| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acknowledgement to Referees
|
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|
1 |
p. 1-2
|
artikel
|
| 2 |
Acknowledgement to Referees
|
|
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|
1 |
p. 1-2
|
artikel
|
| 3 |
Acknowledgement to Referees
|
|
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|
1 |
p. 1-3
|
artikel
|
| 4 |
Acknowledgement to Referees
|
|
|
|
|
1 |
p. 1-2
|
artikel
|
| 5 |
A Comparison of Analytic Hierarchy Process and Conjoint Analysis Methods in Assessing Treatment Alternatives for Stroke Rehabilitation
|
Ijzerman, Maarten J.
|
|
2012
|
|
1 |
p. 45-56
|
artikel
|
| 6 |
A Conceptual Model of Angelman Syndrome and Review of Relevant Clinical Outcomes Assessments (COAs)
|
Grieco, Joseph C.
|
|
2018
|
|
1 |
p. 97-112
|
artikel
|
| 7 |
Adopting a Sustainable Community of Practice Model when Developing a Service to Support Patients with Epidermolysis Bullosa (EB): A Stakeholder-Centered Approach
|
Gowran, Rosemary Joan
|
|
2014
|
|
1 |
p. 51-63
|
artikel
|
| 8 |
Age and Choice in Health Insurance
|
Becker, Karolin
|
|
2008
|
|
1 |
p. 27-40
|
artikel
|
| 9 |
Aligning Research and Practice: Implications of Patient-Centered Care for Placebo Effects
|
Geers, Andrew L.
|
|
2013
|
|
1 |
p. 1-3
|
artikel
|
| 10 |
An Asia Pacific Alliance for Rare Diseases
|
Wong-Rieger, Durhane
|
|
2014
|
|
1 |
p. 11-17
|
artikel
|
| 11 |
An Evidence-Based Theory About PRO Use in Kidney Care: A Realist Synthesis
|
Schick-Makaroff, Kara
|
|
|
|
1 |
p. 21-38
|
artikel
|
| 12 |
An Introduction to Item Response Theory for Patient-Reported Outcome Measurement
|
Nguyen, Tam H.
|
|
2014
|
|
1 |
p. 23-35
|
artikel
|
| 13 |
A Qualitative Study on Feasibility of a Web-Based Women’s Health Portal and Information System
|
Yang, Min
|
|
2011
|
|
1 |
p. 67-68
|
artikel
|
| 14 |
Assessing Preferences Regarding Healthcare Interventions that Involve Non-Health Outcomes
|
Opmeer, Brent C.
|
|
2010
|
|
1 |
p. 1-10
|
artikel
|
| 15 |
Assessment of Transdermal Buprenorphine Patches for the Treatment of Chronic Pain in a UK Observational Study
|
Serpell, Mick
|
|
2015
|
|
1 |
p. 35-46
|
artikel
|
| 16 |
A Systematic and Critical Review of Discrete Choice Experiments in Asthma and Chronic Obstructive Pulmonary Disease
|
Collacott, Hannah
|
|
|
|
1 |
p. 55-68
|
artikel
|
| 17 |
A Systematic Review and Meta-Synthesis of Patients’ Experiences and Perceptions of Seeking and Using Benzodiazepines and Z-Drugs: Towards Safer Prescribing
|
Sirdifield, Coral
|
|
2016
|
|
1 |
p. 1-15
|
artikel
|
| 18 |
A Systematic Review of Discrete Choice Experiments and Conjoint Analysis on Genetic Testing
|
Ozdemir, Semra
|
|
|
|
1 |
p. 39-54
|
artikel
|
| 19 |
Authors’ Reply to Montoya et al. Comment On: “Tools Measuring Quality of Death, Dying, and Care, Completed After Death: Systematic Review of Psychometric Properties”
|
Kupeli, Nuriye
|
|
2018
|
|
1 |
p. 169
|
artikel
|
| 20 |
Benefit–Risk or Risk–Benefit Trade-Offs? Another Look at Attribute Ordering Effects in a Pilot Choice Experiment
|
Heidenreich, Sebastian
|
|
|
|
1 |
p. 65-74
|
artikel
|
| 21 |
Burden of a Multiple Sclerosis Relapse
|
Oleen-Burkey, MerriKay
|
|
2012
|
|
1 |
p. 57-69
|
artikel
|
| 22 |
Caregiver Preferences for Emerging Duchenne Muscular Dystrophy Treatments: A Comparison of Best-Worst Scaling and Conjoint Analysis
|
Hollin, Ilene L.
