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Geraldine Foley
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Using grounded theory method to capture and analyze health care experiences
G Foley, V Timonen
Health services research 50 (4), 1195-1210, 2015
5982015
Using grounded theory method to capture and analyze health care experiences
G Foley, V Timonen
Health services research 50 (4), 1195-1210, 2015
5982015
Challenges when using grounded theory: A pragmatic introduction to doing GT research
V Timonen, G Foley, C Conlon
International journal of qualitative methods 17 (1), 1609406918758086, 2018
5812018
Confused about theoretical sampling? Engaging theoretical sampling in diverse grounded theory studies
C Conlon, V Timonen, C Elliott-O’Dare, S O’Keeffe, G Foley
Qualitative health research 30 (6), 947-959, 2020
2212020
Amyotrophic lateral sclerosis: improving care with a multidisciplinary approach
A Hogden, G Foley, RD Henderson, N James, SM Aoun
Journal of multidisciplinary healthcare, 205-215, 2017
1622017
Interviewing as a vehicle for theoretical sampling in grounded theory
G Foley, V Timonen, C Conlon, CE O’Dare
International Journal of Qualitative Methods 20, 1609406920980957, 2021
1152021
Exerting control and adapting to loss in amyotrophic lateral sclerosis
G Foley, V Timonen, O Hardiman
Social Science & Medicine 101, 113-119, 2014
1012014
Perceptions of quality of life in people with ALS: effects of coping and health care
G Foley, P O'Mahony, O Hardiman
Amyotrophic lateral sclerosis 8 (3), 164-169, 2007
902007
Patients’ perceptions of services and preferences for care in amyotrophic lateral sclerosis: a review
G Foley, V Timonen, O Hardiman
Amyotrophic Lateral Sclerosis 13 (1), 11-24, 2012
762012
Acceptance and decision making in amyotrophic lateral sclerosis from a life-course perspective
G Foley, V Timonen, O Hardiman
Qualitative health research 24 (1), 67-77, 2014
702014
“I hate being a burden”: the patient perspective on carer burden in amyotrophic lateral sclerosis
G Foley, V Timonen, O Hardiman
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 17 (5-6), 351-357, 2016
502016
Understanding psycho-social processes underpinning engagement with services in motor neurone disease: a qualitative study
G Foley, V Timonen, O Hardiman
Palliative Medicine 28 (4), 318-325, 2014
492014
Video-based online interviews for palliative care research: A new normal in COVID-19?
G Foley
Palliative Medicine 35 (3), 625-626, 2021
462021
Experience of services as a key outcome in amyotrophic lateral sclerosis (ALS) care: the case for a better understanding of patient experiences
G Foley, V Timonen, O Hardiman
American Journal of Hospice and Palliative Medicine® 29 (5), 362-367, 2012
382012
Experience of services as a key outcome in amyotrophic lateral sclerosis (ALS) care: the case for a better understanding of patient experiences
G Foley, V Timonen, O Hardiman
American Journal of Hospice and Palliative Medicine® 29 (5), 362-367, 2012
382012
Mutual support between patients and family caregivers in palliative care: a systematic review and narrative synthesis
R McCauley, R McQuillan, K Ryan, G Foley
Palliative Medicine 35 (5), 875-885, 2021
342021
Decision-making among patients and their family in ALS care: a review
G Foley, G Hynes
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 19 (3-4), 173-193, 2018
302018
Decision-making in palliative care: patient and family caregiver concordance and discordance—systematic review and narrative synthesis
SM Symmons, K Ryan, SM Aoun, LE Selman, AN Davies, N Cornally, ...
BMJ supportive & palliative care 13 (4), 374-385, 2023
252023
The complexity of care in amyotrophic lateral sclerosis
G Foley
Amyotrophic Lateral Sclerosis 12 (3), 160, 2011
152011
The supportive relationship between palliative patients and family caregivers
G Foley
BMJ Supportive & Palliative Care 8 (2), 184-186, 2018
132018
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