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Karen Lowton

Showing results (1-10 of 42) with videos related to

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Social Science & Medicine (1982)|February 26, 2003
'Double or quits': perceptions and management of organ transplantation by adults with cystic fibrosisKaren Lowton
Social Science & Medicine (1982)|August 21, 2009
'A bed in the middle of nowhere': parents' meanings of place of death for adults with cystic fibrosisKaren Lowton
Journal of Advanced Nursing|July 9, 2002
Parents and partners: lay carers' perceptions of their role in the treatment and care of adults with cystic fibrosisKaren Lowton
Sociology of Health & Illness|May 13, 2024
Multimorbidity: Inequalities, lived experience and the need for service redesignKaren Lowton
Sociology of Health & Illness|July 13, 2021
Understanding advances in treatment and care of people living with and alongside HIV: Contributions from the Sociology of Health and IllnessKaren Lowton
Qualitative Health Research|February 11, 2004
Only when I cough? Adults' disclosure of cystic fibrosisKaren Lowton
Social Science & Medicine (1982)|May 26, 2005
Trials and tribulations: understanding motivations for clinical research participation amongst adults with cystic fibrosisKaren Lowton
Health & Social Care in the Community|July 30, 2009
What is the perceived nature of parental care and support for young people with cystic fibrosis as they enter adult health services?Nicola Iles, Karen Lowton
Sociology of Health & Illness|April 19, 2020
Academic developments and publishing changes - an update from the editorsKaren Lowton, Flis Henwood
Sociology of Health & Illness|September 8, 2022
The effects of disappearing social safety nets on inequalities in healthKaren Lowton, Flis Henwood
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
Social Science & Medicine (1982)|February 26, 2003
'Double or quits': perceptions and management of organ transplantation by adults with cystic fibrosisKaren Lowton
Social Science & Medicine (1982)|August 21, 2009
'A bed in the middle of nowhere': parents' meanings of place of death for adults with cystic fibrosisKaren Lowton
Journal of Advanced Nursing|July 9, 2002
Parents and partners: lay carers' perceptions of their role in the treatment and care of adults with cystic fibrosisKaren Lowton
Sociology of Health & Illness|May 13, 2024
Multimorbidity: Inequalities, lived experience and the need for service redesignKaren Lowton
Sociology of Health & Illness|July 13, 2021
Understanding advances in treatment and care of people living with and alongside HIV: Contributions from the Sociology of Health and IllnessKaren Lowton
Qualitative Health Research|February 11, 2004
Only when I cough? Adults' disclosure of cystic fibrosisKaren Lowton
Social Science & Medicine (1982)|May 26, 2005
Trials and tribulations: understanding motivations for clinical research participation amongst adults with cystic fibrosisKaren Lowton
Health & Social Care in the Community|July 30, 2009
What is the perceived nature of parental care and support for young people with cystic fibrosis as they enter adult health services?Nicola Iles, Karen Lowton
Sociology of Health & Illness|April 19, 2020
Academic developments and publishing changes - an update from the editorsKaren Lowton, Flis Henwood
Sociology of Health & Illness|September 8, 2022
The effects of disappearing social safety nets on inequalities in healthKaren Lowton, Flis Henwood
Pageof 5