Siblings of children with chronic kidney disease: A qualitative study of everyday life experiences-Reference-Cited by-同舟云学术

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Siblings of children with chronic kidney disease: A qualitative study of everyday life experiences

Published:2021-05-26 Issue:4 Volume:47 Page:242-249
ISSN:1755-6678
Container-title:Journal of Renal Care
language:en
Short-container-title:J Ren Care

Author:

Agerskov Hanne¹²³^ORCID,Thiesson Helle C.¹²,Pedersen Birthe D.²

Affiliation:

1. Department of Nephrology Odense University Hospital Odense Denmark

2. Department of Clinical Research Univerisity of Southern Denmark Odense Denmark

3. Family Focused Healthcare Research Center (FaCe), Department of Clinical Research University of Southern Denmark Odense Denmark

Publisher

Wiley

Subject

Advanced and Specialized Nursing,Nephrology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jorc.12389

Reference26 articles.

1. Everyday life experiences in families with a child with kidney disease

2. The significance of relationships and dynamics in families with a child with end‐stage kidney disease: A qualitative study

3. The effects of chronic renal failure on siblings

4. Range and Heterogeneity of Outcomes in Randomized Trials of Pediatric Chronic Kidney Disease

5. Parenting Stress Among Caregivers of Children With Chronic Illness: A Systematic Review

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The experiences and perceptions of healthy siblings of children with a long-term condition: Umbrella review;Journal of Pediatric Nursing;2024-07

2. Kidney Care in Infancy, Childhood, and Early Adulthood;Renal Nursing;2024-06-28

3. Life outcomes after paediatric kidney transplantation: a qualitative, biographical study in long-term survivors;Archives of Disease in Childhood;2024-01-11

4. Balancing on life's ladder: A meta‐ethnography of the existential experiences of siblings of children with complex care needs;Journal of Advanced Nursing;2023-12-07

5. Living with a rare disease - experiences and needs in pediatric patients and their parents;Orphanet Journal of Rare Diseases;2023-08-11

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