18 results on '"Maurice-Stam, Heleen"'
Search Results
2. The impact of clinically relevant health conditions on psychosocial outcomes in survivors of childhood cancer: results of the DCCSS-LATER study
3. Monitoring health related quality of life in survivorship care of young adult survivors of childhood cancer using web-based patient-reported outcome measures: survivors’ and health care practitioners’ perspectives on the KLIK method
4. The Working Mechanisms of Parental Involvement in Interventions for Children with Chronic Illness
5. Psychosocial developmental milestones of young adult survivors of childhood cancer
6. Matching Psychosocial Support Needs of Parents of a Child with a Chronic Illness to a Feasible Intervention
7. Psychosocial developmental trajectory of a cohort of young adults born very preterm and/or with a very low birth weight in the Netherlands
8. First experience with electronic feedback of the Psychosocial Assessment Tool in pediatric cancer care
9. Online cognitive-behavioral based group interventions for adolescents with chronic illness and parents: study protocol of two multicenter randomized controlled trials
10. Psychosocial profile of pediatric brain tumor survivors with neurocognitive complaints
11. Psychometric properties and Dutch norm data of the PedsQL Multidimensional Fatigue Scale for Young Adults
12. Measuring perceived benefit and disease-related burden in young cancer survivors: validation of the Benefit and Burden Scale for Children (BBSC) in the Netherlands
13. Parenting a child with phenylketonuria or galactosemia: implications for health-related quality of life
14. Psychosocial developmental milestones in men with classic galactosemia
15. Quality of life questionnaires for children with cancer and childhood cancer survivors: a review of the development of available measures
16. Wajongers aan het werk: welke factoren kunnen van belang zijn voor arbeidsparticipatie van jonggehandicapten?
17. Implementation of electronic Patient Reported Outcomes in pediatric daily clinical practice: the KLIK experience
18. Parental perceptions of child vulnerability in parents of children with Kawasaki Disease
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