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Blood|March 1, 1977
Effects of ascorbic acid on glucose-6-phosphate dehydrogenase-deficient erythrocytes: studies in an animal modelT Udomratn, M H Steinberg, G D Campbell, et al.
The American Journal of the Medical Sciences|December 1, 1984
Interaction between HBS-beta-o-thalassemia and alpha-thalassemiaM H Steinberg, M B Coleman, J G Adams, et al.
Haematologia|January 1, 1984
Pure red blood cell aplasia associated with paraproteinemia: in vitro studies of erythropoiesisL Balducci, C Hardy, B Dreiling, et al.
Blood|March 15, 1993
Hydroxyurea increases fetal hemoglobin in cultured erythroid cells derived from normal individuals and patients with sickle cell anemia or beta-thalassemiaE Fibach, L P Burke, A N Schechter, et al.
Hemoglobin|April 13, 2001
Clinical and hematological responses to hydroxyurea in Sicilian patients with Hb S/beta-thalassemiaP Rigano, G P Rodgers, D Renda, et al.
British Journal of Haematology|January 1, 1981
Globin biosynthesis in erythroid bursts of heterozygous alpha or beta thalassaemiaM H Steinberg, M B Coleman, A Pressley, et al.
American Journal of Hematology|January 1, 1978
Erythroleukemia: in vitro studies of erythropoiesisM M Newcomb, L Balducci, M B Coleman, et al.
The Journal of Clinical Investigation|December 1, 1982
Spontaneous oxygen radical generation by sickle erythrocytesR P Hebbel, J W Eaton, M Balasingam, et al.
The Journal of Pediatrics|April 1, 1991
Neonatal screening for sickle cell disease: a cost-effectiveness analysisJ Tsevat, J B Wong, S G Pauker, et al.
The American Journal of the Medical Sciences|November 1, 1986
Effect of lead and ethanol upon gamma-globin synthesis in sickle reticulocytesJ G Adams, M V Newman, M H Steinberg, et al.
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