David Morley

• Pretesting an e-based version of the Oxford Participation and Activities Questionnaire (Ox-PAQ)

  Kelly L. et al, (2016), Value in Health, 19, A485 - A485

• Use of the Routine Activities Domain of the Oxford Participation & Activities Questionnaire (Ox-PAQ)

  Kelly L. et al, (2016), Quality of Life Research, 25, 106 - 106

• Underinvestigated parental conditions: an overview

  Kelly L. and Morley DP., (2016), Children’s and young people’s response to parental illness, 153 - 170

• Parental Parkinson’s disease

  Morley DP. and Book E., (2016), Children’s and young people’s response to parental illness, 23 - 36

• Measuring the impact of parental illness

  Kelly L. et al, (2016), Children’s and young people’s response to parental illness, 221 - 244

• Children’s and young people’s response to parental illness: introduction and overview

  Morley DP. and Jenkinson C., (2016), Children and Young People’s Response to Parental Illness: A Handbook of Assessment and Practice, 1 - 4

• Children and Young People’s Response to Parental Illness A Handbook of Assessment and Practice

  Morley DP. et al, (2016)

• Comparing the functioning and well-being of people with motor neurone disease, multiple sclerosis and Parkinson’s disease

  Morley DP. et al, (2016), European Journal of Neurology, 23, 645 - 645

• Development of the Oxford Participation & Activities Questionnaire: Exploring the Views of Relevant Professionals

  Morley D. et al, (2016), Movement Disorders, 29(S1), 179 - 179

• Patient reported outcomes.

  Jenkinson C. and Morley D., (2016), Eur J Cardiovasc Nurs, 15, 112 - 113

• Validation of the Oxford Participation and Activities Questionnaire.

  Morley D. et al, (2016), Patient Relat Outcome Meas, 7, 73 - 80

• The Oxford Participation & Activities Questionnaire (Ox-Paq): Psychometric Analysis.

  Morley D. et al, (2015), Value Health, 18

• Comparing results from long and short form versions of the Parkinson's disease questionnaire in a longitudinal study.

  Jenkinson C. et al, (2015), Parkinsonism Relat Disord, 21, 1312 - 1316

• Comparing results from long and short form versions of the Parkinson's disease questionnaire in a longitudinal study

  Jenkinson C. et al, (2015), Parkinsonism and Related Disorders, 21, 1312 - 1316

• Outcome measurement in neurodegenerative disease: attributes, applications & interpretation.

  Kelly L. et al, (2015), Neurodegener Dis Manag, 5, 305 - 316

• THE PARKINSON'S DISEASE QUESTIONNAIRE (PDQ-39) - EVALUATING THE PSYCHOMETRIC PROPERTIES OF AN ELECTRONIC VERSION

  Morley D. et al, (2015), VALUE IN HEALTH, 18, A286 - A286

• Evaluating the psychometric properties of an e-based version of the 39-item Parkinson's Disease Questionnaire.

  Morley D. et al, (2015), Health Qual Life Outcomes, 13

• The Outcomes and Experiences Questionnaire: development and validation.

  Gibbons E. et al, (2015), Patient Relat Outcome Meas, 6, 179 - 189

• Development of the Oxford Participation and Activities Questionnaire: constructing an item pool.

  Kelly L. et al, (2015), Patient Relat Outcome Meas, 6, 145 - 155

• Evaluating the psychometric properties of an electronic version of the Parkinson’s Disease Questionnaire (PDQ-39)

  Morley D. et al, (2014), Final Program

• An Electronic Version of the Pdq-39: Acceptability To Respondents and Assessment of Alternative Response formats.

  Morley D. et al, (2014), Value Health, 17

• The Outcomes and Experiences Questionnaire (OEQ): Development and Validation

  Gibbons E. et al, (2014), Quality of Life Research, 23(S1)

• Generating items for the Oxford Participation and Activities Questionnaire (Ox-PAQ)

  Kelly L. et al, (2014), Quality of Life Research, 23(S1), 81 - 82

• Transition Questions or Items

  Morley D. et al, (2014), Encyclopedia of Quality of Life and Well-Being Research, 6720 - 6721

• Medical Outcomes Study Short-Form 36-Item Questionnaire.

