A. Hillman

发表

Power, agency and participatory agendas: A critical exploration of young people’s engagement in participative qualitative research

Nicola J. Ross, E. Renold, S. Holland, 2010 .

Moving stories: using mobile methods to explore the everyday lives of young people in public care

Nicola J. Ross, E. Renold, S. Holland, 2009 .

Right place ‐ wrong person: dignity in the acute care of older people

M. Calnan, A. Hillman, W. Tadd, 2011 .

Protocol for the IDEAL-2 longitudinal study: following the experiences of people with dementia and their primary carers to understand what contributes to living well with dementia and enhances active life

Roy W Jones, J. Rusted, Yu-Tzu Wu, 2018, BMC Public Health.

An evaluation of a vocational group for people with mental health problems based on The WORKS framework

E. Fossey, Danielle Hitch, A. Hillman, 2017 .

‘We're happy as we are’: the experience of living with possible undiagnosed dementia

Catherine A. Macleod, L. Clare, B. Woods, 2021, Ageing and Society.

Impact of COVID-19 on 'Living Well' with Mild-to-Moderate Dementia in the Community: Findings from the IDEAL Cohort.

F. Matthews, C. Victor, L. Clare, 2021, Journal of Alzheimer's disease : JAD.

Managing the medical-industrial complex.

D. Nash, W. Kissick, A. Hillman, 1986, The New England journal of medicine.

Cultural representations of dementia

A. Hillman, J. Latimer, 2017, PLoS medicine.

‘I often worry about the older person being in that system’: exploring the key influences on the provision of dignified care for older people in acute hospitals

A. Bayer, A. Hillman, W. Tadd, 2012, Ageing and Society.

A Comprehensive Model of Factors Associated With Capability to “Live Well” for Family Caregivers of People Living With Mild-to-Moderate Dementia

Roy W Jones, J. Rusted, I. Rippon, 2018, Alzheimer disease and associated disorders.

A Comprehensive Model of Factors Associated With Subjective Perceptions of “Living Well” With Dementia

Roy W Jones, J. Rusted, I. Rippon, 2018, Alzheimer's & Dementia.

The everyday lives of children in care: using a sociological perspective to inform social work practice

Nicola J. Ross, E. Renold, S. Holland, 2008 .

Dignity in Practice: An exploration of the care of older adults in acute NHS Trusts

M. Calnan, A. Hillman, W. Tadd, 2011 .

From Right Place - Wrong Person, to Right Place - Right Person: Dignified Care for Older People

M. Calnan, A. Bayer, A. Hillman, 2012, Journal of health services research & policy.

Risk, governance and the experience of care

M. Calnan, A. Bayer, A. Hillman, 2013, Sociology of health & illness.

`Becoming Participant'

Alexandra Hillman, Emma Renold, Nicola J. Ross, 2008 .

Dualities of dementia illness narratives and their role in a narrative economy

L. Clare, I. Jones, A. Hillman, 2018, Sociology of health & illness.

Effects of social restrictions on people with dementia and carers during the pre‐vaccine phase of the COVID‐19 pandemic: Experiences of IDEAL cohort participants

C. Victor, L. Clare, S. Stapley, 2022, Health & social care in the community.

PaCTS 1.0: A Crowdsourced Reporting Standard for Paleoclimate Data

Yolanda Gil, Varun Ratnakar, Daniel Garijo, 2019, Paleoceanography and Paleoclimatology.

Diagnosing dementia: Ethnography, interactional ethics and everyday moral reasoning

A. Hillman, 2016, Social theory & health : STH.

Fear and anxiety: Affects, emotions and care practices in the memory clinic

A. Hillman, Julia Swallow, 2018, Social studies of science.

Rights, ‘right on’ or the right thing to do? A critical exploration of young people's engagement in participative social work research

Nicola J. Ross, E. Renold, S. Holland, 2008 .

Living with dementia during the COVID-19 pandemic: coping and support needs of community dwelling people with dementia and their family carers. : Research findings from the IDEAL COVID-19 Dementia Initiative (IDEAL-CDI)

C. Victor, L. Clare, C. Pentecost, 2021 .

Living with dementia under COVID-19 restrictions: coping and support needs among people with dementia and carers from the IDEAL cohort

C. Victor, L. Clare, A. Hillman, 2021, Ageing and Society.

Impact of COVID-19 on ‘living well’ with mild-to- moderate dementia in the community: ndings from the IDEAL cohort

F. Matthews, C. Victor, L. Clare, 2021 .

Biomarkers and brains: situating dementia in the laboratory and in the memory clinic

A. Hillman, J. Latimer, 2019, New genetics and society.

Pathways and prospects in cancer research: Securing futures and negotiating boundaries

G. Elwyn, A. Hillman, Jamie Lewis, 2017 .

Pathways and prospects in cancer research: Securing futures and negotiating boundaries

G. Elwyn, A. Hillman, Jamie Lewis, 2017, BioSocieties.

‘All the world’s a stage’: Accounting for the dementia experience – insights from the IDEAL study

L. Clare, Ruth A. Lamont, I. Jones, 2020 .

‘Why must I wait?’ The performance of legitimacy in a hospital emergency department

A. Hillman, 2013, Sociology of health & illness.

Negotiating access : Practices of inclusion and exclusion in the performance of 'real' emergency medicine.

A. Hillman, 2007 .

The precariousness of living with, and caring for people with, dementia: Insights from the IDEAL programme.

A. Hillman, C. Quinn, C. Pentecost, 2023, Social science & medicine.

Fear and anxiety: Affects, emotions and care practices in the memory clinic

A. Hillman, Julia Swallow, 2018, Social Studies of Science.

A comprehensive model of factors associated with capability to “live well” for family caregivers of people living with mild tomoderate dementia

J. Rusted, I. Rippon, Yu-Tzu Wu, 2019 .

Somaticization, the making and unmaking of minded persons and the fabrication of dementia

A. Hillman, J. Latimer, 2019, Social studies of science.

Ordering, Enrolling, and Dismissing

A. Hillman, J. Latimer, P. White, 2012 .

Institutions of care, moral proximity and demoralisation: The case of the emergency department

A. Hillman, 2015, Social Theory & Health.

‘Why must I wait?’ The performance of legitimacy in a hospital emergency department

A. Hillman, 2013, Sociology of health & illness.

Moving stories: using mobile methods to explore the everyday lives of young people in public care

Nicola J. Ross, E. Renold, S. Holland, 2009 .