nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Ability and Willingness to Participate in Dementia Clinical Research: A Qualitative Study
|
Bouranis, Nicole |
|
|
|
3 |
p. 277-285 |
artikel |
2 |
A Guide to Measuring and Interpreting Attribute Importance
|
Gonzalez, Juan Marcos |
|
2019 |
|
3 |
p. 287-295 |
artikel |
3 |
A Guide to Observable Differences in Stated Preference Evidence
|
Craig, Benjamin Matthew |
|
|
|
3 |
p. 329-339 |
artikel |
4 |
A Model of Patient Choice with Mid-Therapy Information
|
Grant, William C. |
|
2009 |
|
3 |
p. 143-149 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
8 |
A Qualitative Study of Vulnerable Patient Views of Type 2 Diabetes Consumer Reports
|
Longo, Daniel R. |
|
2015 |
|
3 |
p. 231-240 |
artikel |
9 |
Assessing Stated Preferences for Colorectal Cancer Screening: A Critical Systematic Review of Discrete Choice Experiments
|
Wortley, S. |
|
2014 |
|
3 |
p. 271-282 |
artikel |
10 |
Association of Pre-Existing Symptoms with Treatment Decisions among Newly Diagnosed Prostate Cancer Patients
|
Zeliadt, Steven B. |
|
2008 |
|
3 |
p. 189-200 |
artikel |
11 |
A Standard Set of Value-Based Patient-Centered Outcomes and Measures of Overall Health in Adults
|
Gangannagaripalli, Jaheeda |
|
|
|
3 |
p. 341-351 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
15 |
Attributes Used for Cancer Screening Discrete Choice Experiments: A Systematic Review
|
Hall, Rebekah |
|
|
|
3 |
p. 269-285 |
artikel |
16 |
Behind Closed Doors: What Happens when Patients and Providers Talk about Prostate-Specific Antigen Screening?
|
McCormack, Lauren |
|
2009 |
|
3 |
p. 191-201 |
artikel |
17 |
Communicating Uncertainty in Benefits and Harms: A Review of Patient Decision Support Interventions
|
Bansback, Nick |
|
2016 |
|
3 |
p. 311-319 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
22 |
Correction to: Attributes Used for Cancer Screening Discrete Choice Experiments: A Systematic Review
|
Hall, Rebekah |
|
|
|
3 |
p. 379-381 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
27 |
Development and Content Validity of the Statin Experience Assessment Questionnaire (SEAQ)©
|
Jacobson, Terry A. |
|
2016 |
|
3 |
p. 321-334 |
artikel |
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 |
artikel |
29 |
Development and Validation of a Functional Health Literacy Test
|
Zhang, Xu-Hao |
|
2009 |
|
3 |
p. 169-178 |
artikel |
30 |
Development and Validation of the AFSymp™: An Atrial Fibrillation-Specific Measure of Patient-Reported Symptoms
|
Medin, Jennie |
|
2014 |
|
3 |
p. 319-327 |
artikel |
31 |
Development of a Patient-Reported Palliative Care-Specific Health Classification System: The POS-E
|
Dzingina, Mendwas |
|
2017 |
|
3 |
p. 353-365 |
artikel |
32 |
Does Diabetes Have an Impact on Health-State Utility? A Study of Asians in Singapore
|
Wang, P. |
|
2014 |
|
3 |
p. 329-337 |
artikel |
33 |
Elicitation of Health-Related Utility in Perianal Fistula in Crohn’s Disease
|
Longworth, Louise |
|
2018 |
|
3 |
p. 339-348 |
artikel |
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 |
artikel |
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 |
artikel |
36 |
Estimating Preference-Based EQ-5D Health State Utilities or Item Responses from Neuropathic Pain Scores
|
Gu, Ning Yan |
|
2012 |
|
3 |
p. 185-197 |
artikel |
37 |
Evaluating Risk Tolerance from a Systematic Review of Preferences: The Case of Patients with Psoriasis
|
Gonzalez, Juan Marcos |
|
2018 |
|
3 |
p. 285-300 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
41 |
Examining Patients’ Perceptions of Care to Identify Opportunities for Quality Improvement in Psychiatric Inpatient Hospitals
|
Ortiz, Glorimar |
|
2014 |
|
3 |
p. 301-312 |
artikel |
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 |
