Sharing medical data for health research: the early personal health record experience. - Wikidata - awgldk - TriplyDB

Sharing medical data for health research: the early personal health record experience.

Sharing medical data for health research: the early personal health record experience.

http://www.wikidata.org/entity/Q33587069

about

Big Data and Comparative Effectiveness Research in Radiation Oncology: Synergy and Accelerated Discovery.Comparison of consumers' views on electronic data sharing for healthcare and research What Online User Innovation Communities Can Teach Us about Capturing the Experiences of Patients Living with Chronic Health Conditions. A Scoping Review Sharing my health data: a survey of data sharing preferences of healthy individuals The use of electronic patient records for medical research: conflicts and contradictions Participatory surveillance of diabetes device safety: a social media-based complement to traditional FDA reporting Are personal health records safe? A review of free web-accessible personal health record privacy policies Willingness to share personal health record data for care improvement and public health: a survey of experienced personal health record users Sharing data for public health research by members of an international online diabetes social network Big data, advanced analytics and the future of comparative effectiveness research.The Future of Patient Engagement in the Governance of Shared Data.Protocol for a randomised controlled trial examining the impact of a web-based personally controlled health management system on the uptake of influenza vaccination rates.Helping high-risk youth move through high-risk periods: personally controlled health records for improving social and health care transitions.Learning relational policies from electronic health record access logs.The future of medical diagnostics: large digitized databases.Factors affecting willingness to share electronic health data among California consumers.Use of Patient Portals for Personal Health Information Management: The Older Adult Perspective.Patient informed governance of distributed research networks: results and discussion from six patient focus groups Innovative uses of electronic health records and social media for public health surveillance.Use of electronic patient records for research: views of patients and staff in general practice.Stakeholders' views on data sharing in multicenter studies.Protected health information on social networking sites: ethical and legal considerations.Personalized Consent Flow in Contemporary Data Sharing for Medical Research: A Viewpoint.Patient preferences toward an interactive e-consent application for research using electronic health records.Perceptions of the uses of routine general practice data beyond individual care in England: a qualitative study.Availability and quality of mobile health app privacy policies.Society and personal genome data.

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P2860

Sharing medical data for health research: the early personal health record experience.

http://www.wikidata.org/entity/Q33587069

description

2010 nî lūn-bûn

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2010 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2010 թվականի մայիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Sharing medical data for health research: the early personal health record experience.

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Sharing medical data for health research: the early personal health record experience.

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Journal of Medical Internet Research

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Sharing medical data for health research: the early personal health record experience.

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Elissa R Weitzman

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Kenneth D Mandl

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Liljana Kaci

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P2860

Social uses of personal health information within PatientsLikeMe, an online patient community: what can happen when patients have access to one another's data

Indivo: a personally controlled health record for health information exchange and communication

Acceptability of a personally controlled health record in a community-based setting: implications for policy and design

Alternatives to project-specific consent for access to personal information for health research: insights from a public dialogue

Clinical governance and research ethics as barriers to UK low-risk population-based health research?

Consent for use of personal information for health research: do people with potentially stigmatizing health conditions and the general public differ in their opinions?

Integrated personal health records: transformative tools for consumer-centric care.

National survey of British public's views on use of identifiable medical data by the National Cancer Registry.

Integration of the personally controlled electronic medical record into regional inter-regional data exchanges: a national demonstration.

The genetic liability to disability retirement: a 30-year follow-up study of 24,000 Finnish twins.

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10.2196/JMIR.1356

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2

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12

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2010-05-25T00:00:00Z

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