|
|
2014
|
|
1 |
p. 19-27
|
artikel
|
| 23 |
Challenges in Measuring the Societal Value of Orphan Drugs: Insights from a Canadian Stated Preference Survey
|
Dragojlovic, Nick
|
|
2015
|
|
1 |
p. 93-101
|
artikel
|
| 24 |
Challenges of Realising Patient-Centred Outcomes for Deaf Patients
|
Rogers, Katherine D.
|
|
2017
|
|
1 |
p. 9-16
|
artikel
|
| 25 |
Comment on “Feasibility of Measuring Preferences for Chemotherapy Among Early-Stage Breast Cancer Survivors Using a Direct Rank Ordering Multicriteria Decision Analysis Versus a Time Trade-Off”
|
Kujawski, Edouard
|
|
|
|
1 |
p. 145-146
|
artikel
|
| 26 |
Comment on: Tools Measuring Quality of Death, Dying, and Care, Completed After Death: Systematic Review of Psychometric Properties
|
Montoya-Medina, José E.
|
|
2018
|
|
1 |
p. 167
|
artikel
|
| 27 |
Comparing the Preferences of Patients and the General Public for Treatment Outcomes in Type 2 Diabetes Mellitus
|
Crossnohere, Norah L.
|
|
|
|
1 |
p. 89-100
|
artikel
|
| 28 |
Concordance of Couples’ Prostate Cancer Screening Recommendations from a Decision Analysis
|
Cantor, Scott B.
|
|
2008
|
|
1 |
p. 11-19
|
artikel
|
| 29 |
Conducting Patient-Oriented Research in Low-Income and Middle-Income Countries: A Scoping Review
|
Ibitoye, Bukola Mary
|
|
|
|
1 |
p. 19-29
|
artikel
|
| 30 |
Constructing Health State Descriptions for Low-Risk Thyroid Cancer: Stakeholder Engagement and Formative Qualitative Research
|
Roth, Erin G.
|
|
|
|
1 |
p. 67-76
|
artikel
|
| 31 |
Content Validity for the VVSymQ® Instrument: A New Patient-Reported Outcome Measure for the Assessment of Varicose Veins Symptoms
|
Paty, Jean
|
|
2016
|
|
1 |
p. 51-63
|
artikel
|
| 32 |
Correction to: A Systematic and Critical Review of Discrete Choice Experiments in Asthma and Chronic Obstructive Pulmonary Disease
|
Collacott, Hannah
|
|
|
|
1 |
p. 145
|
artikel
|
| 33 |
Correction to: Comparing the Preferences of Patients and the General Public for Treatment Outcomes in Type 2 Diabetes Mellitus
|
Crossnohere, Norah L.
|
|
|
|
1 |
p. 149
|
artikel
|
| 34 |
Dealing with Discontinuity in Cancer Care Trajectories: Patients’ Solutions
|
Vermond, Debbie
|
|
|
|
1 |
p. 121-130
|
artikel
|
| 35 |
Depressive Symptoms, Cardiac Anxiety, and Fear of Body Sensations in Patients with Non-Cardiac Chest Pain, and Their Relation to Healthcare-Seeking Behavior: A Cross-Sectional Study
|
Mourad, Ghassan
|
|
2015
|
|
1 |
p. 69-77
|
artikel
|
| 36 |
Determining Commonalities in the Experiences of Patients with Rare Diseases: A Qualitative Analysis of US Food and Drug Administration Patient Engagement Sessions
|
Mease, Catherine
|
|
|
|
1 |
p. 25-37
|
artikel
|
| 37 |
Developing a Patient-Directed Policy Framework for Managing Orphan and Ultra-Orphan Drugs Throughout Their Lifecycle
|
Menon, Devidas
|
|
2015
|
|
1 |
p. 103-117
|
artikel
|
| 38 |
Developing Guidance on Ethics for Patient Groups Collecting and Reporting Patient Information for Health Technology Assessments
|
Single, Ann N. V.
