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Patient issues in health research and quality of care: an inventory and data synthesis.

Patient issues in health research and quality of care: an inventory and data synthesis.

http://www.wikidata.org/entity/Q33965420

about

Data monitoring committees for pragmatic clinical trials.There are some big changes at Health Expectations.Developing a patient and family research advisory panel to include people with significant disease, multimorbidity and advanced age.Giving voice to older adults living with frailty and their family caregivers: engagement of older adults living with frailty in research, health care decision making, and in health policy.Collaborative Patient-Centered Quality Improvement: A Cross-Sectional Survey Comparing the Types and Numbers of Quality Initiatives Selected by Patients and Health Professionals.Inspectors' responses to adolescents' assessment of quality of care: a case study on involving adolescents in inspections.Engaging older adults in healthcare research and planning: a realist synthesis.

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Patient issues in health research and quality of care: an inventory and data synthesis.

http://www.wikidata.org/entity/Q33965420

description

2011 nî lūn-bûn

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2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2011 թվականի հուլիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Patient issues in health research and quality of care: an inventory and data synthesis.

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Patient issues in health research and quality of care: an inventory and data synthesis.

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Patient issues in health research and quality of care: an inventory and data synthesis.

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J.1369-7625.2011.00718.X

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Health Expectations

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Patient issues in health research and quality of care: an inventory and data synthesis.

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Merel Visse

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Pim de Boer

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Tineke A Abma

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Truus Teunissen

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P2860

Methods of consumer involvement in developing healthcare policy and research, clinical practice guidelines and patient information material

Ethnic minorities and prescription medication; concordance between self-reports and medical records.

Lifeworld-led healthcare is more than patient-led care: an existential view of well-being.

Patients as partners in responsive research: methodological notions for collaborations in mixed research teams.

Patient participation as dialogue: setting research agendas.

Involving consumers in research and development agenda setting for the NHS: developing an evidence-based approach.

Patient participation in collective healthcare decision making: the Dutch model.

Patient-expert partnerships in research: how to stimulate inclusion of patient perspectives.

Dialogue for air, air for dialogue: towards shared responsibilities in COPD practice.

The rights of the patient in clinical research.

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quality of care

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