| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Ability and Willingness to Participate in Dementia Clinical Research: A Qualitative Study
|
Bouranis, Nicole
|
|
|
|
3 |
p. 277-285
|
article
|
| 2 |
A Guide to Measuring and Interpreting Attribute Importance
|
Gonzalez, Juan Marcos
|
|
2019
|
|
3 |
p. 287-295
|
article
|
| 3 |
A Guide to Observable Differences in Stated Preference Evidence
|
Craig, Benjamin Matthew
|
|
|
|
3 |
p. 329-339
|
article
|
| 4 |
A Model of Patient Choice with Mid-Therapy Information
|
Grant, William C.
|
|
2009
|
|
3 |
p. 143-149
|
article
|
| 5 |
A Pilot Study to Identify Areas for Further Improvements in Patient and Public Involvement in Health Technology Assessments for Medicines
|
Messina, Josie
|
|
2012
|
|
3 |
p. 199-211
|
article
|
| 6 |
A Pilot Study to Identify Areas for Further Improvements in Patient and Public Involvement in Health Technology Assessments for Medicines
|
Messina, Josie
|
|
2012
|
|
3 |
p. 199-211
|
article
|
| 7 |
A Qualitative Research for Defining Meaningful Attributes for the Treatment of Inflammatory Bowel Disease from the Patient Perspective
|
Louis, Edouard
|
|
|
|
3 |
p. 317-325
|
article
|
| 8 |
A Qualitative Study of Vulnerable Patient Views of Type 2 Diabetes Consumer Reports
|
Longo, Daniel R.
|
|
2015
|
|
3 |
p. 231-240
|
article
|
| 9 |
Assessing Stated Preferences for Colorectal Cancer Screening: A Critical Systematic Review of Discrete Choice Experiments
|
Wortley, S.
|
|
2014
|
|
3 |
p. 271-282
|
article
|
| 10 |
Association of Pre-Existing Symptoms with Treatment Decisions among Newly Diagnosed Prostate Cancer Patients
|
Zeliadt, Steven B.
|
|
2008
|
|
3 |
p. 189-200
|
article
|
| 11 |
A Standard Set of Value-Based Patient-Centered Outcomes and Measures of Overall Health in Adults
|
Gangannagaripalli, Jaheeda
|
|
|
|
3 |
p. 341-351
|
article
|
| 12 |
A Systematic Review Comparing the Acceptability, Validity and Concordance of Discrete Choice Experiments and Best–Worst Scaling for Eliciting Preferences in Healthcare
|
Whitty, Jennifer A.
|
|
2017
|
|
3 |
p. 301-317
|
article
|
| 13 |
A Systematic Review of Financial Toxicity Among Cancer Survivors: We Can’t Pay the Co-Pay
|
Gordon, Louisa G.
|
|
2016
|
|
3 |
p. 295-309
|
article
|
| 14 |
A Systematic Review of the Use and Quality of Qualitative Methods in Concept Elicitation for Measures with Children and Young People
|
Husbands, Samantha
|
|
|
|
3 |
p. 257-288
|
article
|
| 15 |
Attributes Used for Cancer Screening Discrete Choice Experiments: A Systematic Review
|
Hall, Rebekah
|
|
|
|
3 |
p. 269-285
|
article
|
| 16 |
Behind Closed Doors: What Happens when Patients and Providers Talk about Prostate-Specific Antigen Screening?
