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The Journal of Laboratory and Clinical Medicine|April 1, 1987
Assessment of the hydration state of sickle cells by phthalate ester density distributionJ Kurantsin-Mills, H M Jacobs, L S LessinBlood|October 1, 1985
The acetylcholinesterase defect in paroxysmal nocturnal hemoglobinuria: evidence that the enzyme is absent from the cell membraneF L Chow, M J Telen, W F RosseBlood|December 1, 1982
Characterization of the IgG-Fc receptor on human plateletsS P Karas, W F Rosse, R J KurlanderThe Journal of Clinical Investigation|May 1, 1973
Mechanisms of immune lysis of red blood cells in vitro. I. Paroxysmal nocturnal hemoglobinuria cellsG L Logue, W F Rosse, J P AdamsThe Journal of Clinical Investigation|January 1, 1987
Interactions of the platelets in paroxysmal nocturnal hemoglobinuria with complement. Relationship to defects in the regulation of complement and to platelet survival in vivoD V Devine, R S Siegel, W F RosseAmerican Journal of Clinical Pathology|June 1, 1985
Presence of P blood group antigens on human plateletsR A Dunstan, M B Simpson, W F RosseTransfusion|May 1, 1984
Erythrocyte antigens on human platelets. Absence of Rh, Duffy, Kell, Kidd, and Lutheran antigensR A Dunstan, M B Simpson, W F RosseTransfusion|September 1, 1976
Hemolytic transfusion reactions caused by failure of commercial antiglobulin reagents to detect complementG K Sherwood, B F Haynes, W F RosseBlood|August 15, 1995
Immunophenotypic analysis of reticulocytes in paroxysmal nocturnal hemoglobinuriaR E Ware, W F Rosse, S E HallBritish Journal of Haematology|September 1, 1980
Subclasses of IgG antibodies in immune thrombocytopenic purpura (ITPO)W F Rosse, J P Adams, W J YountPageof 14