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contentuptodate· Content· item f13_2_13358

©2013 UpToDate ® Print Email Apoptosis in thalassemia variants These graphs show the percentage of erythroid precursors undergoing apoptosis (mean ± 1 SD) in normal controls and in patients from Thailand with clinical diagnoses of α and β thalassemia, using both the annexin V and the Hoechst 33342 methodologies. hbH: hemoglobin H disease; H/CS: hemoglobin H/hemoglobin constant spring; CS/CS: homozygous hemoglobin constant spring; bthal/hbE: beta thalassemia/hemoglobin E disease. Reproduced with permission from: Pootrakul, P, et al. Blood 2000; 96:2610. Copyright © 2000 American Society of Hematology.