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The Journal of Laboratory and Clinical Medicine|February 1, 1979
Oxygen transport in a woman with hemoglobin Hope/beta+ thalassemiaS Charache, S Achuff, R Winslow, et al.Pediatric Research|July 1, 1979
The effect of hemoglobin F-Chesapeake (alpha 2 92 Arg. leads to Leu gamma 2) on fetal oxygen affinity and erythropoiesisC M Jones, S Charache, P J HathawayThe Journal of Laboratory and Clinical Medicine|January 1, 1985
Iron deficiency anemia: mitochondrial alpha-glycerophosphate dehydrogenase in guinea pig skeletal muscleV W Macdonald, S Charache, P J HathawayBritish Journal of Haematology|December 1, 1976
The Negro variety of hereditary persistence of fetal haemoglobin is a mild form of thalassaemiaS Charache, J B Clegg, D J WeatherallAmerican Journal of Hematology|October 1, 1989
Effect of hydroxyurea on the rheological properties of sickle erythrocytes in vivoS K Ballas, G J Dover, S CharacheAmerican Journal of Clinical Pathology|May 1, 1985
Laboratory evaluation of the Coulter "three-part electronic differential"L Nelson, S Charache, E Keyser, et al.Archives of Internal Medicine|October 1, 1985
A clinical trial of three-part electronic differential white blood cell countsS Charache, L Nelson, E Keyser, et al.American Journal of Clinical Pathology|May 1, 1989
Laboratory evaluation of differential white blood cell count information from the Coulter S-plus IV and Technicon H-1 in patient populations requiring rapid "turnaround" timeL Nelson, S Charache, S Wingfield, et al.American Journal of Clinical Pathology|February 1, 1995
Robotics in the hematology laboratory. An evaluation of the productivity of the Sysmex HS-330M Rothe, S Wingfield, P Barranco, et al.Obstetrics and Gynecology|April 1, 1980
Management of sickle cell disease in pregnant patientsS Charache, J Scott, J Niebyl, et al.Pageof 16