|
McCormack, Lauren
|
|
2009
|
|
3 |
p. 191-201
|
article
|
| 17 |
Communicating Uncertainty in Benefits and Harms: A Review of Patient Decision Support Interventions
|
Bansback, Nick
|
|
2016
|
|
3 |
p. 311-319
|
article
|
| 18 |
Comparing Outcomes of a Discrete Choice Experiment and Case 2 Best-Worst Scaling: An Application to Neuromuscular Disease Treatment
|
Soekhai, Vikas
|
|
|
|
3 |
p. 239-253
|
article
|
| 19 |
Comparison of Expected Outcomes between Patients and Neurologists Using Kano’s Methodology in Symptomatic Migraine Treatment
|
Matías-Guiu, Jorge
|
|
2012
|
|
3 |
p. 147-162
|
article
|
| 20 |
Comparison of Expected Outcomes between Patients and Neurologists Using Kano’s Methodology in Symptomatic Migraine Treatment
|
Matías-Guiu, Jorge
|
|
2012
|
|
3 |
p. 147-162
|
article
|
| 21 |
Completing a Questionnaire at Home Prior to Needs Assessment in General Practice: A Qualitative Study of Cancer Patients’ Experience
|
Thayssen, Susanne
|
|
2015
|
|
3 |
p. 223-230
|
article
|
| 22 |
Correction to: Attributes Used for Cancer Screening Discrete Choice Experiments: A Systematic Review
|
Hall, Rebekah
|
|
|
|
3 |
p. 379-381
|
article
|
| 23 |
Correction to: How Does the Public Evaluate Vaccines for Low‑Incidence, Severe‑Outcome Diseases? A General‑Population Choice Experiment
|
Reed Johnson, F.
|
|
|
|
3 |
p. 287
|
article
|
| 24 |
Creation of a Decision Support Tool for Expectant Parents Facing Threatened Periviable Delivery: Application of a User-Centered Design Approach
|
Tucker Edmonds, Brownsyne
|
|
2018
|
|
3 |
p. 327-337
|
article
|
| 25 |
Creation of a Decision Support Tool for Expectant Parents Facing Threatened Periviable Delivery: Application of a User-Centered Design Approach
|
Tucker Edmonds, Brownsyne
|
|
|
|
3 |
p. 327-337
|
article
|
| 26 |
Demonstrating Measurement Equivalence of the Electronic and Paper Formats of the Urticaria Patient Daily Diary in Patients with Chronic Idiopathic Urticaria
|
Flood, Emuella M.
|
|
2013
|
|
3 |
p. 225-231
|
article
|
| 27 |
Development and Content Validity of the Statin Experience Assessment Questionnaire (SEAQ)©
|
Jacobson, Terry A.
|
|
2016
|
|
3 |
p. 321-334
|
article
|
| 28 |
Development and Psychometric Evaluation of the Life Interference Questionnaire for Growth Hormone Deficiency (LIQ-GHD) to Assess Growth Hormone Injection Burden in Children and Adults
|
Turner-Bowker, Diane M.
|
|
|
|
3 |
p. 289-306
|
article
|
| 29 |
Development and Validation of a Functional Health Literacy Test
|
Zhang, Xu-Hao
|
|
2009
|
|
3 |
p. 169-178
|
article
|
| 30 |
Development and Validation of the AFSymp™: An Atrial Fibrillation-Specific Measure of Patient-Reported Symptoms
|
Medin, Jennie
|
|
2014
|
|
3 |
p. 319-327
|
article
|
| 31 |
Development of a Patient-Reported Palliative Care-Specific Health Classification System: The POS-E
|
Dzingina, Mendwas
|
|
2017
|
|
3 |
p. 353-365
|
article
|
| 32 |
Does Diabetes Have an Impact on Health-State Utility? A Study of Asians in Singapore
|
Wang, P.
|
|
2014
|
|
3 |
p. 329-337
|
article
|
| 33 |
Elicitation of Health-Related Utility in Perianal Fistula in Crohn’s Disease
|
Longworth, Louise
|
|
2018
|
|
3 |
p. 339-348
|
article
|
| 34 |
Empirical Investigation of Ranking vs Best–Worst Scaling Generated Preferences for Attributes of Quality of Life: One and the Same or Differentiable?
