about
Ethnic differences in considerations whether or not to participate in prenatal screening for Down syndrome.Ethnic differences in informed decision-making about prenatal screening for Down's syndrome.Information about prenatal screening for Down syndrome: ethnic differences in knowledge.Ethnic differences in determinants of participation and non-participation in prenatal screening for Down syndrome: a theoretical framework.Quality of primary care for resettled refugees in the Netherlands with chronic mental and physical health problems: a cross-sectional analysis of medical records and interview data.Individual differences in the use of the response scale determine valuations of hypothetical health states: an empirical studyA labelled discrete choice experiment adds realism to the choices presented: preferences for surveillance tests for Barrett esophagus.Study protocol: population screening for colorectal cancer by colonoscopy or CT colonography: a randomized controlled trial.Self-rated literacy level does not explain educational differences in health and disease.Well being of obstetric patients on minimal blood transfusions (WOMB trial).Negative health care experiences of immigrant patients: a qualitative study.Effectiveness of a web-based health risk assessment with individually-tailored feedback on lifestyle behaviour: study protocolQuality-of-life effects of prostate-specific antigen screening.A short assessment of health literacy (SAHL) in the Netherlands.Design of a prospective cohort study to assess ethnic inequalities in patient safety in hospital care using mixed methods.Ethnic minority patients not at increased risk of adverse events during hospitalisation in urban hospitals in the Netherlands: results of a prospective observational study.A students' survey of cultural competence as a basis for identifying gaps in the medical curriculum.Course of post-traumatic stress disorder and health care utilisation among resettled refugees in the Netherlands.Reliability and validity of the short form of the child health questionnaire for parents (CHQ-PF28) in large random school based and general population samples.How should health service organizations respond to diversity? A content analysis of six approaches.Different perceptions of the burden of upper GI endoscopy: an empirical study in three patient groupsEvaluation of end-user satisfaction among employees participating in a web-based health risk assessment with tailored feedbackGuidelines for the conduction of follow-up studies measuring injury-related disability.Role of relatives of ethnic minority patients in patient safety in hospital care: a qualitative studyCross-national comparability of burden of disease estimates: the European Disability Weights ProjectCritical review of generic and dermatology-specific health-related quality of life instruments.Has the burden of depression been overestimated?Effect of socioeconomic status on psychosocial problems in 5- to 6-year-old preterm- and term-born children: the ABCD study.Determinants of participation in a web-based health risk assessment and consequences for health promotion programs.Incidence of cervical cancer after several negative smear results by age 50: prospective observational study.Burden of waiting for surveillance CT colonography in patients with screen-detected 6-9 mm polyps.Assessing knowledge and attitudes towards screening among users of Faecal Immunochemical Test (FIT).Ethnic variations in unplanned readmissions and excess length of hospital stay: a nationwide record-linked cohort studyReliability and validity of the Infant and Toddler Quality of Life Questionnaire (ITQOL) in a general population and respiratory disease sample.Knowledge, attitudes and beliefs regarding colorectal cancer screening among ethnic minority groups in the Netherlands - a qualitative study.The effects of screening on health behaviour: a summary of the results of randomized controlled trials.Diabetes self-management in patients with low health literacy: ordering findings from literature in a health literacy framework.Interventions to enhance informed choices among invitees of screening programmes-a systematic review.The Patient Reported Outcomes Following Initial treatment and Long term Evaluation of Survivorship registry: scope, rationale and design of an infrastructure for the study of physical and psychosocial outcomes in cancer survivorship cohorts.Implications of health as 'the ability to adapt and self-manage' for public health policy: a qualitative study.
P50
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P50
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Nederlands onderzoekster (1960-2016)
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1960-09-10T00:00:00Z
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2016-05-09T00:00:00Z
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