MedicineGeneticsHematologyHemostasisImmunogeneticsImmunopathologyCoagulation AbnormalitiesCoagulation DisordersGenetic DisordersInherited Disease TestingPlatelet DisordersVon Willebrand DiseaseFactor Viii AlterationsRistocetin Cofactor AssayVon Willebrand Disease DiagnosisVon Willebrand Factor Activity AssaysVon Willebrand Factor AntigenVon Willebrand Factor DisordersVon Willebrand Factor Function
Three patients with severe Von Willebrand's disease are shown to be homozygotes. They were born from unaffected parents. New techniques using a factor-VIII-related antigen assay by the Laurell method and a ristocetin-induced platelet aggregation assay demonstrated abnormalities in these two tests in both parents of the probands. Factor-VIII-related of heterogotes could not be differentiated from normal factor-VIII-related antigen by the immunodiffusion technique, crossed immunoelectrophoresis, and filtration on a sepharose 4b column.
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Antigen-antibody crossed electrophoresis
C.‐B. Laurell · Analytical Biochemistry · 1965 · 1.4K citations
Harvey J. Weiss, Leon W. Hoyer, Frederick R. Rickles et al. · Journal of Clinical Investigation · 1973 · 425 citations · Full text
Medicine, Hematology, Pathology +17
Platelet Adhesiveness in von Willebrand’s Disease
E. J. Walter Bowie, Charles A. Owen, John H. Thompson et al. · American Journal of Clinical Pathology · 1969 · 190 citations
Medicine, Hematology, Pathology +17