Exploring the impact of chronic tic disorders on youth: results from the Tourette Syndrome Impact Survey. - Wikidata - wikimedia - TriplyDB

Exploring the impact of chronic tic disorders on youth: results from the Tourette Syndrome Impact Survey.

Exploring the impact of chronic tic disorders on youth: results from the Tourette Syndrome Impact Survey.

http://www.wikidata.org/entity/Q34624955

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Sources of Disability in Tourette Syndrome: Children vs. Adults The effects of Gilles de la Tourette syndrome and other chronic tic disorders on quality of life across the lifespan: a systematic review The role of parental perceptions of tic frequency and intensity in predicting tic-related functional impairment in youth with chronic tic disorders Stigma in youth with Tourette's syndrome: a systematic review and synthesis.A Review and Update on Tourette Syndrome: Where Is the Field Headed?European clinical guidelines for Tourette syndrome and other tic disorders. Part I: assessment.Living with tics: reduced impairment and improved quality of life for youth with chronic tic disorders Perceptions of treatment for tics among young people with Tourette syndrome and their parents: a mixed methods study.Bothersome tics in patients with chronic tic disorders: Characteristics and individualized treatment response to behavior therapy.Health care needs of children with Tourette syndrome.SUICIDAL THOUGHTS AND BEHAVIORS IN CHILDREN AND ADOLESCENTS WITH CHRONIC TIC DISORDERS.Factors impacting the quality of peer relationships of youth with Tourette's syndrome.Behavior Therapy for Tic Disorders: An Evidenced-based Review and New Directions for Treatment Research.Clinical Correlates and Predictors of Caregiver Strain in Children with Chronic Tic Disorders.Advances in understanding and treatment of Tourette syndrome.Evidence-based assessment of compulsive skin picking, chronic tic disorders and trichotillomania in children.An Empirical Examination of Symptom Substitution Associated With Behavior Therapy for Tourette's Disorder.Comparing fixed-amount and progressive-amount DRO Schedules for tic suppression in youth with chronic tic disorders.Comorbidities, Social Impact, and Quality of Life in Tourette Syndrome 'Everybody just thinks I'm weird': a qualitative exploration of the psychosocial experiences of adolescents with Tourette syndrome.Suicidal ideation in youth with tic disorders.Health-related quality of life, anxiety and depression in parents of adolescents with Gilles de la Tourette syndrome: a controlled study.The Impact of Tic Severity, Comorbidity and Peer Attachment on Quality of Life Outcomes and Functioning in Tourette's Syndrome: Parental Perspectives.An initial study of family accommodation in children and adolescents with chronic tic disorders.The Differential Impact of Tourette's Syndrome and Comorbid Diagnosis on the Quality of Life and Functioning of Diagnosed Children and Adolescents.The need for a proper definition of a "treatment refractoriness" in tourette syndrome.Peer victimization in youth with Tourette syndrome and other chronic tic disorders.Pilot Testing Behavior Therapy for Chronic Tic Disorders in Neurology and Developmental Pediatrics Clinics.The premonitory urge revisited: An individualized premonitory urge for tics scale.A randomized waitlist-controlled pilot trial of voice over Internet protocol-delivered behavior therapy for youth with chronic tic disorders.Behavior Therapy for Youth With Tourette Disorder.The English Version of the Gilles de la Tourette Syndrome-Quality of Life Scale for Children and Adolescents (C&A-GTS-QOL).Sleep Sufficiency in Pediatric and Adolescent Tourette's Disorder: National Survey of Children's Health.Preliminary evaluation of child self-rating using the Child Tourette Syndrome Impairment Scale.The Subjective Quality of Life in Young People With Tourette Syndrome in China.Impact of Tourette Syndrome on School Measures in a Nationally Representative Sample.Neurocognitive correlates of treatment response in children with Tourette's Disorder.Parenting interventions in tic disorders: an exploration of parents' perspectives.

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Exploring the impact of chronic tic disorders on youth: results from the Tourette Syndrome Impact Survey.

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Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR)

Social and emotional adjustment in children affected with Gilles de la Tourette's syndrome: associations with ADHD and family functioning. Attention Deficit Hyperactivity Disorder

An international perspective on Tourette syndrome: selected findings from 3,500 individuals in 22 countries.

Preschool children with intellectual disability: syndrome specificity, behaviour problems, and maternal well-being.

Tourette syndrome and educational problems in Canada.

The child and adolescent trichotillomania impact project: descriptive psychopathology, comorbidity, functional impairment, and treatment utilization.

The impact of young children with externalizing behaviors on their families.

Syndrome specificity and behavioural disorders in young adults with intellectual disability: cultural differences in family impact.

Exploring the utility of the Spence Children's Anxiety Scales parent- and child-report forms in a North American sample.

Understanding disability in Tourette syndrome.

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