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                             51 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A caregiver educational program improves quality of life and burden for cancer patients and their caregivers: A randomised clinical trial Belgacem, Bénédicte
2013
17 6 p. 870-876
7 p.
artikel
2 A global web-based programme about cancer in language specific for staff, a sick child and their family Nolbris, M. Jenholt
2013
17 6 p. 898-
1 p.
artikel
3 Anxiety, depression and quality of life in Chinese women with breast cancer during and after treatment: A comparative evaluation Ho, Simone S.M.
2013
17 6 p. 877-882
6 p.
artikel
4 Benefit finding in cancer: A review of influencing factors and health outcomes Pascoe, Liz
2013
17 6 p. 760-766
7 p.
artikel
5 Changes in nutritional status and body composition in childhood cancer patients: A prospective cohort study Brinksma, A.
2013
17 6 p. 893-894
2 p.
artikel
6 Collaboration between doctors and nurses in children's cancer care: Insights from a European project Di Giulio, P.
2013
17 6 p. 745-749
5 p.
artikel
7 Differences in morning and evening fatigue in oncology patients and their family caregivers Dhruva, Anand
2013
17 6 p. 841-848
8 p.
artikel
8 Differences in self-reported outcomes of open prostatectomy patients and robotic prostatectomy patients in an international web-based survey O'Shaughnessy, Peter ‘Kevin’
2013
17 6 p. 775-780
6 p.
artikel
9 Editorial Board 2013
17 6 p. i-
1 p.
artikel
10 Effect of psychosocial interventions on outcomes of patients with colorectal cancer: A review of the literature Hoon, Lim Siew
2013
17 6 p. 883-891
9 p.
artikel
11 EORTC QLQ-C30 and FACT-Lym for the assessment of health-related quality of life of newly diagnosed lymphoma patients undergoing chemotherapy Georgakopoulos, Alexandros
2013
17 6 p. 849-855
7 p.
artikel
12 Experiences of siblings of pediatric cancer patients Nonaka, J.
2013
17 6 p. 897-
1 p.
artikel
13 Exploring the relationship between coping, social support and health-related quality of life for prostate cancer survivors: A review of the literature Paterson, Catherine
2013
17 6 p. 750-759
10 p.
artikel
14 Factors related to parents' resilience when their child is suffering from cancer Kawakami, C.
2013
17 6 p. 896-
1 p.
artikel
15 First assessments by specialist cancer nurses in the community: An ethnography Gamlen, Elizabeth
2013
17 6 p. 797-801
5 p.
artikel
16 Food caregivers influence on nutritional intake among admitted haematological cancer patients – A prospective study Lindman, Astrid
2013
17 6 p. 827-834
8 p.
artikel
17 Friendship from the perspective of children with experience of cancer: A focus group study Einberg, E.
2013
17 6 p. 897-
1 p.
artikel
18 ‘Give as much help as you can, but tread carefully’: Grandparenting across the generations when a grandchild is diagnosed with cancer Drew, D.
2013
17 6 p. 896-
1 p.
artikel
19 International collaboration: Working with and through professional groups to inform the science that underpins the care of children and young people Gibson, Faith
2013
17 6 p. 695-696
2 p.
artikel
20 It's time for updating primary nursing in pediatric oncology care: Qualitative study highlighting the perceptions of nurses, physicians and parents Korhonen, Anne
2013
17 6 p. 732-738
7 p.
artikel
21 Loneliness despite the presence of others – Adolescents' experiences of having a parent who becomes ill with cancer Karlsson, Elisabet
2013
17 6 p. 697-703
7 p.
artikel
22 Meanings of being old, living on one's own and suffering from incurable cancer in rural Norway Devik, Siri Andreassen
2013
17 6 p. 781-787
7 p.
artikel
23 Navigation, education and electronic information for adolescents and young adults with cancer: Chemotherapy, calendars, flash drives, and website resources to show you share and care Anderson, P.
