CLASSIFICATION OF VON WILLEBRAND'S DISEASE
- 1 December 1978
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 312 (8104) , 1364-1365
- https://doi.org/10.1016/s0140-6736(78)91992-x
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
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- Dissociation between Factor VIII (Activity and Antigen) and Ristocetin-Induced Platelet Aggregation in von Willebrand’s DiseaseActa Haematologica, 1975
- WILLEBRAND-FACTOR ACTIVITY AND ANTIGEN IN VON WILLEBRAND'S DISEASEThe Lancet, 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
- Two Genetic Variants of von Willebrand's DiseaseNew England Journal of Medicine, 1973
- Genetic Variants of von Willebrand's DiseaseBMJ, 1972
- Lyophilized Plasma as an Assay Standard for Factor VIII: Calibration and Control with Fresh Plasma SamplesBritish Journal of Haematology, 1970
- Biological findings in Von Willebrand's pedigrees: implications for inheritanceJournal of Clinical Pathology, 1967
- The Plasma Concentration of Factor VIII in the Normal PopulationBritish Journal of Haematology, 1964
- The Investigation of a Large Family Affected with von Willebrand's DiseaseArchives of Disease in Childhood, 1954