|
Ratcliffe, Julie
|
|
|
|
3 |
p. 307-315
|
article
|
| 35 |
Engagement of Canadian Patients with Rare Diseases and Their Families in the Lifecycle of Therapy: A Qualitative Study
|
Young, Andrea
|
|
2018
|
|
3 |
p. 353-359
|
article
|
| 36 |
Estimating Preference-Based EQ-5D Health State Utilities or Item Responses from Neuropathic Pain Scores
|
Gu, Ning Yan
|
|
2012
|
|
3 |
p. 185-197
|
article
|
| 37 |
Evaluating Risk Tolerance from a Systematic Review of Preferences: The Case of Patients with Psoriasis
|
Gonzalez, Juan Marcos
|
|
2018
|
|
3 |
p. 285-300
|
article
|
| 38 |
Evaluating the Content of the Communication Items in the CAHPS® Clinician and Group Survey and Supplemental Items with What High-Performing Physicians Say They Do
|
Quigley, Denise D.
|
|
2013
|
|
3 |
p. 169-177
|
article
|
| 39 |
Evaluating the Utility of Existing Patient-Reported Outcome Scales in Novel Patient Populations with Pancreatic Cancer, Lung Cancer, and Myeloproliferative Neoplasms Using Medicare Current Beneficiary Survey Data
|
Ivanova, Jasmina I.
|
|
2013
|
|
3 |
p. 189-200
|
article
|
| 40 |
Examination of the Applicability of the Disabilities of the Arm, Shoulder and Hand (DASH) Questionnaire to Patients with Hand Injuries and Diseases Using Rasch Analysis
|
Braitmayer, Kathrin
|
|
2016
|
|
3 |
p. 367-376
|
article
|
| 41 |
Examining Patients’ Perceptions of Care to Identify Opportunities for Quality Improvement in Psychiatric Inpatient Hospitals
|
Ortiz, Glorimar
|
|
2014
|
|
3 |
p. 301-312
|
article
|
| 42 |
Exit Interviews Examining the Patient Experience in Clinical Trials of Tirzepatide for Treatment of Type 2 Diabetes
|
Matza, Louis S.
|
|
|
|
3 |
p. 367-377
|
article
|
| 43 |
Experience-Based Values: A Framework for Classifying Different Types of Experience in Health Valuation Research
|
Cubi-Molla, Patricia
|
|
2018
|
|
3 |
p. 253-270
|
article
|
| 44 |
Experience of Symptoms and Disease Impact in Patients with Adenomyosis
|
Nelsen, Linda M.
|
|
2017
|
|
3 |
p. 319-328
|
article
|
| 45 |
Exploring the Trade-Off Between Economic and Health Outcomes During a Pandemic: A Discrete Choice Experiment of Lockdown Policies in Australia
|
Manipis, Kathleen
|
|
|
|
3 |
p. 359-371
|
article
|
| 46 |
Factors that Influence Treatment and Non-treatment Decision Making Among Individuals with Inflammatory Bowel Disease: An Integrative Review
|
Kamp, Kendra J.
|
|
2018
|
|
3 |
p. 271-284
|
article
|
| 47 |
Feasibility of a Psychosocial Rehabilitation Intervention to Enhance the Involvement of Relatives in Cancer Rehabilitation: Pilot Study for a Randomized Controlled Trial
|
Ledderer, Loni
|
|
2013
|
|
3 |
p. 201-212
|
article
|
| 48 |
Feasibility of Using Qualitative Interviews to Explore Patients’ Treatment Goals: Experience from Dermatology
|
Blome, Christine
|
|
2015
|
|
3 |
p. 261-269
|
article
|
| 49 |
Finding Out What Matters in Decision-Making Related to Genomics and Personalized Medicine in Pediatric Oncology: Developing Attributes to Include in a Discrete Choice Experiment
|
McCarthy, Maria C.
