Now showing items 11-18 of 18
Midwives' and senior student midwives' knowledge of haemoglobinopathies in England.
Objective: To examine midwives' and senior student midwives' knowledge concerning sickle cell anaemia and beta-thalassaemia. Design: Survey using the Dyson Questionnaires. Setting: Study days on 26 sites across England ...
Midwives' knowledge of haemoglobinopathies
(Hayward Medical Communications, 1996)
This paper addresses the educational implications of a study of midwives and senior student midwives knowledge of haemoglobinopathies. Knowledge was assessed from 850 multiple choice questionnaires. Respondents who had ...
'Race', ethnicity and haemoglobin disorders
The new genetics has brought forth concerns that such developments as screening for genetic diseases will accentuate the oppression of minority ethnic groups [Bradby (1996) Genetics and racism. In The Troubled Helix: ...
Beta Thalassaemia: Current carrier and community awareness in Manchester.
(De Montfort University, 1994)
Thalassaemia major: Counselling and community education.
(Health Visitors Association, 1994-01)
In two previous articles, Simon Dyson, Verna Davis, and Raheya Rahman described the basic facts about thalassaemia and also considered the outcome of a preliminary survey establishing levels of awareness among community ...
Blood relations: educational implications of sickle cell anaemia and thalassaemia.
(Routledge/Open University Press, 1992)
Sickle cell anaemia and thalassaemia are genetic conditions which affect people from Black and ethnic minority communities in much greater numbers than White people, and they remain ill-understood. In this chapter Simon ...
Thalassaemia: Current community knowledge in Manchester.
(Health Visitors Association, 1993-12)
In this second of three articles Simon Dyson, Verna Davis and Rafeya Rahman describe a study carried out in Manchester for the sickle-cell anaemia and thalassaemia centre to gauge the extent of community awareness about ...
Haemoglobinopathies, antenatal screening and the midwife.
(Mark Allen, 1996)
Key Points Lack of national enforceable and funded standards for screening for the haemoglobinopathies means that a great deal of discretion is devolved to the individual midwife. Naive conceptions of ‘race’ and lack of ...