  Morley D. and Jenkinson, C None., (2014), Encyclopedia of Quality of Life and Well-Being Research, 3972 - 3975

• Acute Myocardial Infarction

  Morley D. and Jenkinson C., (2014), Encyclopedia of Quality of Life and Well-Being Research, 26 - 27

• An electronic version of the PDQ-39: acceptability to respondents and assessment of alternative response formats.

  Morley D. et al, (2014), J Parkinsons Dis, 4, 467 - 472

• Pretesting an electronic version of the PDQ-39.

  Morley D. et al, (2013), Abstracts of the 20th World Congress on Parkinson’s Disease & Related Disorders, 039

• Development of the Oxford Participation & Activities Questionnaire: Semi Structured Interviews with Potential Users

  Morley D. et al, (2013), S1

• Development & Validation of the Oxford Participation & Activities Questionnaire: Exploring the Views of Relevant Stakeholders.

  Kelly L. et al, (2013), Quality of Life Research, 22(S1), 119 - 120

• The PDQ-Carer: development and validation of a summary index score.

  Morley D. et al, (2013), Parkinsonism Relat Disord, 19, 448 - 449

• A structured review of patient reported outcome measures used for cosmetic surgical procedures

  Morley DP. et al, (2013), 1 - 49

• The Oxford Participation and Activities Questionnaire: study protocol.

  Morley D. et al, (2013), Patient Relat Outcome Meas, 5, 1 - 6

• The Manchester-Oxford Foot Questionnaire (MOXFQ): Development and validation of a summary index score.

  Morley D. et al, (2013), Bone Joint Res, 2, 66 - 69

• Furthering our understanding of the needs of adolescent children of parents with Parkinson's disease.

  Morley D. and Jenkinson C., (2013), Adolesc Health Med Ther, 4, 75 - 77

• CARERS OF PEOPLE WITH PARKINSON'S DISEASE: FACTORS RELATED TO QUALITY OF LIFE

  Morley D. et al, (2012), VALUE IN HEALTH, 15, A557 - A557

• A MEASURE OF CARER QUALITY OF LIFE IN PARKINSON'S DISEASE (PDQ-CARER): DEVELOPMENT AND VALIDATION OF A SUMMARY INDEX SCORE

  Jenkinson C. et al, (2012), VALUE IN HEALTH, 15, A556 - A556

• The self-report Barthel Index: preliminary validation in people with Parkinson's disease.

  Morley D. et al, (2012), Eur J Neurol, 19, 927 - 929

• The development and validation of a quality of life measure for the carers of people with Parkinson's disease (the PDQ-Carer)

  Jenkinson C. et al, (2012), Parkinsonism and Related Disorders, 18, 483 - 487

• The development and validation of a quality of life measure for the carers of people with Parkinson's disease (the PDQ-Carer).

  Jenkinson C. et al, (2012), Parkinsonism Relat Disord, 18, 483 - 487

• The Importance of Recognising Depression in Adolescents Affected by Parental Illness

  Morley D. and Jenkinson C., (2012), Psychology, 3, 756 - 757

• Factors related to the Quality of Life of Carers of People with Parkinson’s Disease

  Peters M. et al, (2012), 21, 75 - 76

• Factors influencing quality of life in caregivers of people with Parkinson's disease and implications for clinical guidelines.

  Morley D. et al, (2012), Parkinsons Dis, 2012

• The Psychosocial Impact of Parkinson’s Disease on the Wider Family Unit: A Focus on the Offspring of Affected Individuals

  Morley D., (2011), Symptoms of Parkinson's Disease

• Predictors of quality of life in Polish immigrants living in London

  Suszynska W. and Morley D., (2011)

• Adolescent and Adult Children of Parents with Parkinson's Disease: Incorporating Their Needs in Clinical Guidelines

  Morley D. et al, (2011), Parkinson's Disease, 2011

• Refinement and validation of the Parental Illness Impact Scale.

