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Sickle Cell Anemia Evolution

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... asked about drug use and whether they have sickle-cell anemia (Barker, 2001). genetic vulnerabilities to certain illnesses (such as, for instance, sickle cell anemia) as well as possible treatments (2) PBS. "Human Evolution." Evolution. (2) PBS. "Human Evolution." Evolution. <http://www.pbs.org/wgbh/evo lution/library/07/index.html> itself. It is evolution that moves the story forward and evolution that brings it to an ending that is, like evolution, basis of ethnicity include Tay-Sachs and Canavan diseases, thalassemias, and sickle cell anemia. The most common ...



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Sources list for SICKLE CELL ANEMIA EVOLUTION:

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

Nia J, Lam WC, Kleinman DM, Kirby M, Liu ES, Eng KT. Retinopathy in sickle cell trait: does it exist? Can J Ophthalmol 2003;38:46-51.
Sickle Cell Retinopathy

 


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