2013
17 6 p. 894-
1 p.
artikel
24 Noticeboard 2013
17 6 p. 902-
1 p.
artikel
25 Nursing care for children with Down Syndrome (DS) and leukemia Iida, J.
2013
17 6 p. 894-895
2 p.
artikel
26 Parents' perceptions of their child's symptom burden during and after cancer treatment Hedén, L.
2013
17 6 p. 895-896
2 p.
artikel
27 Patient-reported outcomes collected via smartphone: Adolescent cancer patients' nausea trajectories Baggott, C.
2013
17 6 p. 895-
1 p.
artikel
28 Patients' experiences of supportive care from a long-term perspective after oesophageal cancer surgery – A focus group study Malmström, Marlene
2013
17 6 p. 856-862
7 p.
artikel
29 Performance of the Swedish version of the Revised Piper Fatigue Scale Jakobsson, Sofie
2013
17 6 p. 808-813
6 p.
artikel
30 Physical condition and its relationship to uncertainty of survivors of childhood and adolescence with lower extremity bone tumor in Japan Katsumoto, S.
2013
17 6 p. 895-
1 p.
artikel
31 Procedure of informed assent/consent for clinical trials in pediatric hemato-oncology: The adolescents' and parents' point of view Van de Velde, V.
2013
17 6 p. 892-893
2 p.
artikel
32 Psychological interventions helping pediatric oncology patients cope with medical procedures: A nurse-centered approach Weinstein, Aurélie G.
2013
17 6 p. 726-731
6 p.
artikel
33 Quality of life and symptom prevalence as reported by children with cancer in Lebanon Abu-Saad Huijer, Huda
2013
17 6 p. 704-710
7 p.
artikel
34 Reviewers 2013 2013
17 6 p. 900-901
2 p.
artikel
35 Search for a good fit between nursing practice and electronic nursing records: benefits and limitations of nursing records on a pediatric hemato-oncology ward Willems, E.
2013
17 6 p. 898-899
2 p.
artikel
36 Self-reported psychosocial wellbeing of adolescent childhood cancer survivors Yallop, Kathy
2013
17 6 p. 711-719
9 p.
artikel
37 Social support and quality of life among Chinese breast cancer survivors: Findings from a mixed methods study Cheng, Huilin
2013
17 6 p. 788-796
9 p.
artikel
38 Social support as a moderator between depressive symptoms and quality of life outcomes of breast cancer survivors Huang, Chiung-Yu
2013
17 6 p. 767-774
8 p.
artikel
39 Structure and content in consultations with patients undergoing surgery for colorectal cancer Carlsson, E.
2013
17 6 p. 820-826
7 p.
artikel
40 Suffering indicators in terminally ill children from the parental perspective Montoya-Juárez, R.
2013
17 6 p. 720-725
6 p.
artikel
41 Supportive interventions for parents or caregivers with children diagnosed with cancer: A systematic review Tang, W.P.
2013
17 6 p. 899-
1 p.
artikel
42 Surveillance on central venous catheter complications in paediatric haematology-oncology unit Hung, C.Y.
2013
17 6 p. 897-898
2 p.
artikel
43 Talking with children with cancer about their disease and treatment: An ethnographic study of everyday practice Gibson, F.
2013
17 6 p. 892-
1 p.
artikel
44 The effect of nutrition in cancer management Mngomezulu, G.
2013
17 6 p. 893-
1 p.
artikel
45 The evaluation of an Internet-based TV Conference System (TVCS) to link children undergoing chemotherapy in hospital class and their regular school class Masako, T.
2013
17 6 p. 893-
1 p.
artikel
46 The opinion of Greek parents on the advantages and disadvantages of the outpatient pediatric oncology setting Matziou, Vasiliki
2013
17 6 p. 739-744
6 p.
artikel
47 The Patients Concerns Inventory in head and neck cancer: Comparison between self-completed paper and touch screen versions in the clinic setting Scott, Barry
2013
17 6 p. 863-869
7 p.
artikel
48 The state of dental visit and oral health care in childhood cancer survivors Ito, N.
2013
17 6 p. 898-
1 p.
artikel
49 Translation and linguistic validation of the FACT-EGFRI-18 quality of life instrument from English into Dutch Boers-Doets, Christine B.
2013
17 6 p. 802-807
6 p.
artikel
50 Understanding cancer patients' reflections on good nursing care in light of Antonovsky's theory Kvåle, Kirsti
2013
17 6 p. 814-819
6 p.
artikel
51 Variability in management of implantable ports in oncology outpatients Fernández-de-Maya, José
2013
17 6 p. 835-840
6 p.
artikel
                             51 gevonden resultaten
 
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