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2005, Número 4

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Ann Hepatol 2005; 4 (4)


Liver dysfunction in steady state sickle cell disease

Kotila T, Adedapo K, Adedapo A, Oluwasola O, Fakunle E, Brown B

Idioma: Ingles.
Referencias bibliográficas: 15
Paginas: 261-263
Archivo PDF: 38.64 Kb.


FRAGMENTO

Sin resumen


REFERENCIAS (EN ESTE ARTÍCULO)

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  3. Ahn H, Li CS, Wang W. Sickle cell hepetopathy: clinical presentation, treatment, and outcome in paediatric and adult patients. Paediatr Blood Cancer 2005: 184-90

  4. Schubert TT. Hepatobiliary system in sickle cell disease. Gastroenterology 1986; 90: 2013-21.

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  7. Bauer TW, Moore GW, Hutchins GM. The liver in sickle cell disease: a clinicopathologic study of 70 patients. Am J Med 1980; 69: 833-837.

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  10. Khurshid I, Anderson L, Downie GH, Pape GS. Sickle cell disease, extreme hyperbilirubinaemia, and pericardial tamponade: case report and review of the literature. Crit Care Med 2002; 30: 2363-2367.

  11. Shao SH, Orringer EP. Sickle cell intrahepatic cholestasis: approach to a difficult problem. Am J Gastroenterol 1995; 90: 2048-2050.

  12. Soliman AT, Bererhi H, Darwish A, Alzalabani MM, Wali Y, Ansari B. Decreased bone mineral density in prepubertal children with sickle cell disease: correlation with growth parameters, degree of siderosis and secretion of growth factors. J Trop Pediatr 1998; 4: 194-8.

  13. Porter JB, Huchas ER. Transfusion and exchange transfusion in sickle cell anaemias, with particular reference to iron metabolism. Acta Haematol 1987; 78: 198-205.

  14. Fasola FA, Odaibo GN, Aken’Ova YA, Olaleye OD. Hepatitis B and C viral markers in patients with sickle cell disease in Ibadan, Nigeria. Afr. J Med Med Sci 2003; 32: 293-295.

  15. Allain JP, Daniel C, Soldan K, Sarkodie F, Phelps B, Giachetti C, Shyamala V, et al. The risk of hepatitis B virus infection by transfusion in Kumasi Ghana. Blood 2003; 101:2419-2425.




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