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On the possibility of a disabled life in capitalist ruins: Black workers with sickle cell disorder in England

Social science & medicine (1982), 2021-03, Vol.272, p.113713-113713, Article 113713

2021

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Extending specialist palliative care to people with heart failure: Semantic, historical and practical limitations to policy guidelines

Social science & medicine (1982), 2009-07, Vol.69 (2), p.147-153

2009

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Incidental Findings of Sickle Cell Trait From an Everyday Diabetes Test: Should General Health Care Providers and Testing Centers Report, Retest, or Refer?

Clinical diabetes, 2020-01, Vol.38 (1), p.101-107

2020

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An idealist vision of specialist palliative care: A response to the commentary by Selman, Beattie, Murtagh and Higginson

Social science & medicine (1982), 2009-07, Vol.69 (2), p.158-159

2009

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Self-Management of Chronic Pain: The Role of Religious Faith

Journal of disability & religion, 2016-10, Vol.20 (4), p.291-306

2016

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The associations among childhood trauma, loneliness, mental health symptoms, and indicators of social exclusion in adulthood: A UK Biobank study

Brain and behavior, 2023-04, Vol.13 (4), p.e2959-n/a

2023

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Unintended Consequences of Code Status in the Intensive Care Unit: What Happens After a Do-Not-Resuscitate Order Is Placed? A Retrospective Cohort Study

Journal of palliative medicine, 2024-04, Vol.27 (4), p.508

2024

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Why ethnic minority groups are under-represented in clinical trials: a review of the literature

Health & social care in the community, 2004-09, Vol.12 (5), p.382-388

2004

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'Talk to Me. There's Two of US': Fathers and Sickle Cell Screening

Sociology (Oxford), 2016-02, Vol.50 (1), p.178-194

2016

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Resignifying the sickle cell gene: Narratives of genetic risk, impairment and repair

Health (London, England : 1997), 2017-03, Vol.21 (2), p.171-188

2017

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Supporting children and young people when making decisions about joining clinical trials: qualitative study to inform multimedia website development

BMJ open, 2019-01, Vol.9 (1), p.e023984-e023984

2019

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Causal attributions, lifestyle change, and coronary heart disease: Illness beliefs of patients of South Asian and European origin living in the United Kingdom

Heart & lung, 2008-03, Vol.37 (2), p.91-104

2008

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Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome

Science (American Association for the Advancement of Science), 1990-06, Vol.248 (4960), p.1224-1227

1990

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South Asian participation in clinical trials: The views of lay people and health professionals

Health policy (Amsterdam), 2006-07, Vol.77 (2), p.149-165

2006

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Narrative as re-fusion: Making sense and value from sickle cell and thalassaemia trait

Health (London, England : 1997), 2016-11, Vol.20 (6), p.616-634

2016

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Representation of South Asian people in randomised clinical trials: analysis of trials' data

BMJ (Online), 2003-06, Vol.326 (7401), p.1244-1245

International edition, 2003

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Offering antenatal sickle cell and thalassaemia screening to pregnant women in primary care: a qualitative study of GPs' experiences

British journal of general practice, 2010-11, Vol.60 (580), p.822-828

2010

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Sickle cell and thalassaemia: global public health issues come of age

Ethnicity & health, 2011-08, Vol.16 (4-5), p.299-311

2011

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Decision-Making and Ante-Natal Screening for Sickle Cell and Thalassaemia Disorders: To What Extent do Faith and Religious Identity Mediate Choice?

Current sociology, 2008-01, Vol.56 (1), p.77-98

2008

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Offering antenatal sickle cell and thalassaemia screening to pregnant women in primary care: a qualitative study of women's experiences and expectations of participation

Health expectations : an international journal of public participation in health care and health policy, 2012-06, Vol.15 (2), p.115-125

2012

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Sickle cell, habitual dys‐positions and fragile dispositions: young people with sickle cell at school

Sociology of health & illness, 2011-03, Vol.33 (3), p.465-483

2011

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High mutation detection rate in the COL4A5 collagen gene in suspected Alport syndrome using PCR and direct DNA sequencing

Journal of the American Society of Nephrology, 1998-12, Vol.9 (12), p.2291-2301

1998

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Genetics and Global Public Health: Sickle Cell and Thalassaemia

1, 2012

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Laying foundations for health: food provision for under 5s in day care

Appetite, 2005-04, Vol.44 (2), p.207-213

2005

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Maximising recruitment and retention of general practices in clinical trials: a case study

British journal of general practice, 2008-11, Vol.58 (556), p.759-766

2008

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On the possibility of a disabled life in capitalist ruins: Black workers with sickle cell disorder in England

Extending specialist palliative care to people with heart failure: Semantic, historical and practical limitations to policy guidelines

Incidental Findings of Sickle Cell Trait From an Everyday Diabetes Test: Should General Health Care Providers and Testing Centers Report, Retest, or Refer?

An idealist vision of specialist palliative care: A response to the commentary by Selman, Beattie, Murtagh and Higginson

Self-Management of Chronic Pain: The Role of Religious Faith

The associations among childhood trauma, loneliness, mental health symptoms, and indicators of social exclusion in adulthood: A UK Biobank study

Unintended Consequences of Code Status in the Intensive Care Unit: What Happens After a Do-Not-Resuscitate Order Is Placed? A Retrospective Cohort Study

Why ethnic minority groups are under-represented in clinical trials: a review of the literature

'Talk to Me. There's Two of US': Fathers and Sickle Cell Screening

Resignifying the sickle cell gene: Narratives of genetic risk, impairment and repair

Supporting children and young people when making decisions about joining clinical trials: qualitative study to inform multimedia website development

Causal attributions, lifestyle change, and coronary heart disease: Illness beliefs of patients of South Asian and European origin living in the United Kingdom

Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome

South Asian participation in clinical trials: The views of lay people and health professionals

Narrative as re-fusion: Making sense and value from sickle cell and thalassaemia trait

Representation of South Asian people in randomised clinical trials: analysis of trials' data

Offering antenatal sickle cell and thalassaemia screening to pregnant women in primary care: a qualitative study of GPs' experiences

Sickle cell and thalassaemia: global public health issues come of age

Decision-Making and Ante-Natal Screening for Sickle Cell and Thalassaemia Disorders: To What Extent do Faith and Religious Identity Mediate Choice?

Offering antenatal sickle cell and thalassaemia screening to pregnant women in primary care: a qualitative study of women's experiences and expectations of participation

Sickle cell, habitual dys‐positions and fragile dispositions: young people with sickle cell at school

High mutation detection rate in the COL4A5 collagen gene in suspected Alport syndrome using PCR and direct DNA sequencing

Genetics and Global Public Health: Sickle Cell and Thalassaemia

Laying foundations for health: food provision for under 5s in day care

Maximising recruitment and retention of general practices in clinical trials: a case study

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