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Paper On Sickle Cells

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... Women at risk for transmitting genetic disorders (eg, sickle cell disease, Tay-Sachs disease, cystic fibrosis) should be genetic vulnerabilities to certain illnesses (such as, for instance, sickle cell anemia) as well as possible treatments well. Even areas such as orthopedics, GI, urology, psychiatry, emergency services, neurology, general medicine, sickle Michigan. While a pediatric resident, Dr. Perricone researched sickle cell anemia using glycolic acid as a therapeutic more frequent than single-gene disorders. The relatively high frequency of some single-gene disorders, such as sickle ...



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Sources list for PAPER ON SICKLE CELLS:

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

Bailey, K; Morris, JS; Thomas, P; Serjeant, GR. 1992. Fetal hemoglobin and early manifestations of homozygous sickle cell disease. Arch. Dis. Child. 67:517-20.
Sickle Cell Disease

Kehinde MO, Akinsola FB. Ocular findings in sickle cell disease patients in lagos. Niger Postgrad Med J 2004;11:203-6.
Sickle Cell Retinopathy

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

Fany A, Boni S, Adjorlolo C, et al. [Retinopathy as a sickle-cell trait: myth or reality?]. J Fr Ophtalmol 2004;27:1025-30.
Sickle Cell Retinopathy

 

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