WONKAM, Ambroise et al. The burden of sickle cell disease in Cape Town. SAMJ, S. Afr. med. j. [online].
2012,
vol.102, n.9, pp. 753-754.
ISSN 0256-9574.
|
|
2. Weatherall DJ. The inherited diseases of hemoglobin are an emerging global health burden. Blood 2010;115(22):4331-4336. [ Links ] 3. Malowany JI, Butany J. Pathology of sickle cell disease. Semin Diagn Pathol 2012;29(1):49-55. [ Links ] 4. Bartolucci P, Galactéros F. Clinical management of adult sickle-cell disease. Curr Opin Hematol 2012;19(3):149-155. [ Links ] 5. Platt OS, Brambilla DJ, Rosse WF, et al. Mortality in sickle cell disease: Life expectancy and risk factors for early death. N Engl J Med 1994;330:1639-1644. [ Links ] 6. Lanzkron S, Strouse JJ, Wilson R, et al. Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease. Ann Intern Med 2008;148(12):939-955. [ Links ] 7. Strouse JJ, Lanzkron S, Beach MC, et al. Hydroxyurea for sickle cell disease: a systematic review for efficacy and toxicity in children. Pediatrics 2008;122(6):1332-1342. [ Links ] 8. Bonafede RP, Botha MC, Beighton P. Inherited anaemias in the Greek community of Cape Town. J Med Genet 1979;16(3):197-200. [ Links ] 9. Bird AR, Ellis P, Wood K, Mathew C, Karabus C. Inherited haemoglobin variants in a South African population. J Med Genet 1987;24(4):215-219. [ Links ] 10. Bird AR, Karabus CD, Hartley PS. Microcytic anaemia and haemoglobinopathy in Cape Town children. S Afr Med J 1982;62(13):429-430. [ Links ] 11. Reddy MV, Ward FA .The sickle-cell phenomenon in South Africa. S Afr Med J 1969;43:1217-1219. [ Links ] 12. Dunston T, Rowland R, Huntsman RG, Yawson G Sickle-cell haemoglobin C disease and sickle-cell beta thalassemia in white South Africans. S Afr Med J 1972;46:1423-1426. [ Links ] 13. Beighton P, Botha MC.Inherited disorders in the black population of southern Africa. Part I. Historical and demographic background; genetic haematological conditions. S Afr Med J 1986;69(4):247-249. [ Links ] 14. Howard J, Davies SC. Sickle cell disease in Northern Europe. Scandinavian Journal of Clinical Laboratory Investigation 2007;67(1):27-38. [ Links ] 15. Labie D, Pagnier J, Lapoumeroulie C, et al. Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients. Proceedings of the National Academy of Sciences (PNAS) 1985;82:2111-2114. [ Links ] 16. Makani J, Menzel S, Nkya S, et al. Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia. Blood 2011;117(4):1390-1392. [ Links ] 17. Aygun B, Wruck LM, Schultz WH, et al. Chronic transfusion practices for prevention of primary stroke in children with sickle cell anemia and abnormal TCD velocities. Am J Hematol 2012;87(4):428-430. [ Links ] 18. Makani J, Cox SE, Soka D, et al. Mortality in sickle cell anaemia in Africa: A prospective cohort study in Tanzania. PLoS One 2011;6(2):e14699. [ Links ] 19. Aluoch J, Jacobs P. Sickle-cell disease in sub-Saharan Africa - past, present and future status. S Afr Med J 1996;86(8):982-983. [ Links ] |
