Subclinical ischaemic episodes during the steady state of sickle cell anaemia.

Author:

Akinola N O,Stevens S M,Franklin I M,Nash G B,Stuart J

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference24 articles.

1. Pain in sickle cell disease;Pearson, H.A.; Wethers, D.; Johnson, S.;N Engl J7 Med,1991

2. Fluctuating deformability of oxygenated sickle erythrocytes in the asymptomatic state and in painful crisis;Lucas, G.S.; Caldwell, N.M.; Stuart, J.;Br J Haematol,1985

3. Erythrocyte adherence to endothelium in sickle-cell anemia. A possible determinant of disease severity;Hebbel, R.P.; Boogaerts, M.A.B.; Eaton, J.W.; Steinberg, M.H.;N Engl JfMed,1980

4. Heterogeneity of red cells in the sickler: a characteristic with practical clinical and pathophysiological implications;Fabry, M.E.; Nagel, R.L.;Blood Cells,1982

5. The percentage of dense red cells does not predict incidence of sickle cell painful crisis;Billett, H.H.; Kim, K.; Fabry, M.E.; Nagel, R.L.;Blood,1986

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