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American Journal of Hematology|February 1, 1991
Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of dense cellsS K BallasAmerican Journal of Clinical Pathology|April 1, 1979
Normal serum iron and elevated total iron-binding capacity in iron-deficiency statesS K BallasThe Journal of Clinical Investigation|April 1, 1978
Abnormal erythrocyte membrane protein pattern in severe megaloblastic anemiaS K BallasPediatric Pathology & Molecular Medicine|April 4, 2003
Effect of alpha-globin genotype on the pathophysiology of sickle cell diseaseS K BallasAmerican Journal of Hematology|May 1, 1990
Treatment of pain in adults with sickle cell diseaseS K BallasSeminars in Hematology|February 24, 2001
Iron overload is a determinant of morbidity and mortality in adult patients with sickle cell diseaseS K BallasAnnals of Clinical and Laboratory Science|July 1, 1992
Munchausen sickle cell painful crisisS K BallasAmerican Journal of Hematology|December 1, 1996
Factitious sickle cell acute painful episodes: a secondary type of Munchausen syndromeS K BallasTransfusion|March 1, 1981
Red cell membrane protein changes caused by freezing and the mechanism of cryoprotection by glycerolS K BallasCleveland Clinic Journal of Medicine|February 2, 1999
Complications of sickle cell anemia in adults: guidelines for effective managementS K BallasPageof 19