Now showing items 1-10 of 28
Lessons for intermediate and low prevalence areas in England from the Ethnicity Questions and Antenatal Screening for sickle cell / thalassaemia [EQUANS] study
This study evaluates a temporary research-based intervention of universal ante-natal screening for sickle cell/thalassaemia in two areas of England of intermediate (1.29 per 10,000) and low (0.18 per 10,0000) expected ...
Sickle cell anaemia and deaths in custody in the UK and USA
An unexplained death in custody represents an important focal point for public scrutiny of the criminal justice system, especially when excess deaths occur in those of minority ethnic descent. Sickle cell anaemia is a ...
Sickle cell and deaths in custody
(Whiting & Birch, 2009)
Healthcare provision for sickle cell disease in Ghana: challenges for the African context
Sickle cell disease (SCD) is an inherited disorder affecting 2% of all babies born in Ghana. SCD is the commonest genetic condition of clinical and epidemiological importance in Africa, and over 95% of children born with ...
The health status of minority ethnic groups.
Sickle cell: a signifier for the New Europe.
(Trentham Books, 2009)
Sickle cell and thalassaemia are health issues affecting many established and migrant minority ethnic groups across Europe. This book chapter seeks to demonstrate that sickle cell as an issue signifies both the challenges, ...
Working with sickle cell / thalassaemia support groups
(Jessica Kingsley, 2000)
This chapter reports on the processes of research in working with support groups for sickle cell anaemia and beta-thalassaemia in conducting community-based surveys of knowledge of these two inherited conditions. The ...
Ethnic question and antenatal screening for sickle cell / thalassaemia (EQUANS) in England
(Athens Institute for Education and Research, 2005)
Ethnicity and screening for sickle cell/ thalassaemia
(Oxford: Elsevier Churchill Livingstone, 2005)
Genetic traits as pollution: ‘White English’ carriers of sickle cell or thalassaemia
From April 2004, the policy for neonatal screening for sickle cell in England has been to base the screening on universal principles (offer the screening to all new-born babies) rather than selective screening (an attempt ...