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Crispin Jenkinson

Showing results (71-80 of 144) with videos related to

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Journal of Health Services Research & Policy|June 25, 2003
Factors relating to patients' reports about hospital care for coronary heart disease in EnglandCrispin Jenkinson, Angela Coulter, Steve Bruster, et al.
Human Reproduction (Oxford, England)|July 6, 2006
Measuring quality of life in women with endometriosis: tests of data quality, score reliability, response rate and scaling assumptions of the Endometriosis Health Profile QuestionnaireGeorgina Jones, Crispin Jenkinson, Nicola Taylor, et al.
Journal of Parkinson'S Disease|March 28, 2014
An electronic version of the PDQ-39: acceptability to respondents and assessment of alternative response formatsDavid Morley, Sarah Dummett, Laura Kelly, et al.
Patient Related Outcome Measures|July 28, 2015
The Outcomes and Experiences Questionnaire: development and validationElizabeth Gibbons, Paul Hewitson, David Morley, et al.
Health and Quality of Life Outcomes|January 24, 2015
Evaluating the psychometric properties of an e-based version of the 39-item Parkinson's Disease QuestionnaireDavid Morley, Sarah Dummett, Laura Kelly, et al.
Health and Quality of Life Outcomes|June 27, 2013
Carer quality of life and experiences of health services: a cross-sectional survey across three neurological conditionsMichele Peters, Crispin Jenkinson, Helen Doll, et al.
Journal of Patient-Reported Outcomes|November 7, 2020
Development of a patient-reported outcome measure (PROM) and change measure for use in early recovery following hip or knee replacementLouise H Strickland, David W Murray, Hemant G Pandit, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 2, 2012
The impact of perceived lack of support provided by health and social care services to caregivers of people with motor neuron diseaseMichele Peters, Ray Fitzpatrick, Helen Doll, et al.
Journal of Health Services Research & Policy|February 9, 2013
Patients' experiences of health and social care in long-term neurological conditions in England: a cross-sectional surveyMichele Peters, Ray Fitzpatrick, Helen Doll, et al.
BMJ (Clinical Research Ed.)|January 20, 2010
The routine use of patient reported outcome measures in healthcare settingsJill Dawson, Helen Doll, Ray Fitzpatrick, et al.
Pageof 15

Showing results (71-80 of 144) with videos related to

Sort By:
Pageof 15
Journal of Health Services Research & Policy|June 25, 2003
Factors relating to patients' reports about hospital care for coronary heart disease in EnglandCrispin Jenkinson, Angela Coulter, Steve Bruster, et al.
Human Reproduction (Oxford, England)|July 6, 2006
Measuring quality of life in women with endometriosis: tests of data quality, score reliability, response rate and scaling assumptions of the Endometriosis Health Profile QuestionnaireGeorgina Jones, Crispin Jenkinson, Nicola Taylor, et al.
Journal of Parkinson'S Disease|March 28, 2014
An electronic version of the PDQ-39: acceptability to respondents and assessment of alternative response formatsDavid Morley, Sarah Dummett, Laura Kelly, et al.
Patient Related Outcome Measures|July 28, 2015
The Outcomes and Experiences Questionnaire: development and validationElizabeth Gibbons, Paul Hewitson, David Morley, et al.
Health and Quality of Life Outcomes|January 24, 2015
Evaluating the psychometric properties of an e-based version of the 39-item Parkinson's Disease QuestionnaireDavid Morley, Sarah Dummett, Laura Kelly, et al.
Health and Quality of Life Outcomes|June 27, 2013
Carer quality of life and experiences of health services: a cross-sectional survey across three neurological conditionsMichele Peters, Crispin Jenkinson, Helen Doll, et al.
Journal of Patient-Reported Outcomes|November 7, 2020
Development of a patient-reported outcome measure (PROM) and change measure for use in early recovery following hip or knee replacementLouise H Strickland, David W Murray, Hemant G Pandit, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 2, 2012
The impact of perceived lack of support provided by health and social care services to caregivers of people with motor neuron diseaseMichele Peters, Ray Fitzpatrick, Helen Doll, et al.
Journal of Health Services Research & Policy|February 9, 2013
Patients' experiences of health and social care in long-term neurological conditions in England: a cross-sectional surveyMichele Peters, Ray Fitzpatrick, Helen Doll, et al.
BMJ (Clinical Research Ed.)|January 20, 2010
The routine use of patient reported outcome measures in healthcare settingsJill Dawson, Helen Doll, Ray Fitzpatrick, et al.
Pageof 15