A cross-sectional study of health-related quality of life deficits in individuals with comorbid diabetes and cancer
2006; 4: 17
Impact of discussion on preferences elicited in a group setting
2006; 4: 22
Health-related quality of life of irritable bowel syndrome patients in different cultural settings
2006; 4: 21
Sensitivity as outcome measure of androgen replacement: the AMS scale
2006; 4: 23
Factors associated with "Ikigai" among members of a public temporary employment agency for seniors (Silver Human Resources Centre) in Japan; gender differences
2006; 4: 12
The PedsQL™ as a patient-reported outcome in children and adolescents with Attention-Deficit/Hyperactivity Disorder: a population-based study
2006; 4: 26
Psychometric properties of two measures of psychological well-being in adult growth hormone deficiency
2006; 4: 16
Comparison of the SF-6D and the EQ-5D in patients with coronary heart disease
2006; 4: 20
Assessing normative cut points through differential item functioning analysis: An example from the adaptation of the Middlesex Elderly Assessment of Mental State (MEAMS) for use as a cognitive screening test in Turkey
2006; 4: 18
Improvement in quality of life measures in patients with refractory hepatitis C, responding to re-treatment with Pegylated interferon alpha -2b and ribavirin
2006; 4: 30
Quality of life and hormone use: new validation results of MRS scale
2006; 4: 32
Negative impact of chronic obstructive pulmonary disease on the health-related quality of life of patients. Results of the EPIDEPOC study
2006; 4: 31
Prevalence of visual impairment in relation to the number of ophthalmologists in a given area: a nationwide approach
2006; 4: 34
Quality of life in patients with psoriasis
2006; 4: 35
Sexual activity and perceived health among Finnish middle-aged women
2006; 4: 29
Synchrony of change in depressive symptoms, health status, and quality of life in persons with clinical depression
2006; 4: 27
Physical activity is related to quality of life in older adults
2006; 4: 37
Validation of a patient satisfaction questionnaire for anemia treatment, the PSQ-An
2006; 4: 28
Transdermal opioids for cancer pain
2006; 4: 24
Measuring the impact and distress of health problems from the individual's perspective: development of the Perceived Impact of Problem Profile (PIPP)
2006; 4: 36
Validation of an English version of the Child-OIDP index, an oral health-related quality of life measure for children
2006; 4: 38
Parsimonious and efficient assessment of health-related quality of life in osteoarthritis research: validation of the Assessment of Quality of Life (AQoL) instrument
2006; 4: 19
Health related quality of life in Malaysian children with thalassaemia
2006; 4: 39
Interest in healthy living outweighs presumed cultural norms for obesity for Ghanaian women
2006; 4: 44
Psychometric evaluation of the Osteoporosis Patient Treatment Satisfaction Questionnaire (OPSAT-Q™), a novel measure to assess satisfaction with bisphosphonate treatment in postmenopausal women
2006; 4: 42
Assessment of health-related quality of life in arthritis: conceptualization and development of five item banks using item response theory
2006; 4: 33
Health-related quality of life following a clinical weight loss intervention among overweight and obese adults: intervention and 24 month follow-up effects
2006; 4: 43
Do visual analogue scale (VAS) derived standard gamble (SG) utilities agree with Health Utilities Index utilities? A comparison of patient and community preferences for health status in rheumatoid arthritis patients
2006; 4: 25
Japanese version of the Dermatology Life Quality Index: validity and reliability in patients with acne
2006; 4: 46
Quality of life in patients with various Barrett's esophagus associated health states
2006; 4: 45
The OnyCOE-t™ questionnaire: responsiveness and clinical meaningfulness of a patient-reported outcomes questionnaire for toenail onychomycosis
2006; 4: 50
Evaluating preference weights for the Asthma Symptom Utility Index (ASUI) across countries
2006; 4: 51
Minimal changes in health status questionnaires: distinction between minimally detectable change and minimally important change
2006; 4: 54
Decomposition of sources of income-related health inequality applied on SF-36 summary scores: a Danish health survey
