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Cytometry|September 1, 1988
Flow cytometric analysis of platelet surface antigensG E Marti, L Magruder, W E Schuette, et al.Blood|July 1, 1986
DDAVP infusion in five patients with type Ia glycogen storage disease and associated correction of prolonged bleeding timesG E Marti, M E Rick, J Sidbury, et al.The Journal of Laboratory and Clinical Medicine|March 1, 1989
Subendothelial matrix of cultured endothelial cells contains fully processed high molecular weight von Willebrand factorS H Tannenbaum, M E Rick, B Shafer, et al.The Journal of Biological Chemistry|March 5, 1986
von Willebrand factor binds specifically to sulfated glycolipidsD D Roberts, S B Williams, H R Gralnick, et al.The American Journal of Medicine|October 1, 1977
Blast crisis of chronic granulocytic leukemia. Morphologic variants and therapeutic implicationsS Rosenthal, G P Canellos, J Whang-Peng, et al.Blood|August 1, 1982
Factor VIII/von Willebrand factor binding to von Willebrand's disease plateletsH R Gralnick, S B Williams, B C Shafer, et al.Blood|May 1, 1977
Characteristics of blast crisis in chronic granulocytic leukemiaS Rosenthal, G P Canellos, V T DeVita, et al.The Journal of Clinical Investigation|September 1, 1971
Fibrinogen Bethesda: a congenital dysfibrinogenemia with delayed fibrinopeptide releaseH R Gralnick, H M Givelber, J R Shainoff, et al.Thrombosis Research|May 1, 1982
The identification and functional significance of factor VIII components on normal plateletsM A Flaum, J A Donlon, H R Gralnick, et al.Thrombosis and Haemostasis|March 2, 1992
Absence of the largest platelet-von Willebrand multimers in a patient with lactoferrin deficiency and a bleeding tendencyR I Parker, L P McKeown, J I Gallin, et al.Pageof 15