(Q34078657)

30 July 2017

title

Perceived benefits of sharing health data between people with epilepsy on an online platform (English)

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30 July 2017

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Catherine A. Brownstein

object named as

Catherine Brownstein

5

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Paul Wicks

object named as

Paul Wicks

1

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author name string

Dorothy L Keininger

2

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30 July 2017

Michael P Massagli

3

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30 July 2017

Christine de la Loge

4

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30 July 2017

Jouko Isojärvi

6

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30 July 2017

James Heywood

7

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30 July 2017

publication date

17 November 2011

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30 July 2017

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30 July 2017

volume

23

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30 July 2017

issue

1

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30 July 2017

page(s)

16-23

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What do people with epilepsy know about their condition? Evaluation of a subspecialty clinic population

30 July 2017

cites work

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.09.026

The global burden and stigma of epilepsy

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Epilepsy stigma: what do we know and where next?

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Receiving social support online: implications for health education

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Information exchange in an epilepsy forum on the World Wide Web

7 January 2021

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The first generation of e-patients

7 January 2021

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Use of computers and the Internet for health information by patients with epilepsy

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.09.026

The Influence of Social Support on Chronic Illness Self-Management: A Review and Directions for Research

7 January 2021

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Patient compliance with paper and electronic diaries

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.09.026

Evaluation of WebEase: an epilepsy self-management Web site

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.09.026

The prevention research centers' managing epilepsy well network

7 January 2021

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How to get the answer to nearly everything: using the internet for epilepsy research.

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Using the Internet to recruit patients for epilepsy trials: results of a New Zealand pilot study

7 January 2021

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7 January 2021

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Fostering empowerment in online support groups

7 January 2021

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Living with HIV/AIDS and use of online support groups.

7 January 2021

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Internet use and stigmatized illness.

7 January 2021

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The role of online support communities: benefits of expanded social networks to patients with psoriasis.

7 January 2021

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Social networks and collateral health effects

7 January 2021

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Sharing health data for better outcomes on PatientsLikeMe

7 January 2021

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Patient-reported outcomes as a source of evidence in off-label prescribing: analysis of data from PatientsLikeMe

7 January 2021

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Accelerated clinical discovery using self-reported patient data collected online and a patient-matching algorithm

7 January 2021

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Development and cross-cultural translations of a 31-item quality of life in epilepsy inventory

7 January 2021

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The hospital anxiety and depression scale

7 January 2021

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EQ-5D: a measure of health status from the EuroQol Group

7 January 2021

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Examining the relationships of depressive symptoms, stigma, social support and regimen-specific support on quality of life in adult patients with epilepsy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.09.026

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.09.026

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

7 January 2021

1 reference

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

7 January 2021

1 reference

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The physician-patient relationship and a National Health Information network

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2011.09.026

Survey results of Internet and computer usage in veterans with epilepsy

7 January 2021

1 reference

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10.1016/J.YEBEH.2011.09.026

7 January 2021

Identifiers

DOI

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30 July 2017

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