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American Journal of Hematology|December 1, 1982
The effect of cell hydration on the deformability of normal and sickle erythrocytesM L Gulley, D W Ross, C Feo, et al.Annals of Surgery|January 1, 1986
Hereditary spherocytosis. Recent experience and current concepts of pathophysiologyR D Croom, C W McMillan, E P Orringer, et al.Archives of Internal Medicine|September 1, 1976
Hemolysis caused by factor VIII concentratesE P Orringer, M J Koury, P M Blatt, et al.American Journal of Clinical Pathology|September 1, 1980
Pappenheimer bodies. An additional cause for a spurious platelet countB D Morton, E P Orringer, L A LaHart, et al.JAMA|November 22, 2001
Purified poloxamer 188 for treatment of acute vaso-occlusive crisis of sickle cell disease: A randomized controlled trialE P Orringer, J F Casella, K I Ataga, et al.Cancer|October 15, 1987
Granulocytic sarcoma presenting as pulmonary nodules and lymphadenopathyM Callahan, S Wall, F Askin, et al.The Journal of Burn Care & Rehabilitation|March 1, 1992
Causes and time course of acute hemolysis after burn injury in the ratY Endoh, M Kawakami, E P Orringer, et al.American Journal of Hematology|January 1, 1992
Physiologic and rheologic effects of the antisickling agent ethacrynic acid and its N-butylated derivative on normal and sickle erythrocytesE P Orringer, D S Blythe, J A Whitney, et al.Molecular Pharmacology|May 29, 1999
Detection of nitrosyl hemoglobin in venous blood in the treatment of sickle cell anemia with hydroxyureaR E Glover, E D Ivy, E P Orringer, et al.Southern Medical Journal|January 1, 1986
Cholelithiasis in sickle cell anemia: surgical considerationsR Rutledge, R D Croom, J W Davis, et al.Pageof 7