|
|
2015
|
|
1 |
p. 1-4
|
artikel
|
| 39 |
Development and Testing of the Insulin Treatment Experience Questionnaire (ITEQ)
|
Moock, Jörn
|
|
2010
|
|
1 |
p. 45-58
|
artikel
|
| 40 |
Development and Use of New Therapeutics for Rare Diseases: Views from Patients, Caregivers, and Advocates
|
Kesselheim, Aaron S.
|
|
2014
|
|
1 |
p. 75-84
|
artikel
|
| 41 |
Development of a Conceptual Model of Chronic Lymphocytic Leukemia to Better Understand the Patient Experience
|
Eek, Daniel
|
|
|
|
1 |
p. 75-87
|
artikel
|
| 42 |
Development of a Discrete-Choice Experiment (DCE) to Elicit Adolescent and Parent Preferences for Hypodontia Treatment
|
Barber, Sophy
|
|
2018
|
|
1 |
p. 137-148
|
artikel
|
| 43 |
Development of an Electronic Daily Uterine Fibroid Symptom Diary
|
Deal, Linda S.
|
|
2011
|
|
1 |
p. 31-44
|
artikel
|
| 44 |
Development of an Item Pool for a Needs-Based Measure of Quality of Life of Carers of a Family Member with Dementia
|
Oyebode, Jan R.
|
|
2018
|
|
1 |
p. 125-136
|
artikel
|
| 45 |
Development of a Novel Tool to Assess the Impact of Itching in Pediatric Cholestasis
|
Kamath, Binita M.
|
|
2017
|
|
1 |
p. 69-82
|
artikel
|
| 46 |
Does EGFR Mutation Type Influence Patient-Reported Outcomes in Patients with Advanced EGFR Mutation-Positive Non-Small-Cell Lung Cancer? Analysis of Two Large, Phase III Studies Comparing Afatinib with Chemotherapy (LUX-Lung 3 and LUX-Lung 6)
|
Wu, Yi-Long
|
|
2017
|
|
1 |
p. 131-141
|
artikel
|
| 47 |
Effects of HIV Medication Complexity and Depression on Adherence to HIV Medication
|
Kumar, Virender
|
|
2010
|
|
1 |
p. 59-69
|
artikel
|
| 48 |
Engaging Patient Advocates and Other Stakeholders to Design Measures of Patient-Centered Communication in Cancer Care
|
Treiman, Katherine
|
|
2016
|
|
1 |
p. 93-103
|
artikel
|
| 49 |
EQ-5D Health Utility Scores: Data from a Comprehensive Canadian Cancer Centre
|
Naik, Hiten
|
|
2016
|
|
1 |
p. 105-115
|
artikel
|
| 50 |
Evaluating the Consistency of Patient Preference Estimates: Systematic Variation in Survival—Adverse Event Trade-Offs in Patients with Cancer or Cardiovascular Disease
|
Marsh, Kevin
|
|
|
|
1 |
p. 69-75
|
artikel
|
| 51 |
Evaluating the European Health Literacy Survey Questionnaire in Patients with Stroke: A Latent Trait Analysis Using Rasch Modeling
|
Huang, Yi-Jing
|
|
2017
|
|
1 |
p. 83-96
|
artikel
|
| 52 |
Evaluation of Patient Satisfaction with Diabetes Management Provided by Clinical Pharmacists in the Patient-Centered Medical Home
|
Shawn McFarland, M.
|
|
2013
|
|
1 |
p. 115-121
|
artikel
|
| 53 |
Family Burden after Severe Brain Injury
|
Mosconi, Paola
|
|
2011
|
|
1 |
p. 55-65
|
artikel
|
| 54 |
FDA Guidance on Selecting, Developing, or Modifying Fit-for-Purpose Clinical Outcome Assessments: Old Wine in a New Bottle?
