Sharing health data for better outcomes on PatientsLikeMe - Wikidata - wikimedia - TriplyDB

Sharing health data for better outcomes on PatientsLikeMe

Sharing health data for better outcomes on PatientsLikeMe

http://www.wikidata.org/entity/Q28748833

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The Role of Social Network Technologies in Online Health Promotion: A Narrative Review of Theoretical and Empirical Factors Influencing Intervention Effectiveness Patient-reported outcomes as a source of evidence in off-label prescribing: analysis of data from PatientsLikeMe A new dimension of health care: systematic review of the uses, benefits, and limitations of social media for health communication Social Media and HIV: A Systematic Review of Uses of Social Media in HIV Communication Health and illness in a connected world: how might sharing experiences on the internet affect people's health?Research Conducted Using Data Obtained through Online Communities: Ethical Implications of Methodological Limitations The Potential of Social Media and Internet-Based Data in Preventing and Fighting Infectious Diseases: From Internet to Twitter Patients optimizing epilepsy management via an online community: the POEM Study Crowdsourced health research studies: an important emerging complement to clinical trials in the public health research ecosystem Social media use in healthcare: A systematic review of effects on patients and on their relationship with healthcare professionals What Online User Innovation Communities Can Teach Us about Capturing the Experiences of Patients Living with Chronic Health Conditions. A Scoping Review Using Social Media for Actionable Disease Surveillance and Outbreak Management: A Systematic Literature Review More Than Telemonitoring: Health Provider Use and Nonuse of Life-Log Data in Irritable Bowel Syndrome and Weight Management Using social media to engage adolescents and young adults with their health Size matters: how population size influences genotype-phenotype association studies in anonymized data Systems Medicine 2.0: potential benefits of combining electronic health care records with systems science models openSNP--a crowdsourced web resource for personal genomics Participant-Centric Initiatives: Tools to Facilitate Engagement In Research Investigating the congruence of crowdsourced information with official government data: the case of pediatric clinics Quality of life in organ transplant recipients participating in an online transplant community Using online health communities to deliver patient-centered care to people with chronic conditions Portal for Families Overcoming Neurodevelopmental Disorders (PFOND): Implementation of a Software Framework for Facilitated Community Website Creation by Nontechnical Volunteers Web 2.0 for health promotion: reviewing the current evidence Implications of Internet availability of genomic information for public health practice Sharing data for public health research by members of an international online diabetes social network Hospital-based nurses' perceptions of the adoption of Web 2.0 tools for knowledge sharing, learning, social interaction and the production of collective intelligence Features of mobile diabetes applications: review of the literature and analysis of current applications compared against evidence-based guidelines Computer-assisted update of a consumer health vocabulary through mining of social network data Big Data in Science and Healthcare: A Review of Recent Literature and Perspectives. Contribution of the IMIA Social Media Working Group.Making sense of the shadows: priorities for creating a learning healthcare system based on routinely collected data Can data repositories help find effective treatments for complex diseases?The Role of Big Data in the Management of Sleep-Disordered Breathing.Development of a Smartphone App for a Genetics Website: The Amyotrophic Lateral Sclerosis Online Genetics Database (ALSoD).A European network of email and telephone help lines providing information and support on rare diseases: results from a 1-month activity survey Uncovering patterns of technology use in consumer health informatics.Effects of eHealth Literacy on General Practitioner Consultations: A Mediation Analysis.What explains usage of mobile physician-rating apps? Results from a web-based questionnaire Power to the people: participant ownership of clinical trial data.ePatients on YouTube: analysis of four experiences from the patients' perspective.Accelerated clinical discovery using self-reported patient data collected online and a patient-matching algorithm.

P2860

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P2860

Sharing health data for better outcomes on PatientsLikeMe

http://www.wikidata.org/entity/Q28748833

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2010 nî lūn-bûn

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2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2010 թվականի հունիսին 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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Sharing health data for better outcomes on PatientsLikeMe

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Sharing health data for better outcomes on PatientsLikeMe

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Sharing health data for better outcomes on PatientsLikeMe

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Sharing health data for better outcomes on PatientsLikeMe

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Journal of Medical Internet Research

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Sharing health data for better outcomes on PatientsLikeMe

@en

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James Heywood

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Jeana Frost

http://www.w3.org/2001/XMLSchema#string

Michael Massagli

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Richard Bradley

http://www.w3.org/2001/XMLSchema#string

Sally Okun

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Timothy Vaughan

http://www.w3.org/2001/XMLSchema#string

P2860

Information from the Internet and the doctor-patient relationship: the patient perspective--a qualitative study

Are physicians ready for patients with Internet-based health information?

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

Analysis of cases of harm associated with use of health information on the internet

ALS patients request more information about cognitive symptoms

Assessing the privacy risks of data sharing in genomics

Emerging patient-driven health care models: an examination of health social networks, consumer personalized medicine and quantified self-tracking

PatientsLikeMe: Consumer health vocabulary as a folksonomy

Are patients' office visits with physicians getting shorter?

E-mail in patient-provider communication: a systematic review.

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scholarly article

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987162

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10.2196/JMIR.1549

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2

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12

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Catherine A. Brownstein

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2010-06-14T00:00:00Z

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44668228

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20542858

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2956230

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