|
|
|
|
3 |
p. 347-361
|
article
|
| 50 |
Focus Groups to Inform the Development of a Patient-Reported Outcome Measure (PROM) for Temporomandibular Joint Disorders (TMDs)
|
Elstad, Emily
|
|
|
|
3 |
p. 265-276
|
article
|
| 51 |
Gender Differences in the Selection of an Action Plan for Patients with Type 2 Diabetes Mellitus
|
Nuovo, Jim
|
|
2009
|
|
3 |
p. 203-208
|
article
|
| 52 |
Giving Patients’ Preferences a Voice in Medical Treatment Life Cycle: The PREFER Public–Private Project
|
Bekker-Grob, Esther W. de
|
|
2017
|
|
3 |
p. 263-266
|
article
|
| 53 |
Healthcare Experience and their Relationship with Demographic, Disease and Healthcare-Related Variables: A Cross-Sectional Survey of Patients with Chronic Diseases Using the IEXPAC Scale
|
Orozco-Beltrán, Domingo
|
|
2018
|
|
3 |
p. 307-317
|
article
|
| 54 |
High Proportion of Subjective Component to the Disease Activity Score is Associated with Favorable Response to Abatacept in Rheumatoid Arthritis
|
Lee, Jeong Seok
|
|
2018
|
|
3 |
p. 319-326
|
article
|
| 55 |
“If I Wasn’t This Robust”: Patients’ Expectations and Experiences at the Outcome Measures in Rheumatology Conference 2010
|
Wit, Maarten P. T. de
|
|
2013
|
|
3 |
p. 179-187
|
article
|
| 56 |
Impact of Canagliflozin Treatment on Health-Related Quality of Life among People with Type 2 Diabetes Mellitus: A Pooled Analysis of Patient-Reported Outcomes from Randomized Controlled Trials
|
Cai, Jennifer
|
|
2018
|
|
3 |
p. 341-352
|
article
|
| 57 |
Impact of Once-Daily Versus Twice-Daily Dosing Frequency on Adherence to Chronic Medications among Patients with Venous Thromboembolism
|
Laliberté, François
|
|
2013
|
|
3 |
p. 213-224
|
article
|
| 58 |
Improving Outcome-Driven Care in Multiple Myeloma Using Patient-Reported Outcomes: A Qualitative Evaluation Study
|
Bennink, Christine
|
|
|
|
3 |
p. 255-264
|
article
|
| 59 |
Improving the Validity of Stated-Preference Data in Health Research: The Potential of the Time-to-Think Approach
|
Ozdemir, Semra
|
|
2014
|
|
3 |
p. 247-255
|
article
|
| 60 |
Incorporating Quantitative Patient Preference Data into Healthcare Decision Making Processes: Is HTA Falling Behind?
|
Mott, David John
|
|
2018
|
|
3 |
p. 249-252
|
article
|
| 61 |
Initial Validation of a Patient-Reported Measure of Compassion: Determining the Content Validity and Clinical Sensibility among Patients Living with a Life-Limiting and Incurable Illness
|
Sinclair, Shane
|
|
|
|
3 |
p. 327-337
|
article
|
| 62 |
Involving Patients in a Multidisciplinary European Consensus Process and in the Development of a ‘Patient Summary of the Consensus Document for Colon and Rectal Cancer Care’
|
Boelens, Petra G.
|
|
2014
|
|
3 |
p. 261-270
|
article
|
| 63 |
Issues in the Design of Discrete Choice Experiments
|
Norman, Richard
|
|
2018
|
|
3 |
p. 281-285
|
article
|
| 64 |
Making Decisions About Implantable Cardioverter-Defibrillators from Implantation to End of Life: An Integrative Review of Patients’ Perspectives
|
Lewis, Krystina B.
