Monitoring the acute phase response to vaso-occlusive crisis in sickle cell disease.

Author:

Stuart J,Stone P C,Akinola N O,Gallimore J R,Pepys M B

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference19 articles.

1. Painful crises in sickle cell diseasepatients';Murray, N.; May, A.;perspectives. BrMedJ,1988

2. Rheological changes in the prodromal and established phases of sickle cell vaso-occlusive crisis;Akinola, N.O.; Stevens, S.M.E.; Franklin, I.M.; Nash, G.B.; Stuart, J.;BrJ Haematol,1992

3. Subclinical ischaemic episodes during the steady state of sickle cell anaemia;Akinola, N.O.; Stevens, S.M.E.; Franklin, I.M.; Nash, G.B.; Stuart, J.;J Clin Pathol,1992

4. Is there an acute phase response in steady-state sickle cell disease?;Singhal, A.; Doherty, J.F.; Raynes, J.G.;Lancet,1993

5. Acute phase proteins with special reference to C-reactive protein and related proteins (pentaxins) and serum amyloid A protein;Pepys, M.B.; Baltz, M.L.;Adv Immunol,1983

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