| P50 | author | Line Bjørnskov Pedersen | Q57895222 |
| | G. Ardine de Wit | Q60669638 |
| | Marcel Heldoorn | Q77542611 |
| | Esther W de Bekker-Grob | Q91539297 |
| | Mattijs S Lambooij | Q93150450 |
| P2093 | author name string | Ewout W Steyerberg | |
| | Dorte Gyrd-Hansen | |
| | Domino Determann | |
| P2860 | cites work | Personal health records: definitions, benefits, and strategies for overcoming barriers to adoption. | Q24544267 |
| | The value of personal health record (PHR) systems | Q24657644 |
| | Potential of electronic personal health records | Q24679376 |
| | The impact of electronic patient portals on patient care: a systematic review of controlled trials | Q26866084 |
| | Patient Portals and Patient Engagement: A State of the Science Review | Q28081888 |
| | Exploring challenges and potentials of personal health records in diabetes self-management: implementation and initial assessment | Q28257156 |
| | Perceptions of chronically ill and healthy consumers about electronic personal health records: a comparative empirical investigation | Q30391104 |
| | It Ain't Necessarily So: The Electronic Health Record And The Unlikely Prospect Of Reducing Health Care Costs | Q30483159 |
| | Using conjoint analysis to elicit preferences for health care | Q33801139 |
| | A personally controlled electronic health record for Australia | Q33832826 |
| | Designing patient-centered personal health records (PHRs): health care professionals' perspective on patient-generated data | Q34285539 |
| | Improving personal health records for patient-centered care | Q34399904 |
| | Systematic review: impact of health information technology on quality, efficiency, and costs of medical care | Q34526595 |
| | Free Web-based personal health records: an analysis of functionality. | Q35039818 |
| | Personal health records: a scoping review | Q35082969 |
| | Patient and provider attitudes toward the use of patient portals for the management of chronic disease: a systematic review | Q35223214 |
| | Organizational strategies for promoting patient and provider uptake of personal health records | Q35611246 |
| | "Nothing About Me Without Me": An Interpretative Review of Patient Accessible Electronic Health Records | Q35922465 |
| | Barriers and Facilitators to Online Portal Use Among Patients and Caregivers in a Safety Net Health Care System: A Qualitative Study | Q36440785 |
| | Use of the internet and an online personal health record system by US veterans: comparison of Veterans Affairs mental health service users and other veterans nationally | Q36500494 |
| | Nominal group technique to select attributes for discrete choice experiments: an example for drug treatment choice in osteoporosis | Q36610799 |
| | Barriers and Facilitators of Online Patient Portals to Personal Health Records Among Persons Living With HIV: Formative Research | Q36771520 |
| | Costs and benefits of health information technology | Q36879089 |
| | Which Users Should Be the Focus of Mobile Personal Health Records? Analysis of User Characteristics Influencing Usage of a Tethered Mobile Personal Health Record | Q36882088 |
| | Exploring technology impacts of Healthcare 2.0 initiatives | Q37453457 |
| | The value of personal health records for chronic disease management: what do we know? | Q37873865 |
| | Constructing experimental designs for discrete-choice experiments: report of the ISPOR Conjoint Analysis Experimental Design Good Research Practices Task Force | Q38075667 |
| | A review of the empirical evidence of the healthcare benefits of personal health records | Q38131305 |
| | Electronic patient portals: evidence on health outcomes, satisfaction, efficiency, and attitudes: a systematic review | Q38163852 |
| | Discrete choice experiments in health economics: a review of the literature | Q38227517 |
| | The evolution of personal health records and their role for self-management: a literature review | Q38243650 |
| | Conjoint analysis applications in health--a checklist: a report of the ISPOR Good Research Practices for Conjoint Analysis Task Force | Q39739727 |
| | Consumer attitudes toward personal health records in a beacon community. | Q39991645 |
| | What it takes: characteristics of the ideal personal health record | Q39996147 |
| | Patient Access to Personal Health Information: Regulation vs. Reality | Q40065907 |
| | Conducting discrete choice experiments to inform healthcare decision making: a user's guide. | Q40071854 |
| | Discrete choice experiments in health care | Q43159218 |
| | A New Approach to Consumer Theory | Q55953685 |
| | Simultaneous conjoint measurement: A new type of fundamental measurement | Q55954423 |
| | A comparison of approaches to estimating confidence intervals for willingness to pay measures | Q79611544 |
| | Determinants of personal health record use: a large population study at Cleveland Clinic | Q83300242 |
| | Applicability of internationally available health literacy measures in the Netherlands | Q84996795 |
| | Personal health records: Consumer attitudes toward privacy and security of their personal health information | Q87607855 |
| P433 | issue | 3 | |
| P921 | main subject | Netherlands | Q55 |
| P304 | page(s) | 529-536 | |
| P577 | publication date | 2017-05-01 | |
| P1433 | published in | Journal of the American Medical Informatics Association | Q152037 |
| P1476 | title | Personal health records in the Netherlands: potential user preferences quantified by a discrete choice experiment | |
| P478 | volume | 24 | |