Family care-giving and chronic illness: how parents cope with a child with a sickle cell disorder or thalassaemia.
about
Self-care in Patient with Major Thalassemia: A Grounded Theory.Telemedicine: issues and implications.Acceptability of prenatal testing and termination of pregnancy in Pakistan.Minority ethnic families and family-centred care.Haemoglobinopathies and healthcare provision for ethnic minorities.Which psychosocial factors are related to chelation adherence in thalassemia? A systematic review.Interventions for Reducing Parenting Stress in Families With Pediatric Conditions: An Integrative Review."It goes against the grain": A qualitative study of the experiences of parents' administering distressing health-care procedures for their child at home.A new tool for the assessment of satisfaction with iron chelation therapy (ICT-Sat) for patients with β-thalassemia major.Examining the usefulness of a Family Empowerment Program guided by the Illness Beliefs Model for families caring for a child with thalassemia.Psychosocial functioning in adults with beta-thalassaemia major: evidence for resilience.Support Group for Parents Coping with Children with Type 1 Diabetes.A qualitative study exploring the experiences of African-Caribbean informal stroke carers in the UK.Caregiver Burden, Spirituality, and Psychological Well-Being of Parents Having Children with Thalassemia.A family empowerment program for families having children with thalassemia, Thailand.Impact of psychosocial status and disease knowledge on deferoxamine adherence among thalassaemia major adolescents.'Pressure of life': ethnicity as a mediating factor in mid-life and older peoples' experience of high blood pressure.Adolescent boys with sickle cell disease: a qualitative study.Cultural beliefs and coping strategies related to childhood cancer: the perceptions of South Asian immigrant parents in Canada.Do they look after their own? Informal support for South Asian carers.Cultural competency: professional action and South Asian carers.Perceptions of effective self-care support for children and young people with long-term conditions.The impact of regular hospitalization of children living with thalassaemia on their parents in Sri Lanka: a phenomenological study.Carers' representations of affective mental disorders in British Chinese communities.Parent or nurse? The experience of being the parent of a technology-dependent child.Evaluation of a disease-specific self-efficacy instrument in adolescents with sickle cell disease and its relationship to adjustment.Mothers' coping in chronic childhood illness: the effect of presymptomatic diagnosis of vesicoureteric refluxMothers' evolving relationships with doctors and nurses during the chronic childhood illness trajectory
P2860
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P2860
Family care-giving and chronic illness: how parents cope with a child with a sickle cell disorder or thalassaemia.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
2000年學術文章
@zh-hant
name
Family care-giving and chronic ...... cell disorder or thalassaemia.
@en
Family care-giving and chronic ...... cell disorder or thalassaemia.
@nl
type
label
Family care-giving and chronic ...... cell disorder or thalassaemia.
@en
Family care-giving and chronic ...... cell disorder or thalassaemia.
@nl
prefLabel
Family care-giving and chronic ...... cell disorder or thalassaemia.
@en
Family care-giving and chronic ...... cell disorder or thalassaemia.
@nl
P2860
P1476
Family care-giving and chronic ...... cell disorder or thalassaemia.
@en
P2093
Karl Atkin
Waqar I. U. Ahmad
P2860
P356
10.1046/J.1365-2524.2000.00211.X
P577
2000-01-01T00:00:00Z