|
|
2014
|
|
3 |
p. 243-260
|
article
|
| 65 |
Mapping Quality of Life (EQ-5D) from DAPsA, Clinical DAPsA and HAQ in Psoriatic Arthritis
|
Mlcoch, Tomas
|
|
2017
|
|
3 |
p. 329-340
|
article
|
| 66 |
Measuring Patient Experience: Concepts and Methods
|
Ahmed, Faraz
|
|
2014
|
|
3 |
p. 235-241
|
article
|
| 67 |
Meeting the Challenges of Intervention Research in Health Science: An Argument for a Multimethod Research Approach
|
Hansen, Helle Ploug
|
|
2015
|
|
3 |
p. 193-200
|
article
|
| 68 |
Moving from Patient Advocacy to Partnership: A Long and Bumpy Road
|
Wong-Rieger, Durhane
|
|
2017
|
|
3 |
p. 271-276
|
article
|
| 69 |
New Insight into the Role of Patients During Medical Appointments: A Synthesis of Three Qualitative Studies
|
Marcinowicz, Ludmila
|
|
2014
|
|
3 |
p. 313-318
|
article
|
| 70 |
“Not Just Little Adults”: Qualitative Methods to Support the Development of Pediatric Patient-Reported Outcomes
|
Arbuckle, Rob
|
|
2013
|
|
3 |
p. 143-159
|
article
|
| 71 |
Not Surprising: Patients Not Engaged and Not Using Public Healthcare Quality Information
|
Wong-Rieger, Durhane
|
|
2016
|
|
3 |
p. 191-192
|
article
|
| 72 |
Our Most Powerful Weapon to Fight COVID-19: Patient Involvement
|
Pitts, Peter J.
|
|
|
|
3 |
p. 255
|
article
|
| 73 |
Patient and Public Involvement in the Development of Healthcare Guidance: An Overview of Current Methods and Future Challenges
|
Rashid, Ahmed
|
|
2016
|
|
3 |
p. 277-282
|
article
|
| 74 |
Patient Involvement in the Design of a Patient-Centered Clinical Trial to Promote Adherence to Supplemental Oxygen Therapy in COPD
|
Holm, Kristen E.
|
|
2015
|
|
3 |
p. 271-279
|
article
|
| 75 |
Patient Perspectives and Experience with Dalfampridine Treatment in Multiple Sclerosis-Related Walking Impairment: The Step Together Program
|
Crayton, Heidi
|
|
2014
|
|
3 |
p. 283-291
|
article
|
| 76 |
Patient Perspectives on the Value of Patient Preference Information in Regulatory Decision Making: A Qualitative Study in Swedish Patients with Rheumatoid Arthritis
|
Bywall, Karin Schölin
|
|
2018
|
|
3 |
p. 297-305
|
article
|
| 77 |
Patient-Reported Outcomes After a Switch to a Single-Tablet Regimen of Rilpivirine, Emtricitabine, and Tenofovir DF in HIV-1-Positive, Virologically Suppressed Individuals: Additional Findings From a Randomized, Open-Label, 48-Week Trial
|
Brunetta, Jason
|
|
2015
|
|
3 |
p. 257-267
|
article
|
| 78 |
Patient-Reported Outcomes in an Observational Cohort of HIV-1-Infected Adults on Darunavir/Cobicistat-Based Regimens: Beyond Viral Suppression
|
Antinori, Andrea
|
|
|
|
3 |
p. 375-387
|
article
|
| 79 |
Patients’ Perceptions of the Interpersonal Sensitivity of Their Healthcare Providers
|
Phillips, Karon L.
|
|
2012
|
|
3 |
p. 175-183
|
article
|
| 80 |
Patients’ Willingness-to-Pay for an Alzheimer’s Disease Medication in Canada
|
Oremus, Mark
|
|
2013
|
|
3 |
p. 161-168
|
article
|
| 81 |
Perceived Benefits and Factors that Influence the Ability to Establish and Maintain Patient Support Groups in Rare Diseases: A Scoping Review
|
Delisle, Vanessa C.
|
|
2016
|
|
3 |
p. 283-293
|
article
|
| 82 |
Perceived Utility of Genomic Sequencing: Qualitative Analysis and Synthesis of a Conceptual Model to Inform Patient-Centered Instrument Development
|
Smith, Hadley Stevens
|
|
|
|
3 |
p. 317-328
|
article
|
| 83 |
Population Preferences for Treatments When Critically Ill: A Discrete Choice Experiment
|
Anstey, Matthew H.
