Experiences of parents who have children with chronic kidney disease: a systematic review of qualitative studies.
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Psychosocial impact of lymphedema: a systematic review of literature from 2004 to 2011Health care experiences of people with dementia and their caregivers: a meta-ethnographic analysis of qualitative studiesPediatric chronic kidney disease in North CarolinaChanging Needs for Information and Support in an Online System for Parents of Children With Kidney Disease.Using focused ethnography in paediatric settings to explore professionals' and parents' attitudes towards expertise in managing chronic kidney disease stage 3-5An interactive health communication application for supporting parents managing childhood long-term conditions: outcomes of a randomized controlled feasibility trialMultidisciplinary teams, and parents, negotiating common ground in shared-care of children with long-term conditions: a mixed methods study.Distributed expertise: qualitative study of a British network of multidisciplinary teams supporting parents of children with chronic kidney disease.The Child Illness and Resilience Program (CHiRP): a study protocol of a stepped care intervention to improve the resilience and wellbeing of families living with childhood chronic illness.A meta-ethnography of paid dementia care workers' perspectives on their jobs.Fatigue in patients receiving maintenance dialysis: a review of definitions, measures, and contributing factorsStandardised Outcomes in Nephrology-Children and Adolescents (SONG-Kids): a protocol for establishing a core outcome set for children with chronic kidney disease.Health-related quality of life in patients with pediatric onset of end-stage renal disease: state of the art and recommendations for clinical practice.Support interventions for caregivers of people with chronic kidney disease: a systematic review.Psychosocial aspects of children and families of children treated with automated peritoneal dialysis.Constantly responsible, constantly worried, constantly blessed: parenting after pediatric heart transplant.Parents' experiences of living with a child with a long-term condition: a rapid structured review of the literature.The psychosocial impact of completing childhood cancer treatment: a systematic review of the literature.Parental adjustment to the completion of their child's cancer treatment.Psychosocial support for children and families requiring renal replacement therapy.Development of a measure of caregiver burden in paediatric chronic kidney disease: The Paediatric Renal Caregiver Burden Scale.Hemodialysis for infants, children, and adolescents.Dietary adherence in children with chronic kidney disease: a review of the evidence.Information seeking and avoidance throughout the cancer patient journey: two sides of the same coin? A synthesis of qualitative studies.A guide to reading and using systematic reviews of qualitative research.Online Support Program for Parents of Children With a Chronic Kidney Disease Using Intervention Mapping: A Development and Evaluation Protocol."When I had my transplant, I became normal." Adolescent perspectives on life after kidney transplantation.The support needs of parents having a child with a chronic kidney disease: a focus group study.Systematic review of qualitative studies exploring parental experiences in the Neonatal Intensive Care Unit.Moving on: transitioning young people with chronic kidney disease to adult care.Why we need a process on breaking news of Juvenile Idiopathic Arthritis: a mixed methods study.Adherence of pediatric patients to automated peritoneal dialysis.Health-related quality of life functioning over a 2-year period in children with end-stage renal disease.Social impact of dialysis on children and their families."We're not going to say it's suffering; we're going to say it's an experience": The lived experience of maternal caregivers in pediatric kidney transplantation.Children's, parents' and other stakeholders' perspectives on early dietary self-management to delay disease progression of chronic disease in children: a protocol for a mixed studies systematic review with a narrative synthesis.Social, Psychological and Financial Burden on Caregivers of Children with Chronic Illness: A Cross-sectional Study.The experiences of family carers in the delivery of invasive clinical interventions for young people with complex intellectual disabilities: policy disconnect or policy opportunity?Parental perspectives on caring for a child with chronic kidney disease: an in-depth interview study.The Online Parent Information and Support project, meeting parents' information and support needs for home-based management of childhood chronic kidney disease: research protocol.
P2860
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P2860
Experiences of parents who have children with chronic kidney disease: a systematic review of qualitative studies.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on February 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Experiences of parents who hav ...... review of qualitative studies.
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Experiences of parents who hav ...... review of qualitative studies.
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type
label
Experiences of parents who hav ...... review of qualitative studies.
@en
Experiences of parents who hav ...... review of qualitative studies.
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prefLabel
Experiences of parents who hav ...... review of qualitative studies.
@en
Experiences of parents who hav ...... review of qualitative studies.
@nl
P356
P1433
P1476
Experiences of parents who hav ...... review of qualitative studies.
@en
P2093
Alison Lowe
Peter Sainsbury
P304
P356
10.1542/PEDS.2006-3470
P407
P577
2008-02-01T00:00:00Z