Prevention practices influencing frequency of occurrence of vaso-occlusive crisis among sickle cell patients in Abeokuta South Local Government Area of Ogun State, Nigeria

Author:

Amoran Olorunfemi Emmanuel,Jimoh Ahmed Babatunde,Ojo Omotola,Kuponiyi Temitope

Publisher

Springer Science and Business Media LLC

Subject

Hematology,Molecular Biology

Reference23 articles.

1. World Health Organization. Sickle Cell Anaemia Report by the Secretariat.Fifty ninth World Health Assembly [homepage on the internet]. C2006. 2011. Avaible from http://www.afro.who.int/en/nigeria/nigeria-publications/1775-sickle%20cell%20disease.html .

2. Diallo D, Tchernia G. Sickle cell in Africa. Currie Opine Hematol. 2002;9(2):111–6. doi: 10.1097/00062752-200203000-0005 .

3. Schatz J, McClellan CB. Sickle cell disease as a neurodevelopmental disorder. Ment Retard Dev Disabil Res Rev. 2006;12:200–7. doi: 10.1002/mrdd.20115 .

4. Shapiro BS. Management of painful episodes in sickle cell disease. In: Schechter NL, Berde CB, Yaster M, editors. Pain in Infants, Children and Adolescents. Baltimore: Williams and Wikins; 1993.

5. Midence K, Shand P. Family and social issues in sickle cell disease. Health Visit. 1992;65:441–3.

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