Results 81 to 90 of about 66,189,794 (208)

Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome

open access: yes, 2007
Caspr2 is a member of neurexin superfamily, members of which are transmembrane proteins that mediate cellular interactions in the nervous system. Recently, truncation of the CNTNAP2 gene coding for the Caspr2 protein has been suggested to be associated ...
Bache, I.   +17 more
core   +1 more source

The GTS-QOL (Gilles de la Tourette Syndrome–Quality of Life Scale): cross cultural evaluation of the French version

open access: yes, 2020
All data from the study entitled "The GTS-QOL (Gilles de la Tourette Syndrome–Quality of Life Scale): cross cultural evaluation of the French version".THIS DATASET IS ARCHIVED AT DANS/EASY, BUT NOT ACCESSIBLE HERE.
Rondepierre, F (via Mendeley Data)
core   +2 more sources

Trials of Pharmacological Interventions for Tourette Syndrome: A Systematic Review

open access: yesBehavioural Neurology, 2013
Introduction: Gilles de la Tourette Syndrome (GTS) is a childhood-onset hyperkinetic movement disorder defined by the chronic presence of multiple motor tics and at least one vocal tic and often complicated by co-morbid behavioural problems.
Karen Waldon   +4 more
doaj   +1 more source

Motor Timing in Tourette Syndrome: The Effect of Movement Lateralization and Bimanual Coordination

open access: yesFrontiers in Neurology, 2019
The study of motor timing informs on how temporal information integrates with motor acts. Cortico-basal ganglia and cortico-cerebellar circuits control this integration, whereas transcallosal interhemispheric connectivity modulates finely timed ...
Davide Martino   +13 more
doaj   +1 more source

Developmental Perspective of the Gilles De La Tourette Syndrome

open access: yes, 1983
This paper concerned developmental perspectives of the Gilles de la Tourette Syndrome. Topics addressed included birth, developmental and family histories, and symptom picture. The neglected area of academic achievement was examined.
Robert Kane, Theresa Incagnoli
core   +1 more source

The Gilles de la Tourette syndrome: a principal component factor analytic study of a large pedigree

open access: yes, 2007
Background The genetics and phenotypes of Gilles de la Tourette syndrome are complicated. Once indicated to be inherited as a single major autosomal dominant condition, several areas of interest on many chromosomes and one gene have been identified for ...
Robertson, MM, Cavanna, Andrea; id_orcid
core   +1 more source

Sporadic hyperekplexia plus syndrome

open access: yesJournal of Pediatric Neurosciences, 2017
A disorder of infants and children with pathological startle response, features of other system involvement, falls, and stiffness with retained consciousness.
Sadanandavalli Retnaswami Chandra   +4 more
doaj   +1 more source

The Future of Research in Tourette Syndrome

open access: yesBehavioural Neurology, 2013
Tourette syndrome (TS) is a neurological condition first described by Georges Gilles de la Tourette in 1885. TS was largely thought of as a rare and bizarre condition until the 1960s, when the beneficial effects of neuroleptics on tic symptoms led to an ...
Andrea E. Cavanna   +2 more
doaj   +1 more source

Tetrabenazine-induced oculogyric crisis – a rare complication in the treatment of Gilles de la Tourette syndrome

open access: yesNeuropsychiatric Disease and Treatment, 2016
Piotr Janik,1 Monika Figura1,2 1Department of Neurology, Anna Gostynska Wolski Hospital, 2Department of Neurology, Faculty of Health Sciences, Medical University of Warsaw, Warsaw, Poland Abstract: Tetrabenazine is used in the treatment of chorea ...
Janik P, Figura M
doaj  

TS-EUROTRAIN: A European-wide investigation and training network on the aetiology and pathophysiology of Gilles de la Tourette Syndrome

open access: yesFrontiers in Neuroscience, 2016
Gilles de la Tourette Syndrome (GTS) is characterised by the presence of multiple motor and phonic tics with a fluctuating course of intensity, frequency and severity.
Natalie J Forde   +56 more
doaj   +1 more source

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