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Sickel Cell Anemia

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... performance, through, for instance, verbally reacting aloud as one might in the African-American church tradition, or of knowing what is `supposed' to happen along with the actors, as an audience watching a familiar folktale in the Noh to the ideological power struggles of the various characters. The mixed, intercultural audience therefore has, as such, as frail and often incompetent and highly emotional. However, these stereotypes are changing and developing a alter-ego tradition. The play itself takes place over a single day in 1927, in a Chicago recording studio. The great blues singer Ma Rainey ...



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Sources list for SICKEL CELL ANEMIA:

Charache, et. al. 1995. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. N Engl J Med 332:1317-22.
Sickle Cell Disease

Powars, D, et al. 1993. Sickle cell anemia. Beta s gene cluster haplotypes as genetic markers for severe disease expression. Am. J. Dis. Child. 147:1197-1202.
Sickle Cell Disease

Seltzer, WK; Abshire, TC; Lane, PA; Roloff, JS; Githens, JH. 1992. Molecular genetic studies in black families with sickle cell anemia and unusually high levels of fetal hemoglobin. Hemoglobin 16: 363-77.
Sickle Cell Disease

Powars, D, et. al. 1994. Beta-S gene cluster haplotypes modulate hematologic and hemorheologic expression in sickle cell anemia. Use in predicting clinical severity. Am. J. Ped. Hematology-Oncology 16:55-61.
Sickle Cell Disease

NIH. "What Are the Unique Properties of All Stem Cells?" Stem Cell Basics. Stem Cell Information. National Institute of Health. 2004. http://stemcells.nih.gov/info/basics/basics2.asp
Stem Cell Research

 

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