|
|
|
|
3 |
p. 339-346
|
article
|
| 84 |
Practicing Patient-Centered Care
|
Hanyok, Laura A.
|
|
2012
|
|
3 |
p. 141-145
|
article
|
| 85 |
Preferences of Patients with Advanced Colorectal Cancer for Treatment with Oral or Intravenous Chemotherapy
|
Mastroianni, Candida M.
|
|
2008
|
|
3 |
p. 181-187
|
article
|
| 86 |
Psychometric Evaluation of an Inpatient Consumer Survey Measuring Satisfaction with Psychiatric Care
|
Ortiz, Glorimar
|
|
2012
|
|
3 |
p. 163-173
|
article
|
| 87 |
Psychometric Evaluation of an Inpatient Consumer Survey Measuring Satisfaction with Psychiatric Care
|
Ortiz, Glorimar
|
|
2012
|
|
3 |
p. 163-173
|
article
|
| 88 |
Public Involvement in Setting a National Research Agenda
|
Oliver, Sandy
|
|
2009
|
|
3 |
p. 179-190
|
article
|
| 89 |
Public Preferences for Allocating Ventilators in an Intensive Care Unit: A Discrete Choice Experiment
|
Norman, Richard
|
|
|
|
3 |
p. 319-330
|
article
|
| 90 |
Public Preferences for Government Response Policies on Outbreak Control
|
Ozdemir, Semra
|
|
|
|
3 |
p. 347-358
|
article
|
| 91 |
Public Preferences in Priority Setting when Admitting Patients to the ICU During the COVID-19 Crisis: A Pilot Study
|
Gijsbers, Merle
|
|
|
|
3 |
p. 331-338
|
article
|
| 92 |
QALYs for COVID-19: A Comparison of US EQ-5D-5L Value Sets
|
Poteet, Stephen
|
|
|
|
3 |
p. 339-345
|
article
|
| 93 |
Satisfaction with Subcutaneous Golimumab and its Auto-Injector among Rheumatoid Arthritis Patients with Inadequate Response to Adalimumab or Etanercept
|
Dehoratius, Raphael J.
|
|
2018
|
|
3 |
p. 361-369
|
article
|
| 94 |
Seeing is Engaging: Vlogs as a Tool for Patient Engagement
|
Lee, Joy L.
|
|
2017
|
|
3 |
p. 267-270
|
article
|
| 95 |
So You Want to Build Your Disease’s First Online Patient Registry: An Educational Guide for Patient Organizations Based on US and European Experience
|
Wicks, Paul
|
|
|
|
3 |
p. 183-199
|
article
|
| 96 |
Stated and Revealed Preferences for Funding New High-Cost Cancer Drugs: A Critical Review of the Evidence from Patients, the Public and Payers
|
MacLeod, Tatjana E.
|
|
2015
|
|
3 |
p. 201-222
|
article
|
| 97 |
Stated Preference Research in Reproductive and Maternal Healthcare Services in Sub-Saharan Africa: A Systematic Review
|
Erku, Daniel
|
|
|
|
3 |
p. 287-306
|
article
|
| 98 |
Systematic Review of the Effect of a One-Day Versus Seven-Day Recall Duration on Patient Reported Outcome Measures (PROMs)
|
Peasgood, Tessa
|
|
|
|
3 |
p. 201-221
|
article
|
| 99 |
The Economic Impact on Australian Patients with Neuroendocrine Tumours
|
Gordon, Louisa G.
|
|
|
|
3 |
p. 363-373
|
article
|
| 100 |
The Impact of Video-Based Educational Materials with Voiceovers on Preferences for Glucose Monitoring Technology in Patients with Diabetes: A Randomised Study
|
Smith, Ian P.
