Quality of life in mothers and fathers of children treated for acute lymphoblastic leukaemia in Sweden, Finland and Denmark-Reference-Cited by-同舟云学术

Quality of life in mothers and fathers of children treated for acute lymphoblastic leukaemia in Sweden, Finland and Denmark

Published:2022-07-19 Issue:6 Volume:198 Page:1032-1040
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Mogensen Nina¹²^ORCID,Saaranen Ella³,Olsson Erik³,Klug Albertsen Birgitte⁴⁵,Lähteenmäki Päivi M.²⁶,Kreicbergs Ulrika²⁷,Heyman Mats¹²,Harila‐Saari Arja³

Affiliation:

1. Department of Pediatric Oncology Astrid Lindgren Children's Hospital Karolinska University Hospital Stockholm Sweden

2. Department of Women's and Children's Health, Childhood Cancer Research Unit Karolinska Institutet Stockholm Sweden

3. Department of Women's and Children's Health Uppsala University Uppsala Sweden

4. Department of Pediatrics and Adolescent Medicine Aarhus University Hospital Aarhus Denmark

5. Department of Clinical Medicine, Faculty of Medicine University of Aarhus Aarhus Denmark

6. Department of Pediatrics and Adolescent Medicine Turku University Hospital, and Turku University Turku Finland

7. Department of Health Care Sciences, Palliative Research Centre Marie Cederschiöld University Stockholm Sweden

Funder

Barncancerfonden

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.18350

Reference41 articles.

1. Results of NOPHO ALL2008 treatment for patients aged 1–45 years with acute lymphoblastic leukemia

2. Toxicity profile and treatment delays in NOPHO ALL2008-comparing adults and children with Philadelphia chromosome-negative acute lymphoblastic leukemia

3. A systematic review on factors and consequences of parental distress as related to childhood cancer

4. Impact of Caregiver’s Psychological Aspects towards Quality of Life of Children with Acute Lymphoblastic Leukemia (ALL)

5. The impact of caregiver anxiety/depression symptoms and family functioning on child quality of life during pediatric cancer treatment: From diagnosis to 6 months

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