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The Journal of Pediatrics|May 1, 1997
Umbilical cord blood stem cells: application for the treatment of patients with hemoglobinopathiesP Kelly, J Kurtzberg, E Vichinsky, et al.
Blood|November 1, 1981
The diagnosis of iron deficiency anemia in sickle cell diseaseE Vichinsky, K Kleman, S Embury, et al.
Experimental Hematology|January 1, 1984
Evidence for a heterogeneous response to erythropoietin in the CFUE pool of human bone marrowR Pennathur-Das, E Alpen, E Vichinsky, et al.
Annals of the New York Academy of Sciences|January 1, 1982
Peroxidation, vitamin E, and sickle-cell anemiaD Chiu, E Vichinsky, M Yee, et al.
Pediatrics|June 1, 1988
Newborn screening for sickle cell disease: effect on mortalityE Vichinsky, D Hurst, A Earles, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Universal screening for hemoglobinopathies using high-performance liquid chromatography: clinical results of 2.2 million screensF Lorey, G Cunningham, F Shafer, et al.
Blood|May 1, 1984
Evidence for the presence of CFU-E with increased in vitro sensitivity to erythropoietin in sickle cell anemiaR Pennathur-Das, E Alpen, E Vichinsky, et al.
International Journal of Laboratory Hematology|November 19, 2009
Application of an expanded multiplex genotyping assay for the simultaneous detection of Hemoglobin Constant Spring and common deletional alpha-thalassemia mutationsJ L Kidd, M Azimi, B Lubin, et al.
The Journal of Pediatrics|May 1, 1992
Differentiation of homozygous hemoglobin E from compound heterozygous hemoglobin E-beta O-thalassemia by hemoglobin E mutation analysisJ P Johnson, E Vichinsky, D Hurst, et al.
Blood|May 29, 2000
Evidence for HLA-related susceptibility for stroke in children with sickle cell diseaseL A Styles, C Hoppe, W Klitz, et al.
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