scholarly journals Effects of age on motor excitability measures from children and adolescents with Tourette syndrome

2016 ◽  
Vol 19 ◽  
pp. 78-86 ◽  
Author(s):  
Sophia E. Pépés ◽  
Amelia Draper ◽  
Georgina M. Jackson ◽  
Stephen R. Jackson
2012 ◽  
Vol 7 (1) ◽  
pp. 29-44 ◽  
Author(s):  
Stephen R. Jackson ◽  
Amy Parkinson ◽  
Valentina Manfredi ◽  
Guy Millon ◽  
Chris Hollis ◽  
...  

2014 ◽  
Vol 72 (12) ◽  
pp. 942-948 ◽  
Author(s):  
Helvio L. Alves ◽  
Elizabeth M. A. B. Quagliato

Tourette syndrome (TS) and tic disorders represent events of familiar magnitude characterized by involuntary movements and/or vocalization. To determine the prevalence of TS/tic disorders we studied a sample of 762 subjects (388 M, 374 F), between 1992 and 1997, age 6 to 43 years old, taken out of a population of 10,155 subjects (4,918 M, 5,237 F; age: 3-56 years old). A structured 4-item questionnaire, direct interview (multistaged), >1 yr follow-up, were used. 9,565 subjects (4,614 M, 4,951 F) sent back the questionnaires, 3,354 of these (1,671 M, 1,683 F) with positive answers to tics. 42 subjects (31 M, 11 F, age: 7-21 years old, mean: 11 years old) met the DSM-III-R criteria. The total minimal prevalence of TS is 0.43%, with a 3:1 ratio male/female. The minimal prevalence of chronic tic disorder is 2.27%. The total minimal prevalence for tic disorders at all is 2.91%. No special education students participation.


Cortex ◽  
2018 ◽  
Vol 109 ◽  
pp. 50-59 ◽  
Author(s):  
Soyoung Kim ◽  
Stephen R. Jackson ◽  
Maddie Groom ◽  
Georgina M. Jackson

2005 ◽  
Vol 20 (6) ◽  
pp. 714-718 ◽  
Author(s):  
Yasser Awaad ◽  
Anne Marie Michon ◽  
Sarah Minarik

2013 ◽  
Vol 27 (1) ◽  
pp. 95-103 ◽  
Author(s):  
Andrea E. Cavanna ◽  
Chiara Luoni ◽  
Claudia Selvini ◽  
Rosanna Blangiardo ◽  
Clare M. Eddy ◽  
...  

Background:Gilles de la Tourette syndrome (GTS) is a chronic childhood-onset neuropsychiatric disorder with a significant impact on patients’ health-related quality of life (HR-QOL). Cavanna et al. (Neurology 2008; 71: 1410–1416) developed and validated the first disease-specific HR-QOL assessment tool for adults with GTS (Gilles de la Tourette Syndrome-Quality of Life Scale, GTS-QOL). This paper presents the translation, adaptation and validation of the GTS-QOL for young Italian patients with GTS.Methods:A three-stage process involving 75 patients with GTS recruited through three Departments of Child and Adolescent Neuropsychiatry in Italy led to the development of a 27-item instrument (Gilles de la Tourette Syndrome-Quality of Life Scale in children and adolescents, C&A-GTS-QOL) for the assessment of HR-QOL through a clinician-rated interview for 6–12 year-olds and a self-report questionnaire for 13–18 year-olds.Results:The C&A-GTS-QOL demonstrated satisfactory scaling assumptions and acceptability. Internal consistency reliability was high (Cronbach’s alpha > 0.7) and validity was supported by interscale correlations (range 0.4–0.7), principal-component factor analysis and correlations with other rating scales and clinical variables.Conclusions:The present version of the C&A-GTS-QOL is the first disease-specific HR-QOL tool for Italian young patients with GTS, satisfying criteria for acceptability, reliability and validity.


2013 ◽  
Vol 9 (1) ◽  
pp. 33-44 ◽  
Author(s):  
Amelia Draper ◽  
Lucinda Jude ◽  
Georgina M. Jackson ◽  
Stephen R. Jackson

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