|
Gnanasakthy, Ari
|
|
|
|
1 |
p. 3-5
|
artikel
|
| 55 |
Fighting to Breathe and Fighting for Health-Related Quality of Life: Measuring the Impact of Being Dependent on Technology for Breathing on the Child and Their Caregiver
|
Verstraete, Janine
|
|
|
|
1 |
p. 65-82
|
artikel
|
| 56 |
Focus Groups in Elderly Ophthalmologic Patients: Setting the Stage for Quantitative Preference Elicitation
|
Danner, Marion
|
|
2015
|
|
1 |
p. 47-57
|
artikel
|
| 57 |
Generating Relevant Information from Patients in the Technology-Enhanced Era of Patient-Focused Drug Development: Opportunities and Challenges
|
Reaney, Matthew
|
|
|
|
1 |
p. 11-16
|
artikel
|
| 58 |
Giving a Voice to Marginalised Groups for Health Care Decision Making
|
De Abreu Lourenço, Richard
|
|
|
|
1 |
p. 5-10
|
artikel
|
| 59 |
Honoring Pioneers in Patient-Centered Outcomes Research
|
Bridges, John F. P.
|
|
2008
|
|
1 |
p. 5-6
|
artikel
|
| 60 |
Hostile Sexist Male Patients and Female Doctors: A Challenging Encounter
|
Klöckner Cronauer, Christina
|
|
2013
|
|
1 |
p. 37-45
|
artikel
|
| 61 |
How Narrative Journalistic Stories Can Communicate the Individual’s Challenges of Daily Living with Amyotrophic Lateral Sclerosis
|
Jeppesen, Jørgen
|
|
2014
|
|
1 |
p. 41-49
|
artikel
|
| 62 |
How Well Do the Generic Multi-attribute Utility Instruments Incorporate Patient and Public Views Into Their Descriptive Systems?
|
Stevens, Katherine J.
|
|
2015
|
|
1 |
p. 5-13
|
artikel
|
| 63 |
Identifying New Zealand Public Preferences for Pharmacist Prescribers in Primary Care: A Discrete Choice Experiment
|
Raghunandan, Rakhee
|
|
|
|
1 |
p. 77-92
|
artikel
|
| 64 |
Identifying the Benefits and Risks of Emerging Treatments for Idiopathic Pulmonary Fibrosis: A Qualitative Study
|
Bridges, John F. P.
|
|
2014
|
|
1 |
p. 85-92
|
artikel
|
| 65 |
If You Want Patients with Knee Osteoarthritis to Exercise, Tell Them about NSAIDs
|
Fraenkel, Liana
|
|
2008
|
|
1 |
p. 21-26
|
artikel
|
| 66 |
Implementing a Health Confidence Tool at Time of Discharge
|
Mattingly, T. Joseph
|
|
2018
|
|
1 |
p. 163-165
|
artikel
|
| 67 |
Improving Interpretation of Evidence Relating to Quality of Life in Health Technology Assessments of Rare Disease Treatments
|
Nicod, Elena
|
|
|
|
1 |
p. 7-17
|
artikel
|
| 68 |
Including Opt-Out Options in Discrete Choice Experiments: Issues to Consider
|
Campbell, Danny
|
|
2018
|
|
1 |
p. 1-14
|
artikel
|
| 69 |
Insulin Administration and the Impacts of Forgetting a Dose
|
Brod, Meryl
|
|
2013
|
|
1 |
p. 63-71
|
artikel
|
| 70 |
Involving Patients in Reducing Decision Uncertainties Around Orphan and Ultra-Orphan Drugs: A Rare Opportunity?
