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Deirdre O'hare, Valsamma Eapen, Rachel Grove, Edward Helmes, Kerry Mcbain & John Reece. (2017) Youth with Tourette syndrome: Parental perceptions and experiences in the Australian context. Australian Journal of Psychology 69:1, pages 48-57.
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Davide Martino & James LeckmanDenis G. Sukhodolsky, Carla Kalvin, Bekir B. Artukoğlu, Virginia W. Eicher & James F. Leckman. 2022. Tourette Syndrome. Tourette Syndrome
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Jordan F. Garris, David A. Huddleston, Hannah S. Jackson, Paul S. Horn & Donald L. Gilbert. (2020) Implementation of the Mini-Child Tourette Syndrome Impairment Scale: Relationships to Symptom Severity and Treatment Decisions. Journal of Child Neurology 36:4, pages 288-295.
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. (2020) Overcoming the Issue of Language Barriers with Cantonese Speaking Families When Researching the Impact of Developmental Disability.. SunKrist Sociology and Research Journal, pages 1-12.
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Lauren F. Quast, Lindsay D. Rosenthal, Grace K. Cushman, Ana M. Gutiérrez-Colina, Emily I. Braley, Patricia Kardon & Ronald L. Blount. (2019) Relations Between Tic Severity, Emotion Regulation, and Social Outcomes in Youth with Tourette Syndrome. Child Psychiatry & Human Development 51:3, pages 366-376.
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L.B. Dehn, E. Korn-Merker, M. Pfäfflin, U. Ravens-Sieberer & T.W. May. (2014) The Impact on Family Scale: Psychometric analysis of long and short forms in parents of children with epilepsy. Epilepsy & Behavior 32, pages 21-26.
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Rebecca H. Bitsko, Melissa Danielson, Michael King, Susanna N. Visser, Lawrence Scahill & Ruth Perou. (2012) Health Care Needs of Children With Tourette Syndrome. Journal of Child Neurology 28:12, pages 1626-1636.
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L.B. Dehn, E. Korn-Merker, M. Pf?fflin, H. Fischbach, M. Frantz, A. Hauser, U. Ravens-Sieberer & T.W. May. (2013) Erfassung der Belastungen von Eltern anfallskranker KinderAssessment of the burden for parents of epileptic children. Zeitschrift f?r Epileptologie 26:4, pages 214-222.
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V. S. Helgeson, D. Becker, O. Escobar & L. Siminerio. (2012) Families With Children With Diabetes: Implications of Parent Stress for Parent and Child Health. Journal of Pediatric Psychology 37:4, pages 467-478.
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Christine A. Conelea, Douglas W. Woods, Samuel H. Zinner, Cathy Budman, Tanya Murphy, Lawrence D. Scahill, Scott N. Compton & John Walkup. (2010) Exploring the Impact of Chronic Tic Disorders on Youth: Results from the Tourette Syndrome Impact Survey. Child Psychiatry & Human Development 42:2, pages 219-242.
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Michael B. Himle & Douglas W. Woods. (2011) Toward Comprehensive Clinical Care for a Complex Condition: Introduction to the Special Issue on Tourette Syndrome. Journal of Developmental and Physical Disabilities 23:1, pages 1-4.
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Martin E. Franklin, Stephanie H. Best, Michelle A. Wilson, Benjamin Loew & Scott N. Compton. (2011) Habit Reversal Training and Acceptance and Commitment Therapy for Tourette Syndrome: A Pilot Project. Journal of Developmental and Physical Disabilities 23:1, pages 49-60.
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Berney J. Wilkinson, Richard M. Marshall & Brenda Curtwright. (2007) Impact of Tourette’s Disorder on Parent Reported Stress. Journal of Child and Family Studies 17:4, pages 582-598.
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Michael B. Himle, Susanna Chang, Douglas W. Woods, Liviu Bunaciu, Amanda Pearlman, Brian Buzzella & John C. Piacentini. (2007) Evaluating the Contributions of ADHD, OCD, and Tic Symptoms in Predicting Functional Competence in Children with Tic Disorders. Journal of Developmental and Physical Disabilities 19:5, pages 503-512.
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