The adolescent with a chronic condition. Part II: healthcare provision
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Adolescents with congenital heart disease: their opinions about the preparation for transfer to adult care.Improving glycaemic control and life skills in adolescents with type 1 diabetes: a randomised, controlled intervention study using the Guided Self-Determination-Young method in triads of adolescents, parents and health care providers integrated intoWho will care for me next? Transitioning to adulthood with hydrocephalus.The HIV experience: youth identified barriers for transitioning from pediatric to adult care.Adolescent and parent perceptions of patient-centered communication while managing type 1 diabetesFamily-based treatment with transition age youth with anorexia nervosa: a qualitative summary of application in clinical practice.Multiple chronic conditions among outpatient pediatric patients, southeastern Michigan, 2008-2013.Patient-clinician mobile communication: analyzing text messaging between adolescents with asthma and nurse case managers.Digital games for type 1 and type 2 diabetes: underpinning theory with three illustrative examplesAdolescent medicine in paediatric practicePsychosocial aspects of traumatic spinal cord injury with onset during adolescence: a qualitative study.Long-term follow-up of children treated for cancer: why is it necessary, by whom, where and how?Long-term outcome of juvenile idiopathic arthritis following a placebo-controlled trial: sustained benefits of early sulfasalazine treatment.Adolescent's subjective perceptions of chronic disease and related psychosocial factors: highlights from an outpatient context studyParents' experiences of caring for a young person with neurofibromatosis type 1 (NF1): a qualitative study.Pediatric psychosomatic medicine: creating a template for trainingTen years of specialized adult care for phenylketonuria - a single-centre experience.Health professionals' and managers' definitions of developmentally appropriate healthcare for young people: conceptual dimensions and embedded controversies.Ethics in health care services for young persons with neurodevelopmental disabilities: a focus on cerebral palsy.Young adults with paediatric liver disease: future challenges.Problems with oral formulations prescribed to children: a focus group study of healthcare professionals.From controlling to letting go: what are the psychosocial needs of parents of adolescents with a chronic illness?'It is life threatening but I don't mind'. A qualitative study using photo elicitation interviews to explore adolescents' experiences of renal replacement therapies.Knowns and unknowns in the care of pediatric familial hypercholesterolemia.Impact of severe haemophilia A on patients' health status: results from the guardian(™) 1 clinical trial of turoctocog alfa (NovoEight(®) ).The reality of hospitalisation: Stories from family members of their hospital experience for adolescents and young adults living with and dying from cancer.The reality of hospitalisation: stories from family members of their hospital experience for adolescents and young adults living with and dying from cancer.Optimizing outcomes for pediatric recipients.Primary care for children in the 21st century.The triply troubled teenager--chronic conditions associated with fewer protective factors and clustered risk behaviours.Transition of young adults with phenylketonuria from pediatric to adult care.Transplanting the adolescent cystic fibrosis patient: can we do it?The applicability of WHODAS 2.0 in adolescents in China.Relationship between physical disabilities or long-term health problems and health risk behaviors or conditions among US high school students.Guided self-determination-young versus standard care in the treatment of young females with type 1 diabetes: study protocol for a multicentre randomized controlled trial.Experience of Being Young With Psoriasis: Self-Management Support Needs.Evaluation of the Utility of a Transition Workbook in Preparing Adolescent and Young Adult Cancer Survivors for Transition to Adult Services: A Pilot Study.Experiences of attendance at a neuromuscular centre: perceptions of adults with neuromuscular disorders.[Non-adherence to the therapy in Crohn's disease patients: prevalence and risk factors].Transition from pediatric to adult health care: expectations of adolescents with chronic disorders and their parents.
P2860
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P2860
The adolescent with a chronic condition. Part II: healthcare provision
description
2004 nî lūn-bûn
@nan
2004 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
The adolescent with a chronic condition. Part II: healthcare provision
@ast
The adolescent with a chronic condition. Part II: healthcare provision
@en
type
label
The adolescent with a chronic condition. Part II: healthcare provision
@ast
The adolescent with a chronic condition. Part II: healthcare provision
@en
prefLabel
The adolescent with a chronic condition. Part II: healthcare provision
@ast
The adolescent with a chronic condition. Part II: healthcare provision
@en
P2093
P2860
P356
P1476
The adolescent with a chronic condition. Part II: healthcare provision
@en
P2093
P2860
P304
P356
10.1136/ADC.2003.045377
P407
P577
2004-10-01T00:00:00Z