTHETASEThe Lancet, 1980
- Complete Correction of the Wiskott-Aldrich Syndrome by Allogeneic Bone-Marrow TransplantationNew England Journal of Medicine, 1978
- A molecular defect in thrombasthenic platelets.Journal of Clinical Investigation, 1975
- Hereditary Giant Platelet SyndromeBritish Journal of Haematology, 1975
- Impaired platelet function in glucose-6-phosphatase deficiencyThe Journal of Pediatrics, 1974