|
Menon, Devidas
|
|
2014
|
|
1 |
p. 29-39
|
artikel
|
| 71 |
Is it Possible to Measure What Truly Matters? The Paradox of Clinical Audit in Developing Continence Service Standards for Older People
|
Brown, Patrick
|
|
2010
|
|
1 |
p. 11-23
|
artikel
|
| 72 |
Item Reduction, Scoring, and First Validation of the ACCEPTance by the Patients of their Treatment (ACCEPT©) Questionnaire
|
Arnould, Benoit
|
|
2016
|
|
1 |
p. 81-92
|
artikel
|
| 73 |
“I Was Trying to Do the Maths”: Exploring the Impact of Risk Communication in Discrete Choice Experiments
|
Vass, Caroline
|
|
2018
|
|
1 |
p. 113-123
|
artikel
|
| 74 |
Letter to the Editor in response to Greidanus et al., June 2020, “The Successful Return-To-Work Questionnaire for Cancer Survivors (I-RTW_CS): Development, Validity and Reproducibility”
|
Kobayashi, Masamitsu
|
|
|
|
1 |
p. 139-140
|
artikel
|
| 75 |
Lillie Shockney
|
Bridges, John F. P.
|
|
2008
|
|
1 |
p. 7-10
|
artikel
|
| 76 |
Making Patient Engagement a Reality
|
Pushparajah, Daphnee S.
|
|
2017
|
|
1 |
p. 1-8
|
artikel
|
| 77 |
Measuring Health-Related Quality of Life in Adolescent Populations: An Empirical Comparison of the CHU9D and the PedsQLTM 4.0 Short Form 15
|
Petersen, Karin Dam
|
|
2017
|
|
1 |
p. 29-37
|
artikel
|
| 78 |
Measuring Pain Catastrophizing and Pain-Related Self-Efficacy: Expert Panels, Focus Groups, and Cognitive Interviews
|
Amtmann, Dagmar
|
|
2017
|
|
1 |
p. 107-117
|
artikel
|
| 79 |
Mobilising the Next Generation of Stated-Preference Studies: the Association of Access Device with Choice Behaviour and Data Quality
|
Vass, Caroline M.
|
|
|
|
1 |
p. 55-63
|
artikel
|
| 80 |
Modeling Organizational Justice Improvements in a Pediatric Health Service
|
Cunningham, Charles E.
|
|
2013
|
|
1 |
p. 45-59
|
artikel
|
| 81 |
Novel Statistical Approach to Determine Inflammatory Bowel Disease: Patients’ Perspectives on Shared Decision Making
|
Siegel, Corey A.
|
|
2015
|
|
1 |
p. 79-89
|
artikel
|
| 82 |
Obesity Modifies the Association of Race/Ethnicity with Medication Adherence in the CARDIA Study
|
Salas, Maribel
|
|
2008
|
|
1 |
p. 41-54
|
artikel
|
| 83 |
Painful Diabetic Peripheral Neuropathy: Results of a Survey Characterizing the Perspectives and Misperceptions of Patients and Healthcare Practitioners
|
Sadosky, Alesia
|
|
2013
|
|
1 |
p. 107-114
|
artikel
|
| 84 |
Patient-Centered Outcome Measures to Assess Functioning in Randomized Controlled Trials of Low-Vision Rehabilitation: A Review
|
Ehrlich, Joshua R.
|
|
2016
|
|
1 |
p. 39-49
|
artikel
|
| 85 |
Patient Evaluation of Satisfaction and Outcomes with an Autoinjector for Self-Administration of Subcutaneous Belimumab in Patients with Systemic Lupus Erythematosus
|
Dashiell-Aje, Ebony
|
|
2017
|
|
1 |
p. 119-129
|
artikel
|
| 86 |
Patient Feedback on Research Studies: How to Interpret Feedback from the ‘Aware’ Patient?
|
Gleason, Kelly T.
|
|
|
|
1 |
p. 147-148
|
artikel
|
| 87 |
Patient Perspectives and Experiences of Preventive Treatments and Self-Injectable Devices for Migraine: A Focus Group Study
|
Seo, Jaein
|
|
|
|
1 |
p. 93-108
|
artikel
|
| 88 |
Patient Perspectives of Dabigatran: Analysis of Online Discussion Forums
|
Vaughan Sarrazin, Mary S.
