48 results on '"Mattsson, Elisabet"'
Search Results
2. Collaborative Interpretation of Researcher-Generated Photo-Elicitation Findings: Insights From Women With Lived Experience of Homelessness
3. Nurse education about forced migrants with diverse sexual orientations, gender identities, and gender expressions: An exploratory focus group study
4. Health care professionals report positive experience with a breastfeeding training program based on the Baby-Friendly Hospital Initiative for Neonatal Intensive Care
5. Social rights and street-level services for women in homelessness: a qualitative study
6. The relationship between attitudes to homelessness and perceptions of caring behaviours: a cross-sectional study among women experiencing homelessness, nurses and nursing students
7. A comparison of perceptions of caring behaviours among women in homelessness, Registered Nurses and nursing students
8. Peer Support Experienced by Mothers of Children With Congenital Heart Defects in Sweden
9. Experiences of food and mealtime from the perspective of patients with chronic life‐limiting disease: A mixed‐method systematic review
10. “There should be some kind of checklist for the soul”– A qualitative interview study of support needs after end of treatment for gynecologic cancer in young women
11. “Stripped of dignity” – women in homelessness and their perspectives of healthcare services: a qualitative study
12. Developing the Preterm Breastfeeding Attitudes Instrument: A tool for describing attitudes to breastfeeding among health care professionals in neonatal intensive care
13. Caring Behaviors Inventory-24: translation, cross-cultural adaptation and psychometric testing for use in a Swedish context
14. Attitudes Towards Homelessness Inventory--Swedish Version
15. Translation, Cross‐Cultural Adaptation, and Psychometric Analysis of the Attitudes Towards Homelessness Inventory for Use in Sweden
16. Perceptions of care after end-of-treatment among younger women with different gynecologic cancer diagnoses – a qualitative analysis of written responses submitted via a survey
17. Belonging to a community of care: Mothers’ experiences of online peer support groups for parents having lost a child with congenital heart defects
18. Peer support among parents of children with congenital heart defects: A qualitative analysis of written responses submitted via an online survey
19. Being involved in research as a collaborator with experience of a prenatal diagnosis of congenital heart defect in the fetus: a qualitative study
20. Mothers' Adaptation to a Late Preterm Infant When Breastfeeding
21. Homeless persons' experiences of health‐ and social care: A systematic integrative review
22. Written narratives from immigrants following a prenatal diagnosis: qualitative exploratory study
23. Women treated for gynaecological cancer during young adulthood – A mixed-methods study of perceived psychological distress and experiences of support from health care following end-of-treatment
24. Prevalence and predictors of symptoms of anxiety and depression, and comorbid symptoms of distress in parents of childhood cancer survivors and bereaved parents five years after end of treatment or a child’s death
25. Prospective questionnaire study showed that higher self-efficacy predicted longer exclusive breastfeeding by the mothers of late preterm infants
26. Emotional and cognitive experiences during the time of diagnosis and decision-making following a prenatal diagnosis: a qualitative study of males presented with congenital heart defect in the fetus carried by their pregnant partner
27. Early skin-to-skin contact between healthy late preterm infants and their parents: an observational cohort study
28. Quality of Patient Information Websites About Congenital Heart Defects: Mixed-Methods Study of Perspectives Among Individuals With Experience of a Prenatal Diagnosis
29. The emotional process from diagnosis to birth following a prenatal diagnosis of fetal anomaly: A qualitative study of messages in online discussion boards
30. Involvement of persons with lived experience of a prenatal diagnosis of congenital heart defect: an explorative study to gain insights into perspectives on future research
31. Experiences of termination of pregnancy for a fetal anomaly: A qualitative study of virtual community messages
32. Communication of support and critique in Swedish virtual community threads about prenatal diagnoses of fetal anomalies
33. Experiences and preferences of care among Swedish immigrants following a prenatal diagnosis of congenital heart defect in the fetus: a qualitative interview study
34. Experiences of informational needs and received information following a prenatal diagnosis of congenital heart defect
35. Development of health‐related quality of life and symptoms of anxiety and depression among persons diagnosed with cancer during adolescence: a 10‐year follow‐up study
36. Healthy late preterm infants and supplementary artificial milk feeds: Effects on breast feeding and associated clinical parameters
37. Information following a Diagnosis of Congenital Heart Defect: Experiences among Parents to Prenatally Diagnosed Children
38. Content and Quality of Information Websites About Congenital Heart Defects Following a Prenatal Diagnosis
39. Negative and positive consequences of adolescent cancer 10 years after diagnosis: an interview‐based longitudinal study in Sweden
40. The Swedish Version of the Breastfeeding Self-Efficacy Scale–Short Form
41. Cancer during Adolescence: Negative and Positive Consequences Reported Three and Four Years after Diagnosis
42. Mode of administration only has a small effect on data quality and self-reported health status and emotional distress among Swedish adolescents and young adults
43. Aspects of quality of life, anxiety, and depression among persons diagnosed with cancer during adolescence: A long-term follow-up study
44. Are nurses and physicians able to assess which strategies adolescents recently diagnosed with cancer use to cope with disease- and treatment-related distress?
45. Health-related quality of life, anxiety and depression among adolescents and young adults with cancer: A prospective longitudinal study
46. Swedish mothers and fathers of a child diagnosed with cancer A Look at Their Quality of Life
47. Prostate Cancer Registration in Four Swedish Regions 1996: Differences in Incidence, Age Structure and Management
48. Stable isotopic study of the basal type selandian (viborg borehole 5): Preliminary results
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.