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S K Ballas

Showing results (1-10 of 189) with videos related to

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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 Ballas
American Journal of Clinical Pathology|April 1, 1979
Normal serum iron and elevated total iron-binding capacity in iron-deficiency statesS K Ballas
The Journal of Clinical Investigation|April 1, 1978
Abnormal erythrocyte membrane protein pattern in severe megaloblastic anemiaS K Ballas
Pediatric Pathology & Molecular Medicine|April 4, 2003
Effect of alpha-globin genotype on the pathophysiology of sickle cell diseaseS K Ballas
American Journal of Hematology|May 1, 1990
Treatment of pain in adults with sickle cell diseaseS K Ballas
Seminars in Hematology|February 24, 2001
Iron overload is a determinant of morbidity and mortality in adult patients with sickle cell diseaseS K Ballas
The New England Journal of Medicine|October 9, 1975
Letter: ESR and Coombs-positive hemolytic anemiaS K Ballas
The American Journal of the Medical Sciences|March 1, 1973
Sideroblastic refractory anemia in a patient with systemic lupus erythematosusS K Ballas
Postgraduate Medicine|May 1, 1974
Features of aplastic anemia in paroxysmal nocturnal hemoglobinuriaS K Ballas
Transfusion Medicine Reviews|July 1, 1990
The pathophysiology of hemolytic anemiasS K Ballas
Pageof 19

Showing results (1-10 of 189) with videos related to

Sort By:
Pageof 19
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 Ballas
American Journal of Clinical Pathology|April 1, 1979
Normal serum iron and elevated total iron-binding capacity in iron-deficiency statesS K Ballas
The Journal of Clinical Investigation|April 1, 1978
Abnormal erythrocyte membrane protein pattern in severe megaloblastic anemiaS K Ballas
Pediatric Pathology & Molecular Medicine|April 4, 2003
Effect of alpha-globin genotype on the pathophysiology of sickle cell diseaseS K Ballas
American Journal of Hematology|May 1, 1990
Treatment of pain in adults with sickle cell diseaseS K Ballas
Seminars in Hematology|February 24, 2001
Iron overload is a determinant of morbidity and mortality in adult patients with sickle cell diseaseS K Ballas
The New England Journal of Medicine|October 9, 1975
Letter: ESR and Coombs-positive hemolytic anemiaS K Ballas
The American Journal of the Medical Sciences|March 1, 1973
Sideroblastic refractory anemia in a patient with systemic lupus erythematosusS K Ballas
Postgraduate Medicine|May 1, 1974
Features of aplastic anemia in paroxysmal nocturnal hemoglobinuriaS K Ballas
Transfusion Medicine Reviews|July 1, 1990
The pathophysiology of hemolytic anemiasS K Ballas
Pageof 19