Charache, Samuel

Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia

Charache, S., Terrin, M. L., Moore, R. D., Dover, G. J., Barton, F. B., Eckert, S. V., McMahon, R. P., & Bonds, D. R. (1995) · New England Journal of Medicine

Hemoglobinopathies and Related DisordersBlood groups and transfusion

Cited by 2,340

Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea

Steinberg, M. H., Lu, Z.-H., Barton, F. B., Terrin, M. L., Charache, S., Dover, G. J., & Hydroxyurea, T. M. S. O. (1997) · Blood

Hemoglobinopathies and Related DisordersBlood groups and transfusion

Cited by 407

Individual variation in the production and survival of F cells in sickle-cell disease

Dover, G. J., Boyer, S. H., Charache, S., & Heintzelman, K. (1978) · New England Journal of Medicine

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 144

Hb Potomac (101 Glu replaced by Asp): speculations on placental oxygen transport in carriers of high-affinity hemoglobins

Charache, S., Jacobson, R., Brimhall, B., Murphy, E., Hathaway, P., Winslow, R., Jones, R., Rath, C., & Simkovich, J. (1978) · Blood

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 49

'Acute Chest Syndrome' in Adults With Sickle Cell Anemia: Microbiology, Treatment, and Prevention

Charache, S. (1979) · Archives of Internal Medicine

Hemoglobinopathies and Related DisordersPneumonia and Respiratory Infections

Cited by 0