  Morley D. et al, (2010), Parkinsonism Relat Disord, 16, 181 - 185

• Sibling Support & Adjustment to Parental Neurological Illness. International Society for Quality of Life Research ~ 2010 Conference Abstracts

  Morley D. and Selai C., (2010), 19, 1 - 144

• Health Related Quality of Life in Gilles de la Tourette Syndrome: Development and Validation of the GTS-QOL.

  Cavanna AE. et al, (2009), 80, 815 - 828

• The Gilles de la Tourette Syndrome–Quality of Life Scale (GTS-QOL): Development and validation

  Cavanna AE. et al, (2008), Neurology, 71, 1410 - 1416

• Preliminary validation of the self-report Barthel Index in people with Parkinson’s disease

  Morley D. et al, (2008), 15, 32 - 220

• Understanding the role of non-residential stepmothers in developing successful stepfamilies (R) 406-39

  Doodson L. and Morley D., (2007)

• Quality of life and psychosocial well-being in people with multiple sclerosis and Parkinson’s disease

  Morley D. et al, (2007)

• Health-related quality of life in Gilles de la Tourette syndrome

  Cavanna A. et al, (2007), 78, 780 - 786

• When children grow up with a chronically ill parent

  Morley D., (2006), 21, S1 - S51

• Understanding the Roles of Non-Residential Stepmothers

  Doodson L. and Morley D., (2006), Journal of Divorce & Remarriage, 45, 109 - 130

• Further development and validation of the Parental Illness Impact Scale

  Morley D. et al, (2006), 21

• Comparing caregiver anxiety across chronic and acute neurological conditions

  Morley D. et al, (2006), 189 - 195

• Caregiver-burden in parkinson's disease is closely associated with psychiatric symptoms, falls, and disability

  Schrag A. et al, (2006), Parkinsonism & related disorders, 12, 35 - 41

• Assessing the Impact of Parental Illness on Adolescent and Adult Children

  Morley D. et al, (2005), 14

• Impact of Parkinson’s disease on patients’ adolescent and adult children

  Schrag A. et al, (2004), 19

• Impact of Parkinson's disease on patients' adolescent and adult children

  Schrag A. et al, (2004), Parkinsonism & Related Disorders, 10, 391 - 397

• Factors contributing to caregiver burden and carer quality of life

  Schrag A. et al, (2004), Movement Disorders, 19

• Development of a measure of the impact of chronic parental illness on adolescent and adult children. The Parental Illness Impact Scale (Parkinson's disease)

  Schrag A. et al, (2004), Parkinsonism & Related Disorders, 10, 399 - 405

• Young- versus older-onset Parkinson's disease: Impact of disease and psychosocial consequences

  Schrag A. et al, (2003), Movement Disorders, 18, 1250 - 1256

• Poster session 3: Parkinson's Disease

  (2002), Movement Disorders, 17, S115 - S165

• Impact of parental illness on adolescent and adult children of patients with Parkinson’s disease

  Jahanshahi M. et al, (2002), Movement Disorders, 17, S115 - S165

• Results from Pretesting an Electronic Version of the PDQ-39

  Morley D. et al, Movement Disorders, 29(S1)

Recent Publications

• Pretesting an e-based version of the Oxford Participation and Activities Questionnaire (Ox-PAQ)

  Kelly L. et al, (2016), Value in Health, 19, A485 - A485

• Use of the Routine Activities Domain of the Oxford Participation & Activities Questionnaire (Ox-PAQ)

  Kelly L. et al, (2016), Quality of Life Research, 25, 106 - 106

• Underinvestigated parental conditions: an overview

  Kelly L. and Morley DP., (2016), Children’s and young people’s response to parental illness, 153 - 170

• Parental Parkinson’s disease

  Morley DP. and Book E., (2016), Children’s and young people’s response to parental illness, 23 - 36

• Measuring the impact of parental illness

  Kelly L. et al, (2016), Children’s and young people’s response to parental illness, 221 - 244