Hepatic sequestration in sickle cell anaemia.

Author:

Hatton C S,Bunch C,Weatherall D J

Publisher

BMJ

Subject

General Earth and Planetary Sciences,General Environmental Science,General Engineering

Reference7 articles.

1. Outbreak of aplastic crises in sickle cell anaemia associated with parvovirus-like agent;Serjeant, G.R.; Topley, J.M.; Mason, K.;Lancet,1981

2. Early deaths in Jamaican children with sickle cell disease;Rogers, D.W.; Clarke, J.M.; Cupidore, L.; Ramlal, A.M.; Sparke, B.R.; Serjeant, G.R.;Br Med J,1978

3. Acute chest syndrome in sickle cell disease;Davies, S.C.; Luie, P.J.; Win, A.A.; Riordan, J.F.; Brozovic, M.;Lancet,1984

4. Sickle cell anaemia. Clinical study of 54 cases;Henderson, A.B.;Am j Med,1950

5. The liver in sickle cell anemia;Green, T.W.; Conley, C.L.; Berthrong, M.;Bulletin of the Johns Hopkins Hospital,1953

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1. Hemoglobin scavenger receptor CD163 as a potential biomarker of hemolysis-induced hepatobiliary injury in sickle cell disease;American Journal of Physiology-Cell Physiology;2024-08-01

2. Liver in Systemic Disease;MacSween's Pathology of the Liver;2024

3. Molecular mechanisms of hepatic dysfunction in sickle cell disease: lessons from Townes mouse model;American Journal of Physiology-Cell Physiology;2022-08-01

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5. Clinical management of sickle cell liver disease in children and young adults;Archives of Disease in Childhood;2020-11-11

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