Sickle-cell disease in sub-Saharan Africa
Author:
Affiliation:
1. Faculty of Medicine & Biomedical Sciences; University of Yaoundé I; Yaoundé Cameroon
2. Yaoundé University Teaching Hospital; Yaoundé Cameroon
3. Yaoundé Central Hospital; Yaoundé Cameroon
Publisher
Wiley
Subject
Computer Networks and Communications,Hardware and Architecture,Software
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/voxs.12226/fullpdf
Reference87 articles.
1. A specific chemical difference between the globins of normal human and sickle-cell anaemia haemoglobin;Ingram;Nature,1956
2. Sickle Cell Disease: new Opportunities and Challenges in Africa;Makani;Scientific World Journal,2013
3. Global epidemiology of sickle haemoglobin in neonates: a contemporary geostatistical model-based map and population estimates;Piel;Lancet,2013
4. Global burden of sickle cell anaemia in children under five, 2010-2050: modelling based on demographics, excess mortality, and interventions;Piel;PLoS Med,2013
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3. Views and Experiences of Parents and Physicians on the Care Provided to Children with Sickle Cell Disease in Cameroon;2020-03-03
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