Articles with public access mandates - Susan KirkLearn more
Not available anywhere: 5
“I'm not what I used to be”: A qualitative study exploring how young people experience being diagnosed with a chronic illness
S Kirk, D Hinton
Child: care, health and development 45 (2), 216-226, 2019
Mandates: National Institute for Health Research, UK
Living with a powered wheelchair: exploring children’s and young people’s experiences
S Gudgeon, S Kirk
Disability and Rehabilitation: Assistive Technology 10 (2), 118-125, 2015
Mandates: National Institute for Health Research, UK
Parents' perspectives of cleft lip and/or palate services: A qualitative interview
PA Nelson, SA Kirk
The Cleft Palate-Craniofacial Journal 50 (3), 275-285, 2013
Mandates: UK Medical Research Council
Paediatric multiple sclerosis: a qualitative study of families’ diagnosis experiences
D Hinton, S Kirk
Archives of disease in childhood 100 (7), 623-629, 2015
Mandates: National Institute for Health Research, UK
Self-care of young people with long-term physical and mental health conditions
S Kirk, S Pryjmachuk
Nursing children and young people 28 (7), 2016
Mandates: US National Institutes of Health, National Institute for Health Research, UK
Available somewhere: 18
How a moderated online discussion forum facilitates support for young people with eating disorders
S Kendal, S Kirk, R Elvey, R Catchpole, S Pryjmachuk
Health Expectations 20 (1), 98-111, 2017
Mandates: National Institute for Health Research, UK
How do peers promote social inclusion of children with disabilities? A mixed-methods systematic review
RL Woodgate, M Gonzalez, L Demczuk, WM Snow, S Barriage, S Kirk
Disability and rehabilitation 42 (18), 2553-2579, 2020
Mandates: Canadian Institutes of Health Research
Asset-based community development: narratives, practice, and conditions of possibility—a qualitative study with community practitioners
R Harrison, C Blickem, J Lamb, S Kirk, I Vassilev
Sage Open 9 (1), 2158244018823081, 2019
Mandates: National Institute for Health Research, UK
An exploration of how young people and parents use online support in the context of living with cystic fibrosis
S Kirk, L Milnes
Health Expectations 19 (2), 309-321, 2016
Mandates: National Institute for Health Research, UK
Hidden caring, hidden carers? Exploring the experience of carers for people with long‐term conditions
S Knowles, R Combs, S Kirk, M Griffiths, N Patel, C Sanders
Health & social care in the community 24 (2), 203-213, 2016
Mandates: National Institute for Health Research, UK
Living with uncertainty and hope: A qualitative study exploring parents’ experiences of living with childhood multiple sclerosis
D Hinton, S Kirk
Chronic illness 13 (2), 88-99, 2017
Mandates: National Institute for Health Research, UK
Patient safety in marginalised groups: a narrative scoping review
S Cheraghi-Sohi, M Panagioti, G Daker-White, S Giles, L Riste, S Kirk, ...
International journal for equity in health 19, 1-26, 2020
Mandates: National Institute for Health Research, UK
Participation in voluntary and community organisations in the U nited K ingdom and the influences on the self‐management of long‐term conditions
M Jeffries, A Mathieson, A Kennedy, S Kirk, R Morris, C Blickem, ...
Health & social care in the community 23 (3), 252-261, 2015
Mandates: National Institute for Health Research, UK
Developing a model of mental health self-care support for children and young people through an integrated evaluation of available types of provision involving systematic review …
S Pryjmachuk, R Elvey, S Kirk, S Kendal, P Bower, R Catchpole
Mandates: National Institute for Health Research, UK
A Blueprint for Involvement: Reflections of lived experience co-researchers and academic researchers on working collaboratively
Blueprint Writing Collective claire. fraser@ manchester. ac. uk Fraser ...
Research involvement and engagement 8 (1), 68, 2022
Mandates: National Institute for Health Research, UK
Connecting local support: a qualitative study exploring the role of voluntary organisations in long-term condition management
R Morris, S Kirk, A Kennedy, I Vassilev, A Mathieson, M Jeffries, ...
Chronic illness 11 (2), 140-155, 2015
Mandates: National Institute for Health Research, UK
Self‐management interventions for children and young people with sickle cell disease: A systematic review
BA Poku, KM Atkin, S Kirk
Health Expectations 26 (2), 579-612, 2023
Mandates: US National Institutes of Health, National Institute for Health Research, UK
Respite care: qualitative arts-based findings on the perspectives and experiences of families of children and youth with special healthcare needs residing in Manitoba, Canada
RL Woodgate, C Isaak, A Kipling, S Kirk, K Keilty
BMJ open 13 (6), e073391, 2023
Mandates: Canadian Institutes of Health Research
How a child's gender mediates maternal care and expectations in the fatigue experiences of adolescents with sickle cell disease
BA Poku, A Pilnick, S Kirk
Journal of Family Studies 29 (4), 1606-1627, 2023
Mandates: UK Economic and Social Research Council
Perceptions of the key components of effective, acceptable and accessible services for children and young people experiencing common mental health problems: a qualitative study
S Kirk, C Fraser, N Evans, R Lane, J Crooks, G Naughton, S Pryjmachuk
BMC Health Services Research 23 (1), 391, 2023
Mandates: US National Institutes of Health, National Institute for Health Research, UK
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