2006; 4: 53
Health related quality of life trajectories and predictors following coronary artery bypass surgery
2006; 4: 49
Assessing the construct validity of the Italian version of the EQ-5D: preliminary results from a cross-sectional study in North Italy
2006; 4: 47
Public telesurveillance service for frail elderly living at home, outcomes and cost evolution: a quasi experimental design with two follow-ups
2006; 4: 41
Development of the Well-being questionnaire short-form in Japanese: the W-BQ12
2006; 4: 40
Validation of the Burden Index of Caregivers (BIC), a multidimensional short care burden scale from Japan
2006; 4: 52
Health-related quality of life in food hypersensitive schoolchildren and their families: parents' perceptions
2006; 4: 48
Factors influencing agreement between child self-report and parent proxy-reports on the Pediatric Quality of Life Inventory™ 4.0 (PedsQL™) generic core scales
2006; 4: 58
Hydroxyurea and sickle cell anemia: effect on quality of life
2006; 4: 59
The validity of self-rated health as a measure of health status among young military personnel: evidence from a cross-sectional survey
2006; 4: 57
Cross-diagnostic validity in a generic instrument: an example from the Functional Independence Measure in Scandinavia
2006; 4: 55
Psychometric properties and the prevalence, intensity and causes of oral impacts on daily performance (OIDP) in a population of older Tanzanians
2006; 4: 56
Interpreting the results of patient reported outcome measures in clinical trials: The clinician's perspective
2006; 4: 62
Measuring health-related quality of life in young adolescents: Reliability and validity in the Norwegian version of the Pediatric Quality of Life Inventory™ 4.0 (PedsQL) generic core scales
2006; 4: 61
Responsiveness and minimal important differences for patient reported outcomes
2006; 4: 70
Health-related quality of life in children with newly diagnosed cancer: a one year follow-up study
2006; 4: 63
A comprehensive review of 46 exercise treatment studies in fibromyalgia (1988–2005)
2006; 4: 67
A brief symptom index for advanced renal cell carcinoma
2006; 4: 68
Gender associated differences in determinants of quality of life in patients with COPD: a case series study
2006; 4: 72
The impact of iron overload and its treatment on quality of life: results from a literature review
2006; 4: 73
Cost-utility of routine cataract surgery
2006; 4: 74
How a well-grounded minimal important difference can enhance transparency of labelling claims and improve interpretation of a patient reported outcome measure
2006; 4: 69
Psychometric properties of the Centers for Disease Control and Prevention Health-Related Quality of Life (CDC HRQOL) items in adults with arthritis
2006; 4: 66
The validity and responsiveness of three quality of life measures in the assessment of psoriasis patients: results of a phase II study
2006; 4: 71
The PedsQL™ Present Functioning Visual Analogue Scales: preliminary reliability and validity
2006; 4: 75
Health-related quality of life of Canadian children and youth prenatally exposed to alcohol
2006; 4: 81
The use of the SF-36 questionnaire in adult survivors of childhood cancer: evaluation of data quality, score reliability, and scaling assumptions
2006; 4: 77
Physician-estimated disease severity in patients with chronic heart or lung disease: a cross-sectional analysis
2006; 4: 60
Colonoscopic screening for colorectal cancer improves quality of life measures: a population-based screening study
2006; 4: 82
Positive and negative affect and oral health-related quality of life
2006; 4: 83
Guidance for industry: patient-reported outcome measures: use in medical product development to support labeling claims: draft guidance
2006; 4: 79
A promising method for identifying cross-cultural differences in patient perspective: the use of Internet-based focus groups for content validation of new Patient Reported Outcome assessments
2006; 4: 64
Patient-reported outcomes in a trial of exenatide and insulin glargine for the treatment of type 2 diabetes
2006; 4: 80
Psychometric evaluation and predictive validity of Ryff's psychological well-being items in a UK birth cohort sample of women
2006; 4: 76
Gynecologic oncology patients' satisfaction and symptom severity during palliative chemotherapy
