… chain, which may be another sickle cell β chain (in which case the patient is homozygous
Hb SS and by definition has sickle cell anemia), Hb SC, or one of the thalassemias (Hb S-thal). …

… sickle hemoglobin (Hb S) variant and its relation to sickle cell disease. To that end, the MEDLINE
literature search strategy used for this review was: sickle cell [… which sickle cell disease …

… hemoglobin, even in its deoxy state. In this chapter we briefly consider the available treatment
procedures of sickle cell anemia … be an effective therapeutic strategy for sickle cell anemia. …

… electrophoretic mobilities of sickle cell anemia hemoglobin and normal hemoglobin differ, we
… 1 percent more of the sickle cell anemia component than did the sickle cell trait material. 8q …

… polymerization in solutions and in red cells. The polymerization of sickle cell hemoglobin …
The structure of the hemoglobin S molecule, the structure of the various aggregated forms of …

… severe anemia, characterized by certain peculiar morphologic alterations of the red blood
cells, … changes, and Cook and Meyer 3 reported the third example of this rare type of anemia. …

… of fetal hemoglobin (HbF;α2γ2) in sickle cell disease started … Watson confirmed that infants
with sickle cell disease had few … to sickle and did not deform as extensively as did their sickle …

… Sickle Cell Hemoglobin C Disease. He stated "the peculiar retinopathy and vitreous hemorrhage
occurs almost always in the sickle cell hemoglobin … sickle-cell anemia and sickle-cell …

… hemoglobin … hemoglobin and sickle-cell anemia hemoglobin. These results have aided in
the clarification of both the genetic and the clinical aspects of sickle-cell anemia and sickle-cell …

… In sickle cell anemia, HbS polymer is present at 70% O 2 … Patients with untreated sickle cell
anemia, sickle cell anemia … symptomatic; all have hemolytic anemia. The contrast between …