MOLECULAR DEFECTS IN HÆMOPHILIA A AND VON WILLEBRAND'S DISEASE
- 1 April 1976
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 307 (7964) , 837-838
- https://doi.org/10.1016/s0140-6736(76)90485-2
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Studies of the human factor VIII/von Willebrand factor protein. III. Qualitative defects in von Willebrand's disease.Journal of Clinical Investigation, 1975
- Detection of heterozygotes in both parents of homozygous patients with Von Willebrand's disease.Journal of Clinical Pathology, 1975
- MOLECULAR STRUCTURAL STUDIES OF HUMAN FACTOR VIII*Annals of the New York Academy of Sciences, 1975
- A Variant of Factor VIII Related AntigenBritish Journal of Haematology, 1974
- Von Willebrand Factor: Dissociation from Antihemophilic Factor Procoagulant ActivityScience, 1973
- Studies on the Nature of Antihemophilic Factor (Factor VIII)Journal of Clinical Investigation, 1973
- FACTOR VIIIThe Lancet, 1973
- Studies on the Response of Patients with Classic Hemophilia to Transfusion with Concentrates of Antihemophilic FactorJournal of Clinical Investigation, 1972
- Transfusion Studies in von Willebrand's Disease: Effect on Bleeding Time and Factor VIIIBritish Journal of Haematology, 1963
- On an Inherited Autosomal Hemorrhagic Diathesis with Antihemophilic Globulin (AHG) Deficiency and Prolonged Bleeding Times1Acta Medica Scandinavica, 1957