2006; 4: 84
Feedback on the FDA's February 2006 draft guidance on Patient Reported Outcome (PRO) measures from a developer of PRO measures
2006; 4: 78
The FDA guidance for industry on PROs: the point of view of a pharmaceutical company
2006; 4: 85
The impact of xerostomia on oral-health-related quality of life among younger adults
2006; 4: 86
Development and validation of the short version of the Psychological General Well-Being Index (PGWB-S)
2006; 4: 88
Reproducibility and responsiveness of the Symptom Severity Scale and the hand and finger function subscale of the Dutch arthritis impact measurement scales (Dutch-AIMS2-HFF) in primary care patients with wrist or hand problems
2006; 4: 87
Assessing responsiveness of generic and specific health related quality of life measures in heart failure
2006; 4: 89
Measuring health-related quality of life in adolescents and young adults: Swedish normative data for the SF-36 and the HADS, and the influence of age, gender, and method of administration
2006; 4: 91
Evaluation of the Quality of Life in Adult Cancer Survivors (QLACS) scale for long-term cancer survivors in a sample of breast cancer survivors
2006; 4: 92
Are Asians comfortable with discussing death in health valuation studies? A study in multi-ethnic Singapore
2006; 4: 93
Combining scores from different patient reported outcome measures in meta-analyses: when is it justified?
2006; 4: 94
Influence of Interferon beta treatment on quality of life in multiple sclerosis patients
2006; 4: 96
A pilot Internet "Value of Health" Panel: recruitment, participation and compliance
2006; 4: 90
Impact, distress and HRQoL among Malaysian men and women with a mobility impairment
2006; 4: 95
Parent proxy-report of their children's health-related quality of life: an analysis of 13,878 parents' reliability and validity across age subgroups using the PedsQL™ 4.0 Generic Core Scales
2007; 5: 2
How young can children reliably and validly self-report their health-related quality of life?: An analysis of 8,591 children across age subgroups with the PedsQL™ 4.0 Generic Core Scales
2007; 5: 1
Measuring the psychosocial consequences of screening
2007; 5: 3
Quality of life in age-related macular degeneration: a review of the literature
2006; 4: 97
Factor structure of the Singapore English version of the KINDL® children quality of life questionnaire
2007; 5: 4
EuroQol (EQ-5D) measure of quality of life predicts mortality, emergency department utilization, and hospital discharge rates in HIV-infected adults under care
2007; 5: 5
The PedsQL™ as a patient-reported outcome in children and adolescents with fibromyalgia: an analysis of OMERACT domains
2007; 5: 9
Parental perceptions of children's oral health: The Early Childhood Oral Health Impact Scale (ECOHIS)
2007; 5: 6
Examining correlates of treatment satisfaction for injectable insulin in type 2 diabetes: lessons learned from a clinical trial comparing biphasic and basal analogues
2007; 5: 8
Self-report and parent-report of physical and psychosocial well-being in Dutch adolescents with type 1 diabetes in relation to glycemic control
2007; 5: 10
A disease-specific measure of health-related quality of life for use in adults with immune thrombocytopenic purpura: Its development and validation
2007; 5: 11
Translation and validation of non-English versions of the Ankylosing Spondylitis Quality of Life (ASQOL) questionnaire
2007; 5: 7
Assessment of fatigue in chronic disease: a bibliographic study of fatigue measurement scales
2007; 5: 12
Time trends of chest pain symptoms and health related quality of life in coronary artery disease
2007; 5: 13
Assessment of Survivor Concerns (ASC): A newly proposed brief questionnaire
2007; 5: 15
The effect of co-morbidities on health-related quality of life in patients placed on the waiting list for total joint replacement
2007; 5: 16
Theoretical framework and methodological development of common subjective health outcome measures in osteoarthritis: a critical review
2007; 5: 14
Palliative care provision for patients with chronic obstructive pulmonary disease
2007; 5: 17
Health related quality of life and psychosocial function among patients with carcinoid tumours. A longitudinal, prospective, and comparative study
2007; 5: 18