Parental and child perspectives on adaptation to childhood chronic illness: a qualitative study.
about
The impact of patients' chronic disease on family quality of life: an experience from 26 specialtiesIntegration versus disintegration: a grounded theory study of adolescent and young adult development in the context of perinatally-acquired HIV infectionAutonomic nervous system reactivity: children with and without sickle cell 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.An exploration of parent-child dyadic asthma management influences on quality of life.Positive parenting for healthy living (Triple P) for parents of children with type 1 diabetes: protocol of a randomised controlled trial.Understanding the social networks of parents of children with sickle cell disease.Systematic ethnography of school-age children with bleeding disorders and other chronic illnesses: exploring children's perceptions of partnership roles in family-centred care of their chronic illness.Continued development of the family management style framework.A review of factors associated with mental health in siblings of children with chronic illness.Disorders of sex development: Mothers' experiences of support.Parental cognitive appraisals and coping behaviours following child's epilepsy diagnosis: a qualitative study.About my Child: measuring 'Complexity' in neurodisability. Evidence of reliability and validity.Examining the Roles and Experiences of Fathers of Children With Chronic Kidney DiseaseChinese family management of chronic childhood conditions: a cluster analysis.Growing up with cerebral palsy: perceptions of the influence of family.The impact of chronic physical illness, maternal depressive symptoms, family functioning, and self-esteem on symptoms of anxiety and depression in children.Towards a broader understanding of agency in biomedical ethics.Persistent impact of illness on families of adult survivors of childhood central nervous system tumors: a population-based cohort study.Lived experiences of parents caring for a child with a life-limiting condition in Australia: A qualitative study.Identifying challenges of living with type 1 diabetes: child and youth perspectives.Testing the applicability of the family management style framework to chinese families.Psychotropic drug use as indicator of mental health in adolescents affected by a plexus injury at birth: A large population-based study in Sweden.
P2860
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P2860
Parental and child perspectives on adaptation to childhood chronic illness: a qualitative study.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Parental and child perspective ...... illness: a qualitative study.
@en
Parental and child perspective ...... illness: a qualitative study.
@nl
type
label
Parental and child perspective ...... illness: a qualitative study.
@en
Parental and child perspective ...... illness: a qualitative study.
@nl
prefLabel
Parental and child perspective ...... illness: a qualitative study.
@en
Parental and child perspective ...... illness: a qualitative study.
@nl
P2860
P356
P1476
Parental and child perspective ...... illness: a qualitative study.
@en
P2093
Anne F Gannoni
Rosalyn H Shute
P2860
P356
10.1177/1359104509338432
P577
2009-11-13T00:00:00Z