Sara Riggare

发表

Participatory design in Parkinson's research with focus on the symptomatic domains to be measured.

Walter Maetzler, Frank Larsen, Holm Graessner, 2015, Journal of Parkinson's disease.

Precision Medicine in Parkinson’s Disease – Exploring Patient-Initiated Self-Tracking

Sara Riggare, M. Hägglund, 2018, Journal of Parkinson's disease.

Deep Phenotyping of Parkinson’s Disease

Max A. Little, Mohammad Rafayet Ali, Alistair M. Glidden, 2020, Journal of Parkinson's disease.

Patient-driven N-of-1 in Parkinson’s Disease

Kenton T. Unruh, P. Svenningsson, J. Stamford, 2017, Methods of Information in Medicine.

E-patients hold key to the future of healthcare

Sara Riggare, 2018, British Medical Journal.

Dyskinesia Matters

R. Pahwa, D. Eidelberg, R. Hauser, 2019, Movement disorders : official journal of the Movement Disorder Society.

Sham neurosurgical procedures: the patients' perspective

Sara Riggare, P. Cohen, T. Isaacs, 2012, The Lancet Neurology.

Patient-Centric Strategies in Digital Health

Sara Riggare, L. Chu, Jamison G Gamble, 2018 .

From Information Seekers to Innovators: Qualitative Analysis Describing Experiences of the Second Generation of E-Patients

S. Koch, L. Sharp, Sara Riggare, 2019, Journal of medical Internet research.

Meeting the Burden of Self-management: Qualitative Study Investigating the Empowering Behaviors of Patients and Informal Caregivers

S. Koch, Sara Riggare, M. Hägglund, 2022, Journal of participatory medicine.

From Information Seekers to Innovators: Qualitative Analysis Describing Experiences of the Second Generation of E-Patients (Preprint)

S. Koch, L. Sharp, Sara Riggare, 2019 .

National randomized controlled trial of virtual house calls for Parkinson disease

Z. Mari, C. Tanner, N. Galifianakis, 2017, Neurology.

Erratum To: Virtual house calls for Parkinson disease (Connect.Parkinson): study protocol for a randomized, controlled trial

E. Dorsey, C. Boyd, K. Biglan, 2016, Trials.

Individually Tailored Internet-Based Cognitive-Behavioral Therapy for Daily Functioning in Patients with Parkinson’s Disease: A Randomized Controlled Trial

G. Andersson, P. Svenningsson, N. Lindefors, 2020, Journal of Parkinson's disease.

Patient-driven innovations reported in peer-reviewed journals: a scoping review

J. Øvretveit, Pamela Mazzocato, H. Hasson, 2022, BMJ Open.

Patients are doing it for themselves: A survey on disease-specific knowledge acquisition among people with Parkinson’s disease in Sweden

Maria Hägglund, Per Svenningsson, Sara Riggare, 2017, Health Informatics J..

National Randomized Controlled Trial of Virtual House Calls for People with Parkinson's Disease: Interest and Barriers.

Michael T. Bull, Z. Mari, C. Tanner, 2016, Telemedicine journal and e-health : the official journal of the American Telemedicine Association.

Patient lead users experience of the COVID-19 pandemic: a qualitative interview study

H. Hasson, Sara Riggare, T. Stenfors, 2022, BMJ Open.

“You have to know why you're doing this”: a mixed methods study of the benefits and burdens of self-tracking in Parkinson's disease

Maria Hägglund, Sara Riggare, Therese Scott Duncan, 2019, BMC Medical Informatics and Decision Making.

Six countries, six individuals: resourceful patients navigating medical records in Australia, Canada, Chile, Japan, Sweden and the USA

T. Delbanco, Janice Walker, Sara Riggare, 2020, BMJ Open.

Self referral to physiotherapy and other services would empower patients and doctors

Sara Riggare, 2016, British medical journal.

Virtual house calls for Parkinson disease (Connect.Parkinson): study protocol for a randomized, controlled trial

E Ray Dorsey, Cynthia M Boyd, E. Dorsey, 2014, Trials.

A Long Way to Go: Patient Perspectives on Digital Health for Parkinson’s Disease

J. Stamford, Sara Riggare, M. Hägglund, 2021, Journal of Parkinson's disease.

Implementation of a Community-Based Exercise Program for Parkinson Patients: Using Boxing as an Example

B. Bloem, J. Ferreira, M. Graziano, 2019, Journal of Parkinson's disease.

Empowered patients and informal care-givers as partners?—a survey study of healthcare professionals’ perceptions

S. Koch, L. Sharp, Sara Riggare, 2023, BMC Health Services Research.

Patients organise and train doctors to provide better care

Kenton T. Unruh, Sara Riggare, Sara Riggare, 2015, BMJ : British Medical Journal.

Objectives and outcomes of patient-driven innovations published in peer-reviewed journals: a qualitative analysis of publications included in a scoping review

H. Hasson, M. Dahlberg, C. Wannheden, 2023, BMJ Open.

Patient-driven N-of-1 in Parkinson’s Disease Lessons Learned from a Placebo-controlled Study of the Effect of Nicotine on Dyskinesia

Kenton T. Unruh, P. Svenningsson, Josefa Domingos, 2017 .

Ethical Aspects of Personal Science for Persons with Parkinson’s Disease: What Happens When Self-Tracking Goes from Selfcare to Publication?

B. Bloem, M. de Groot, A. Bredenoord, 2021, Journal of Parkinson's disease.

A rocky road but worth the drive: A longitudinal qualitative study of patient innovators and researchers cocreating research

H. Hasson, C. Wannheden, Sara Riggare, 2023, Health expectations : an international journal of public participation in health care and health policy.

MIT Open Access Articles Deep Phenotyping of Parkinson’s Disease

S. Saria, L. Omberg, Zachary Kabelac, 2022 .