artikel |
43 |
Experience-Based Values: A Framework for Classifying Different Types of Experience in Health Valuation Research
|
Cubi-Molla, Patricia |
|
2018 |
|
3 |
p. 253-270 |
artikel |
44 |
Experience of Symptoms and Disease Impact in Patients with Adenomyosis
|
Nelsen, Linda M. |
|
2017 |
|
3 |
p. 319-328 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
48 |
Feasibility of Using Qualitative Interviews to Explore Patients’ Treatment Goals: Experience from Dermatology
|
Blome, Christine |
|
2015 |
|
3 |
p. 261-269 |
artikel |
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 |
artikel |
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 |
artikel |
51 |
Gender Differences in the Selection of an Action Plan for Patients with Type 2 Diabetes Mellitus
|
Nuovo, Jim |
|
2009 |
|
3 |
p. 203-208 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
58 |
Improving Outcome-Driven Care in Multiple Myeloma Using Patient-Reported Outcomes: A Qualitative Evaluation Study
|
Bennink, Christine |
|
|
|
3 |
p. 255-264 |
artikel |
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 |
artikel |
60 |
Incorporating Quantitative Patient Preference Data into Healthcare Decision Making Processes: Is HTA Falling Behind?
|
Mott, David John |
|
2018 |
|
3 |
p. 249-252 |
artikel |
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 |
artikel |
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 |
artikel |
63 |
Issues in the Design of Discrete Choice Experiments
|
Norman, Richard |
|
2018 |
|
3 |
p. 281-285 |
artikel |
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 |
artikel |
65 |
Mapping Quality of Life (EQ-5D) from DAPsA, Clinical DAPsA and HAQ in Psoriatic Arthritis
|
Mlcoch, Tomas |
|
2017 |
|
3 |
p. 329-340 |
artikel |
66 |
Measuring Patient Experience: Concepts and Methods
|
Ahmed, Faraz |
|
2014 |
|
3 |
p. 235-241 |
artikel |
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 |
artikel |
68 |
Moving from Patient Advocacy to Partnership: A Long and Bumpy Road
|
Wong-Rieger, Durhane |
|
2017 |
|
3 |
p. 271-276 |
artikel |
69 |
New Insight into the Role of Patients During Medical Appointments: A Synthesis of Three Qualitative Studies
|
Marcinowicz, Ludmila |
|
2014 |
|
3 |
p. 313-318 |
artikel |
70 |
“Not Just Little Adults”: Qualitative Methods to Support the Development of Pediatric Patient-Reported Outcomes
|
Arbuckle, Rob |
|
2013 |
|
3 |
p. 143-159 |
artikel |
71 |
Not Surprising: Patients Not Engaged and Not Using Public Healthcare Quality Information
|
Wong-Rieger, Durhane |
|
2016 |
|
3 |
p. 191-192 |
artikel |
72 |
Our Most Powerful Weapon to Fight COVID-19: Patient Involvement
|
Pitts, Peter J. |
|
|
|
3 |
p. 255 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
79 |
Patients’ Perceptions of the Interpersonal Sensitivity of Their Healthcare Providers
|
Phillips, Karon L. |
|
2012 |
|
3 |
p. 175-183 |
artikel |
80 |
Patients’ Willingness-to-Pay for an Alzheimer’s Disease Medication in Canada
|
Oremus, Mark |
|
2013 |
|
3 |
p. 161-168 |
artikel |
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 |
artikel |
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 |
artikel |
83 |
Population Preferences for Treatments When Critically Ill: A Discrete Choice Experiment
|
Anstey, Matthew H. |
|
|
|
3 |
p. 339-346 |
artikel |
84 |
Practicing Patient-Centered Care
|
Hanyok, Laura A. |
|
2012 |
|
3 |
p. 141-145 |
artikel |
85 |
Preferences of Patients with Advanced Colorectal Cancer for Treatment with Oral or Intravenous Chemotherapy
|
Mastroianni, Candida M. |
|
2008 |
|
3 |
p. 181-187 |
artikel |
86 |
Psychometric Evaluation of an Inpatient Consumer Survey Measuring Satisfaction with Psychiatric Care
|
Ortiz, Glorimar |
|
2012 |
|
3 |
p. 163-173 |