|
|
2013
|
|
1 |
p. 47-54
|
artikel
|
| 89 |
Patient Preferences for an Oral Anticoagulant after Major Orthopedic Surgery
|
Wilke, Thomas
|
|
2009
|
|
1 |
p. 39-49
|
artikel
|
| 90 |
Patient Preferences for First-Line Oral Treatment for Mild-to-Moderate Ulcerative Colitis
|
Hodgkins, Paul
|
|
2012
|
|
1 |
p. 33-44
|
artikel
|
| 91 |
Patient Preferences for Multi-Cancer Early Detection (MCED) Screening Tests
|
Gelhorn, Heather
|
|
|
|
1 |
p. 43-56
|
artikel
|
| 92 |
Patient Preferences for Oral Anticoagulation Therapy in Atrial Fibrillation: A Systematic Literature Review
|
Wilke, Thomas
|
|
2016
|
|
1 |
p. 17-37
|
artikel
|
| 93 |
Patient Preferences for Pharmacy Services: A Systematic Review of Studies Based on Discrete Choice Experiments
|
Riboulet, Margaux
|
|
|
|
1 |
p. 13-24
|
artikel
|
| 94 |
Patient Preferences for Treatment of Achilles Tendon Pain
|
Sweeting, Kent R.
|
|
2011
|
|
1 |
p. 45-54
|
artikel
|
| 95 |
Patient-Reported Outcome Measures for Chronic Obstructive Pulmonary Disease
|
Jahagirdar, Deepa
|
|
2013
|
|
1 |
p. 11-21
|
artikel
|
| 96 |
Patient-Reported Outcomes in the Phase III BRIGHTE Trial of the HIV-1 Attachment Inhibitor Prodrug Fostemsavir in Heavily Treatment-Experienced Individuals
|
Anderson, Sarah-Jane
|
|
|
|
1 |
p. 131-143
|
artikel
|
| 97 |
Patient-Reported Outcomes, Patient-Reported Information
|
Baldwin, Mike
|
|
2011
|
|
1 |
p. 11-17
|
artikel
|
| 98 |
Patients’ Experience and Perception of Hospital-Treated Clostridium difficile Infections: a Qualitative Study
|
Guillemin, Isabelle
|
|
2014
|
|
1 |
p. 97-105
|
artikel
|
| 99 |
Patients’ Perceptions of Sharing in Decisions
|
Légaré, France
|
|
2012
|
|
1 |
p. 1-19
|
artikel
|
| 100 |
Patient Values and Preferences Surrounding Proton Pump Inhibitor Use: A Scoping Review
|
Thompson, Wade
|
|
2017
|
|
1 |
p. 17-28
|
artikel
|
| 101 |
Peer Support and Mentorship in a US Rare Disease Community: Findings from the Cystinosis in Emerging Adulthood Study
|
Doyle, Maya
|
|
2014
|
|
1 |
p. 65-73
|
artikel
|
| 102 |
Personal Reflections of a Patient Representative in an Appraisal Committee
|
Smit, Cees
|
|
2014
|
|
1 |
p. 5-10
|
artikel
|
| 103 |
Pharmacological Rhythm and Rate Control Treatment for Atrial Fibrillation
|
Edvardsson, Nils
|
|
2010
|
|
1 |
p. 33-43
|
artikel
|
| 104 |
Physical, Social, and Psychological Consequences of Treatment for Hepatitis C
|
Manos, M. Michele
|
|
|
|
1 |
p. 23-34
|
artikel
|
| 105 |
Physical, Social, and Psychological Consequences of Treatment for Hepatitis C
|
Manos, M. Michele
|
|
2013
|
|
1 |
p. 23-34
|
artikel
|
| 106 |
Predicting EuroQoL 5 Dimensions 5 Levels (EQ-5D-5L) Utilities from Older People’s Quality of Life Brief Questionnaire (OPQoL-Brief) Scores
|
Kaambwa, Billingsley
|
|
2017
|
|
1 |
p. 39-54
|
artikel
|
| 107 |
Preferences and Stated Adherence for Antibiotic Treatment of Cystic Fibrosis Pseudomonas Infections
|
Mohamed, Ateesha Farah
|
|
2015
|
|
1 |
p. 59-67
|
artikel
|
| 108 |
Preferences and Willingness to Pay for Medication in Patients with Renal Cell Carcinoma in China: A Discrete-Choice Experiment
|
Ding, Ruilin
|
|
|
|
1 |
p. 97-108
|
artikel
|
| 109 |
Preferences for Monitoring Comprehensive Heart Failure Care: A Latent Class Analysis
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Preferences for Treatments for Major Depressive Disorder: Formative Qualitative Research Using the Patient Experience
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Public and Patient Involvement at the UK National Institute for Health and Clinical Excellence
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Quality of Life in Organ Transplant Recipients Participating in an Online Transplant Community
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Readability and Comprehension of the Geriatric Depression Scale and PROMIS® Physical Function Items in Older African Americans and Latinos
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Re-Engineering the Post-Discharge Appointment Process for General Medicine Patients
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Respondent Understanding in Discrete Choice Experiments: A Scoping Review
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Response to Comment on “The Successful Return-To-Work Questionnaire for Cancer Survivors (I-RTW_CS): Development, Validity and Reproducibility”
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Role Preferences in Medical Decision Making: Relevance and Implications for Health Preference Research
