345 results on '"Grootenhuis, M. A."'
Search Results
2. Support needs of Dutch young adult childhood cancer survivors
3. Efficacy of Op Koers Online, an online group intervention for parents of children with cancer: Results of a randomized controlled trial
4. A vulnerable age group: the impact of cancer on the psychosocial well-being of young adult childhood cancer survivors
5. The impact of maintenance therapy on sleep-wake rhythms and cancer-related fatigue in pediatric acute lymphoblastic leukemia
6. Study protocol: DexaDays-2, hydrocortisone for treatment of dexamethasone-induced neurobehavioral side effects in pediatric leukemia patients: a double-blind placebo controlled randomized intervention study with cross-over design
7. Getting control during follow-up visits: the views and experiences of parents on tumor surveillance after their children have completed therapy for rhabdomyosarcoma or Ewing sarcoma
8. Health-related quality of life of survivors of childhood acute lymphoblastic leukemia: a systematic review
9. Health-related quality of life, developmental milestones, and self-esteem in young adults with bleeding disorders
10. Psychometric properties and norm scores of the sleep self report in Dutch children
11. Patients’ and parents’ views regarding supportive care in childhood cancer
12. Health-related quality of life, developmental milestones, and self-esteem in young adults with bleeding disorders
13. Hearing siblings’ voices: exploring the (online) support needs of siblings of children with a chronic condition
14. Health‐related quality of life of children on treatment for acute lymphoblastic leukemia: A systematic review
15. Dutch norms for the Strengths and Difficulties Questionnaire (SDQ) – parent form for children aged 2–18 years
16. Children with Cancer
17. Support needs of Dutch young adult childhood cancer survivors
18. Anxiety and Depression in Mothers and Fathers of a Chronically Ill Child
19. P06.03 Child, parent, and clinician selection of patient-reported outcome measures to use in pediatric neuro-oncology outpatient follow-up clinics
20. Psychosocial functioning of mothers of boys with haemophilia
21. Social robots in pediatric oncology: opinions of health care providers
22. Reliability, validity and evaluation of the Haemophilia Coping and Perception Test
23. Moderators of the Efficacy of a Psychosocial Group Intervention for Children With Chronic Illness and Their Parents: What Works for Whom?
24. Patient Reported Outcomes in Pediatric Oncology Practice: Suggestions for Future Usage by Parents and Pediatric Oncologists
25. Parental stress and perceived vulnerability at 5 and 10 years after pediatric SCT
26. Parental stress before, during, and after pediatric stem cell transplantation: a review article
27. Remarkable differences: the course of life of young adults with galactosaemia and PKU
28. Op Koers: groepscursussen psycho-educatie en vaardigheidstraining voor chronisch zieke kinderen
29. Sociaal-maatschappelijke gevolgen en kwaliteit van leven in Nederland bij kinderen en jongvolwassenen opgegroeid met een chronische aandoening
30. Omvang en gevolgen van chronische aandoeningen bij kinderen
31. The course of life and quality of life of early and continuously treated Dutch patients with phenylketonuria
32. Opgroeien met een chronische aandoening: levensloop en gevolgen in de jongvolwassenheid
33. Psychosocial Difficulties in Dutch Young Adult Survivors of Childhood Cancer
34. Psychometric Properties of the Pediatric Patient-Reported Outcomes Measurement Information System (PROMIS (R)) Item Banks in a Dutch Clinical Sample of Children with Juvenile Idiopathic Arthritis
35. Positief effect van video-interactiebegeleiding in het kinderziekenhuis
36. Adolescenten met ibd: wat is de rol van coping en is er een relatie met hun kwaliteit van leven?
37. Kwaliteit van leven en coping bij broers en zussen van kinderen met kanker
38. De gezondheidsbeleving van jongvolwassen patiënten met een terminale nierinsufficiëntie sinds de kinderleeftijd is slechts gedeeltelijk gestoord
39. Hoe meet je de kwaliteit van leven van kinderen met een chronische ziekte
40. A new board game to assess coping and perception of children with hemophilia: validation and evaluation: PO 141
41. Patient reported outcomes in clinical hemophilia practice: PB 1.38–4
42. Are survivors of childhood cancer with an unfavourable psychosocial developmental trajectory more likely to apply for disability benefits?
43. Quality of life in young adult survivors of childhood cancer
44. Kwaliteit van leven van Nederlandstalige kinderen met een hiv–infectie of aids
45. Social and emotional adjustment in young survivors of childhood cancer
46. Impaired cognition and schooling in adults with end stage renal disease since childhood. (Original Article)
47. Is illness perception of parents related to severity of disease in children with hemophilia?: PO-MO-209
48. A new tool to assess coping and perception of children with hemophilia: Validation and evaluation: PO-MO-208
49. Adjustment of siblings to childhood cancer: a literature review
50. Health-related quality of life after completion of successful treatment for childhood cancer
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