artikel |
87 |
Psychometric Evaluation of an Inpatient Consumer Survey Measuring Satisfaction with Psychiatric Care
|
Ortiz, Glorimar |
|
2012 |
|
3 |
p. 163-173 |
artikel |
88 |
Public Involvement in Setting a National Research Agenda
|
Oliver, Sandy |
|
2009 |
|
3 |
p. 179-190 |
artikel |
89 |
Public Preferences for Allocating Ventilators in an Intensive Care Unit: A Discrete Choice Experiment
|
Norman, Richard |
|
|
|
3 |
p. 319-330 |
artikel |
90 |
Public Preferences for Government Response Policies on Outbreak Control
|
Ozdemir, Semra |
|
|
|
3 |
p. 347-358 |
artikel |
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 |
artikel |
92 |
QALYs for COVID-19: A Comparison of US EQ-5D-5L Value Sets
|
Poteet, Stephen |
|
|
|
3 |
p. 339-345 |
artikel |
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 |
artikel |
94 |
Seeing is Engaging: Vlogs as a Tool for Patient Engagement
|
Lee, Joy L. |
|
2017 |
|
3 |
p. 267-270 |
artikel |
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 |
artikel |
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 |
artikel |
97 |
Stated Preference Research in Reproductive and Maternal Healthcare Services in Sub-Saharan Africa: A Systematic Review
|
Erku, Daniel |
|
|
|
3 |
p. 287-306 |
artikel |
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 |
artikel |
99 |
The Economic Impact on Australian Patients with Neuroendocrine Tumours
|
Gordon, Louisa G. |
|
|
|
3 |
p. 363-373 |
artikel |
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 |
artikel |
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 |
artikel |
102 |
The Patient Perspective of Diabetes Care: A Systematic Review of Stated Preference Research
|
Arx, Lill-Brith von |
|
2014 |
|
3 |
p. 283-300 |
artikel |
103 |
The Pogo-ization of Post-Pandemic Vaccine Policy
|
Pitts, Peter J. |
|
|
|
3 |
p. 179-181 |
artikel |
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 |
artikel |
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 |
artikel |
106 |
Time to Embrace a New Patient-Centered Care Rallying Cry: “Why Not?”
|
Frampton, Susan B. |
|
2014 |
|
3 |
p. 231-233 |
artikel |
107 |
Towards Patient-Centered Care for Depression
|
Wittink, Marsha N. |
|
2010 |
|
3 |
p. 145-157 |
artikel |
108 |
United States COVID-19 Vaccination Preferences (CVP): 2020 Hindsight
|
Craig, Benjamin Matthew |
|
|
|
3 |
p. 309-318 |
artikel |
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 |
artikel |
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 |
artikel |
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 |
artikel |
112 |
Using the Health Utilities Index in Routine Clinical Care: Process, Feasibility, and Acceptability
|
Santana, Maria-Jose |
|
2009 |
|
3 |
p. 159-167 |
artikel |
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 |
artikel |
114 |
Variation in Treatment Priorities for Chronic Hepatitis C: A Latent Class Analysis
|
Fraenkel, Liana |
|
2015 |
|
3 |
p. 241-249 |
artikel |
115 |
Variation in Treatment Priorities for Chronic Hepatitis C: A Latent Class Analysis
|
Fraenkel, Liana |
|
|
|
3 |
p. 241-249 |
artikel |
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 |
artikel |
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 |
artikel |
118 |
Willingness to Wait for a Vaccine Against COVID-19: Results of a Preference Survey
|
Tervonen, Tommi |
|
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3 |
p. 373-377 |
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119 |
Women’s Willingness to Accept Risks of Medication for Inflammatory Bowel Disease During Pregnancy
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Kushner, Tatyana |
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3 |
p. 353-365 |
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