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Segmenting Patients and Physicians Using Preferences from Discrete Choice Experiments
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Serious Choices: A Protocol for an Environmental Scan of Patient Decision Aids for Seriously Ill People at Risk of Death Facing Choices about Life-Sustaining Treatments
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Serious Choices: A Protocol for an Environmental Scan of Patient Decision Aids for Seriously Ill People at Risk of Death Facing Choices about Life-Sustaining Treatments
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Social Stigma in Diabetes
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Social Stigma in Diabetes
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Speaking Out! Qualitative Insights on the Experience of Mothers Who Wanted a Vaginal Birth after a Birth by Cesarean Section
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McGrath, Pam
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Student-Athlete Preferences for Sexual Violence Reporting: A Discrete Choice Experiment
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Symptoms and Concerns Among Children and Young People with Life-Limiting and Life-Threatening Conditions: A Systematic Review Highlighting Meaningful Health Outcomes
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Symptoms and Impacts in Metastatic Castration-Resistant Prostate Cancer: Qualitative Findings from Patient and Physician Interviews
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Testing and Psychometric Validation of a Pediatric Instrument to Self-Assess Symptoms of the Common Cold
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Test-Retest Reliability of an Interactive Voice Response Version of the EQ-5D in a Sample of Cancer Survivors
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The Benefits and Risks of Being a Standardized Patient: A Narrative Review of the Literature
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The Best of Both Worlds: An Example Mixed Methods Approach to Understand Men’s Preferences for the Treatment of Lower Urinary Tract Symptoms
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The Imperative for Patient-Centred Research to Develop Better Quality Services in Rare Diseases
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Towards Personalising the Use of Biologics in Rheumatoid Arthritis: A Discrete Choice Experiment
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Towards Personalizing Treatment for Depression
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Understanding and Assessing the Impact of End-Stage Renal Disease on Quality of Life
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Utility Values for the CP-6D, a Cerebral Palsy-Specific Multi-Attribute Utility Instrument, Using a Discrete Choice Experiment
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Validated Tools to Measure Costs for Patients: A Systematic Review
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Validation of a Patient Satisfaction Scale in Patients Undergoing Bowel Preparation Prior to Colonoscopy
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Validity and Reliability of the Assessment of Quality of Life (AQoL)-8D Multi-Attribute Utility Instrument
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Validity of the Patient Experiences and Satisfaction with Medications (PESaM) Questionnaire
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Video or In-Clinic Consultation? Selection of Attributes as Preparation for a Discrete Choice Experiment Among Key Stakeholders
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Walking Speed and Health‐Related Quality of Life in Multiple Sclerosis
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What Aspects of Quality of Life are Important from Palliative Care Patients’ Perspectives? A Framework Analysis to Inform Preference-Based Measures for Palliative and End-of-Life Settings
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What Author Instructions Do Health Journals Provide for Writing Plain Language Summaries? A Scoping Review
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What Outcomes are Important for Gout Patients? In-Depth Qualitative Research into the Gout Patient Experience to Determine Optimal Endpoints for Evaluating Therapeutic Interventions
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When Time is Not on Your Side
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