Adverse neurological outcomes in Nigerian children with sickle cell disease

Author:

Lagunju I. A.,Brown B. J.

Publisher

Springer Science and Business Media LLC

Subject

Hematology

Reference40 articles.

1. Ohene-Frempong K. Abnormalities of haemoglobin structure and function. Sickle Cell Disease. In: Rudolph CD, Rudolph AM, Hostetter MK, Lister G, Siegel NJ, editors. Rudolph pediatrics. New York: McGraw Hill Medical Publishing Division, 2003. p. 1534–40.

2. Saunthararajah Y, Vichinsky EP, Embury SH. Sickle cell disease. In: Hoffman R, Benz EJ, Shattil SJ, et al., editors. Haematology basic principles and practice. Philadelphia: Elsevier; 2005. p. 605–43.

3. Serjeant GR. Sickle cell disease. Oxford: Oxford University Press; 1985. p. 1–12.

4. Hebbel RP, Boogaertes MAB, Eaton JN, Steinberg MH. Erythrocyte adherence to endothelium in sickle cell anaemia; a possible determinant of disease severity. N Engl J Med. 1980;302:992–5.

5. Elion J, Laurance S, Lapoumeroulie C. Pathophysiology of sickle cell disease. Med Trop (Mars). 2010;70:454–8.

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