916 results on '"Jenkinson, Crispin"'
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102. Should Breast Reduction Surgery Be Rationed? A Comparison Of The Health Status Of Patients Before And After Treatment: Postal Questionnaire Survey
103. Evidence for the Sensitivity of the SF-36 Health Status Measure to Inequalities in Health: Results from the Oxford Healthy Lifestyles Survey
104. Evaluation of the Dutch version of the Parkinson's Disease Questionnaire 39
105. The current practice of handling and reporting missing outcome data in eight widely-used PROMS in RCT publications: are we doing well?
106. Development of an Exercise‐Specific Parkinson's Disease Questionnaire: The PDQ‐Exercise
107. Carers using assistive technology in dementia care: an explanatory sequential mixed methods study
108. Development of a core outcome set for lower limb orthopaedic surgical interventions in ambulant children and young people with cerebral palsy: A study protocol
109. Young People’s Response to Parental Neurological Disorder: A Structured Review
110. Patient reported outcomes
111. Cross-cultural evaluation of the short form 8-item Parkinson's Disease Questionnaire (PDQ-8): Results from America, Canada, Japan, Italy and Spain
112. The Parkinson's Disease Questionnaire (PDQ-39): evidence for a method of imputing missing data
113. Using rapid cycle tests of change to develop the Carers Assistive Technology Experience Questionnaire: a cognitive interview study in the UK
114. Health-Related Quality of Life in Amyotrophic Lateral Sclerosis: Determining a Meaningful Deterioration
115. Evaluating the responsiveness of the endometriosis health profile questionnaire: The EHP-30
116. Development of the Short Form Endometriosis Health Profile Questionnaire: The EHP-5
117. The Stroke Impact Scale: Validation in a UK Setting and Development of a SIS Short Form and SIS Index
118. Use of the short form health survey (SF-36) in patients with amyotrophic lateral sclerosis: tests of data quality, score reliability, response rate and scaling assumptions
119. Aspects of methodology relevant to patient-reported outcome measures (PROMs)
120. The development and validation of the Parkinson's Disease Questionnaire and related measures
121. Health selection in the Whitehall II study, UK
122. Comparing health inequalities among men aged 18-65 years in Australia and England using the SF-36
123. Fabry International Prognostic Index: a predictive severity score for Anderson-Fabry disease
124. Development and validation of a short measure of health status for individuals with amyotrophic lateral sclerosis/ motor neurone disease: the ALSAQ-40
125. Health-Related Quality-of-Life Measurement in Patients with Parkinson’s Disease
126. Carers’ Experiences of Assistive Technology Use in Dementia Care: A Cross Sectional Survey
127. Development of a core outcome set for lower limb orthopaedic surgical interventions in ambulant children and young people with cerebral palsy: a study protocol
128. Carers’ experience of using assistive technology for dementia care at home: a qualitative study
129. Web-Based and mHealth Technologies to Support Self-Management in People Living With Type 2 Diabetes: Validation of the Diabetes Self-Management and Technology Questionnaire (DSMT-Q) (Preprint)
130. The routine use of patient reported outcome measures in healthcare settings
131. Social and psychological factors affecting the impact of painful chronic illness upon mental health
132. Comparison of therapeutic and subtherapeutic nasal continuous positive airway pressure for obstructive sleep apnoea: a randomised prospective parallel trial
133. Measuring patientsʼ experiences and outcomes
134. Outcome measures used in forensic mental health research: a structured review
135. Multi-center studies of the global impact of endometriosis and the predictive value of associated symptoms
136. Additional file 2: of Informal carersâ experience and outcomes of assistive technology use in dementia care in the community: a systematic review protocol
137. Additional file 2: of Informal carersâ experience of assistive technology use in dementia care at home: a systematic review
138. Additional file 4: of Informal carersâ experience and outcomes of assistive technology use in dementia care in the community: a systematic review protocol
139. Additional file 1: of Informal carersâ experience of assistive technology use in dementia care at home: a systematic review
140. Additional file 3: of Informal carersâ experience of assistive technology use in dementia care at home: a systematic review
141. Additional file 1: of Informal carersâ experience and outcomes of assistive technology use in dementia care in the community: a systematic review protocol
142. Additional file 3: of Informal carersâ experience and outcomes of assistive technology use in dementia care in the community: a systematic review protocol
143. Additional file 4: of Informal carersâ experience of assistive technology use in dementia care at home: a systematic review
144. Social survey research
145. THE SCIENTIFIC ASSESSMENT OF SUBJECTIVE OUTCOME AFTER LAPAROSCOPIC UROLOGICAL PROCEDURES
146. Comparison of medical and nursing attitudes to resuscitation and patient autonomy between a British and an American teaching hospital
147. Measuring quality of life in women with endometriosis: tests of data quality, score reliability, response rate and scaling assumptions of the Endometriosis Health Profile Questionnaire
148. The Parkinson's Disease Questionnaire (PDQ-39): development and validation of a Parkinson's disease summary index score
149. Evaluation of treatment for congestive heart failure in patients aged 60 years and older using generic measures of health status (SF-36 and COOP charts)
150. Patient attitudes to clinical trials: development of a questionnaire and results from asthma and cancer patients
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