Transfer as a component of the transition of adolescents with sickle cell disease to adult care: adolescent, adult, and parent perspectives.
about
A biopsychosocial model for the management of patients with sickle-cell disease transitioning to adult medical careAssessing the congruence of transition preparedness as reported by parents and their adolescents with special health care needs.We never thought this would happen: transitioning care of adolescents with perinatally acquired HIV infection from pediatrics to internal medicineFamily and parent influences on pediatric chronic pain: a developmental perspective.Measures of readiness to transition to adult health care for youth with chronic physical health conditions: a systematic review and recommendations for measurement testing and development.Transition from pediatric to adult care for sickle cell disease: results of a survey of pediatric providers.The adolescent with a chronic condition. Part II: healthcare provisionAn exploratory study of future plans and extracurricular activities of transition-age youth and young adults.Transition of care from paediatric to adult rheumatology.Barriers in transition from pediatrics to adult medicine in sickle cell anemia.Exploring Adult Care Experiences and Barriers to Transition in Adult Patients with Sickle Cell DiseaseYoung Adult Perspectives on a Successful Transition from Pediatric to Adult Care in Sickle Cell Disease.Applicability of the SMART Model of Transition Readiness for Sickle-Cell DiseaseTransition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research.Moving young people with sickle cell disease from paediatric to adult services.The role of neuropsychological evaluation in pediatric sickle cell disease.Transition from paediatric to adult care for patients with sickle cell disease.Family caregiving for adults with sickle cell disease and extremely high hospital use.Health-related quality of life and adaptive behaviors of adolescents with sickle cell disease: stress processing moderators.Chronic illness in adolescents: transfer or transition to adult services?Race matters: perceptions of race and racism in a sickle cell center.Identification of risk factors for an unsuccessful transition from pediatric to adult sickle cell disease care.Patient-provider relationships across the transition from pediatric to adult diabetes care: a qualitative study.Informing choice or teaching submission to medical authority: a case study of adolescent transitioning for sickle cell patients.The impact of a managed transition of care upon psychosocial characteristics and patient satisfaction in a cohort of adult survivors of childhood cancer.A clinical tool to measure the components of health-care transition from pediatric care to adult care: the UNC TR(x)ANSITION scale.Evaluation of a disease-specific self-efficacy instrument in adolescents with sickle cell disease and its relationship to adjustment.The Prevocational and Early Employment Needs of Adolescents with Juvenile Idiopathic Arthritis: The Occupational Therapy Perspective
P2860
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P2860
Transfer as a component of the transition of adolescents with sickle cell disease to adult care: adolescent, adult, and parent perspectives.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Transfer as a component of the ...... dult, and parent perspectives.
@en
type
label
Transfer as a component of the ...... dult, and parent perspectives.
@en
prefLabel
Transfer as a component of the ...... dult, and parent perspectives.
@en
P2093
P1476
Transfer as a component of the ...... dult, and parent perspectives.
@en
P2093
P304
P356
10.1016/1054-139X(94)90139-T
P577
1994-11-01T00:00:00Z