Results 91 to 100 of about 19,991 (240)

Premonitory Urges and Sensorimotor Processing in Tourette Syndrome

open access: yesBehavioural Neurology, 2013
Most patients with Tourette syndrome report characteristic sensory experiences (premonitory urges) associated with the expression of tic symptoms. Despite the central role of these experiences to the clinical phenomenology of Tourette syndrome, little is
Sangeerthana Rajagopal   +2 more
doaj   +1 more source

Sleep profiles in individuals with rare neurogenetic syndromes

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Aim To characterize sleep profiles in individuals with neurogenetic disorders (NGDs) and examine the contribution of key clinical and psychiatric symptoms to these profiles. Method The parents of 248 individuals (aged 3–45 years) diagnosed with a range of NGDs, including PTEN hamartoma tumor syndrome (n = 111), SYNGAP1‐related intellectual disability ...
Isabella C. Reyes   +7 more
wiley   +1 more source

COMPARISON OF EXECUTIVE FUNCTION IN TOURETTE SYNDROME IN CHILDREN WITH AND WITHOUT ADHD

open access: yesمجله دانشکده پزشکی اصفهان, 2007
Introduction Executive function define as ability to maintain a suitable and gool directed condition for problem solving. The results of previous studies on Tourette syndrome (TS) were contradiction, but the impairment of visual-spatial performance ...
Mojgan Kar Ahmadi, Zahra Shahrivar
doaj  

Intervention outcomes of children with non‐degenerative dystonia and associated hyperkinetic movement disorders: A scoping review

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Abstract Aim To identify the outcomes reported in published studies of intervention approaches used with non‐degenerative childhood hyperkinetic movement disorders, including dystonia, dyskinesia, hypertonia, athetosis, chorea, cerebral palsy, involuntary movement, and kernicterus, and map them to the International Classification of Functioning ...
Hortensia Gimeno   +10 more
wiley   +1 more source

Tourette syndrome research highlights from 2018 [version 1; peer review: 2 approved]

open access: yesF1000Research, 2019
This is the fifth yearly article in the Tourette Syndrome Research Highlights series, summarizing research from 2018 relevant to Tourette syndrome and other tic disorders. The authors briefly summarize reports they consider most important or interesting.
Olivia Rose   +4 more
doaj   +1 more source

Cannabinoids for Tourette's Syndrome

open access: yesCochrane Database of Systematic Reviews, 2009
Gilles de la Tourette Syndrome (GTS) is a developmental neuropsychiatric disorder characterised by the presence of chronic motor and phonic tics. Drugs currently used in the treatment of GTS either lack efficacy or are associated with intolerable side effects.
Adrienne, Curtis   +2 more
openaire   +3 more sources

Genetic testing in paediatric neurological disorders

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
In this study 390 paediatric patients with neurological disorders underwent genetic testing via exome sequencing, commercial panel, in‐house epilepsy, and movement disorder gene panels. Exome sequencing provides the highest diagnostic yield, and severe developmental delay and hypotonia predicted pathogenic variants in the exome sequencing cohort ...
Wafa Bani Uraba   +15 more
wiley   +1 more source

Double‐blind, sham‐controlled, trial of rhythmic 10 Hz median nerve stimulation for the reduction of tics in Tourette syndrome: Analyses of 3‐month follow‐up data for those receiving active stimulation

open access: yesJournal of Neuropsychology, EarlyView.
Abstract Tourette syndrome [TS] is a neurological disorder of childhood onset characterised by the occurrence of tics: repetitive, purposeless movements or vocalisations. Effective treatment for tic disorders is an area of considerable unmet clinical need.
Stephen R. Jackson   +2 more
wiley   +1 more source

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