Stigma in the lives of adolescents with epilepsy: a review of the literature.
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Memory, Executive Skills, and Psychosocial Phenotype in Children with Pharmacoresponsive Epilepsy: Reactivity to InterventionAn Analysis of a Novel, Short-Term Therapeutic Psychoeducational Program for Children and Adolescents with Chronic Neurological Illness and Their Parents; Feasibility and EfficacyContinuing psychosocial care needs in children with new-onset epilepsy and their parentsFear and stigma: the epidemic within the SARS outbreakDiagnosis and management of depression and psychosis in children and adolescents with epilepsy.Psychopathology in children with epilepsy: a meta-analysis.Quality of life for patients with epilepsy is determined by more than seizure control: the role of psychosocial factors.The Stigma Complex.Research implications of the Institute of Medicine Report, Epilepsy Across the Spectrum: Promoting Health and Understanding.Social difficulties in children with epilepsy: review and treatment recommendations.Social stigma in diabetes : a framework to understand a growing problem for an increasing epidemic.Life quality and health in adolescents and emerging adults with epilepsy during the years of transition: a scoping review.Comprehensive evaluation of the psychosocial parameters of epilepsy: a representative population-based study in Prey Veng (Cambodia).Social Behavioral Problems and the Health-Related Quality of Life in Children and Adolescents with Epilepsy.Stigma and Polytherapy: Predictors of Quality of Life in Patients with Epilepsy from South India.Anxiety and Depression in Adolescents With Epilepsy.Clinic-Based Mobile Health Decision Support to Enhance Adult Epilepsy Self-Management: An Intervention Mapping Approach.Patterns of depressive symptoms in epilepsy.Stigma in People With Type 1 or Type 2 Diabetes.Stigma scale of epilepsy: the perception of epilepsy stigma in different cities in Brazil.Measuring Type 1 diabetes stigma: development and validation of the Type 1 Diabetes Stigma Assessment Scale (DSAS-1).Self-reported and parent-reported quality of life of children and adolescents with new-onset epilepsy.Health-related quality of life and self-perceived competence of children assessed before and up to two years after epilepsy surgery.Stigma as a fundamental cause of population health inequalities.Mothers and fathers of children with epilepsy: gender differences in post-traumatic stress symptoms and correlations with mood spectrum symptoms.Advocacy for children with epilepsy: Leveraging the WHA resolution. Advocacy Task Force, Commission of Pediatrics, International League Against Epilepsy.Grupos de Interação Social (GIS): estratégia de empowerment para pessoas com epilepsiaConceptualizing pain-related stigma in adolescent chronic pain: a literature review and preliminary focus group findings
P2860
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P2860
Stigma in the lives of adolescents with epilepsy: a review of the literature.
description
2003 nî lūn-bûn
@nan
2003 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի ապրիլին հրատարակված գիտական հոդված
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2003年の論文
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2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
name
Stigma in the lives of adolescents with epilepsy: a review of the literature.
@ast
Stigma in the lives of adolescents with epilepsy: a review of the literature.
@en
type
label
Stigma in the lives of adolescents with epilepsy: a review of the literature.
@ast
Stigma in the lives of adolescents with epilepsy: a review of the literature.
@en
prefLabel
Stigma in the lives of adolescents with epilepsy: a review of the literature.
@ast
Stigma in the lives of adolescents with epilepsy: a review of the literature.
@en
P1433
P1476
Stigma in the lives of adolescents with epilepsy: a review of the literature.
@en
P2093
Jessica S MacLeod
Joan K Austin
P304
P356
10.1016/S1525-5050(03)00007-6
P577
2003-04-01T00:00:00Z