|
|
|
|
3 |
p. 223-237
|
article
|
| 101 |
The Importance of Disease-Free Survival as a Clinical Trial Endpoint: A Qualitative Study Among Canadian Survivors of Lung Cancer
|
Bever, Andrea
|
|
|
|
3 |
p. 307-316
|
article
|
| 102 |
The Patient Perspective of Diabetes Care: A Systematic Review of Stated Preference Research
|
Arx, Lill-Brith von
|
|
2014
|
|
3 |
p. 283-300
|
article
|
| 103 |
The Pogo-ization of Post-Pandemic Vaccine Policy
|
Pitts, Peter J.
|
|
|
|
3 |
p. 179-181
|
article
|
| 104 |
The Value of Treatment Processes in Germany: A Discrete Choice Experiment on Patient Preferences in Complementary and Conventional Medicine
|
Adam, Daniela
|
|
2018
|
|
3 |
p. 349-360
|
article
|
| 105 |
The Voice of the Patient Methodology: A Novel Mixed-Methods Approach to Identifying Treatment Goals for Men with Prostate Cancer
|
Saigal, Christopher S.
|
|
2016
|
|
3 |
p. 345-352
|
article
|
| 106 |
Time to Embrace a New Patient-Centered Care Rallying Cry: “Why Not?”
|
Frampton, Susan B.
|
|
2014
|
|
3 |
p. 231-233
|
article
|
| 107 |
Towards Patient-Centered Care for Depression
|
Wittink, Marsha N.
|
|
2010
|
|
3 |
p. 145-157
|
article
|
| 108 |
United States COVID-19 Vaccination Preferences (CVP): 2020 Hindsight
|
Craig, Benjamin Matthew
|
|
|
|
3 |
p. 309-318
|
article
|
| 109 |
Unmet Needs Associated with Attention-Deficit/Hyperactivity Disorder in Eight European Countries as Reported by Caregivers and Adolescents: Results from Qualitative Research
|
Sikirica, Vanja
|
|
2014
|
|
3 |
p. 269-281
|
article
|
| 110 |
Use of, Satisfaction with, and Willingness to Switch Prescription and Over-The-Counter Treatments for Chronic Urticaria
|
Stull, Donald E.
|
|
2009
|
|
3 |
p. 151-157
|
article
|
| 111 |
Using Societal Values to Inform Public Health Policy During the COVID-19 Pandemic: The Role of Health Preference Research
|
DiSantostefano, Rachael L.
|
|
|
|
3 |
p. 303-307
|
article
|
| 112 |
Using the Health Utilities Index in Routine Clinical Care: Process, Feasibility, and Acceptability
|
Santana, Maria-Jose
|
|
2009
|
|
3 |
p. 159-167
|
article
|
| 113 |
Validation of the Chinese Version of the Quality of Recovery-15 Score and Its Comparison with the Post-Operative Quality Recovery Scale
|
Bu, Xue-Shan
|
|
2015
|
|
3 |
p. 251-259
|
article
|
| 114 |
Variation in Treatment Priorities for Chronic Hepatitis C: A Latent Class Analysis
|
Fraenkel, Liana
|
|
2015
|
|
3 |
p. 241-249
|
article
|
| 115 |
Variation in Treatment Priorities for Chronic Hepatitis C: A Latent Class Analysis
|
Fraenkel, Liana
|
|
|
|
3 |
p. 241-249
|
article
|
| 116 |
Walking in the Shoes of Patients, Not Just in Their Genes: A Patient-Centered Approach to Genomic Medicine
|
Arora, Neeraj K.
|
|
2014
|
|
3 |
p. 239-245
|
article
|
| 117 |
What’s Important to the Patient? Informational Needs of Patients Making Decisions About Hepatitis C Treatment
|
Evon, Donna M.
|
|
2016
|
|
3 |
p. 335-344
|
article
|
| 118 |
Willingness to Wait for a Vaccine Against COVID-19: Results of a Preference Survey
|
Tervonen, Tommi
|
|
|
|
3 |
p. 373-377
|
article
|
| 119 |
Women’s Willingness to Accept Risks of Medication for Inflammatory Bowel Disease During Pregnancy
|
Kushner, Tatyana
|
|
|
|
3 |
p. 353-365
|
article
|
Journal description