Results 71 to 80 of about 1,146,099 (242)

Identification of Two Heritable Cross-Disorder Endophenotypes for Tourette Syndrome [PDF]

, 2017
OBJECTIVE: Phenotypic heterogeneity in Tourette syndrome is partly due to complex genetic relationships among Tourette syndrome, obsessive-compulsive disorder (OCD), and attention deficit hyperactivity disorder (ADHD).
Lee, Paul C, Osiecki, Lisa, Hirschtritt, Matthew E, Dion, Yves, Davis, L. K., Cath, Danielle C, Illmann, C., Grados, M., McGrath, L. M., Scharf, Jeremiah M, Delucchi, Kevin L, Budman, Cathy L, Sandor, P., Pauls, D., Mathews, Carol A, McMahon, William M, Dion, Y., Grados, Marco, Sandor, Paul, Greenberg, Erica, Lyon, G. J., Darrow, Sabrina M, Tourette Syndrome Association International Consortium for Genetics, McMahon, W. M., King, R., Cath, D. C., Delucchi, K. L., Mathews, C. A., Lyon, Gholson J, Osiecki, L., Davis, Lea K, Pauls, David, King, Robert, Greenberg, E., Scharf, J. M., Yu, D., Illmann, Cornelia, Yu, Dongmei, Darrow, S. M., Hirschtritt, M. E., McGrath, Lauren M, Lee, P. C., Budman, C. L.   +42 more
core   +1 more source

Variability of motor imagery in children with cerebral palsy examined using the Hand Laterality Test

Developmental Medicine &Child Neurology, EarlyView.
Variability of motor imagery performance in children with cerebral palsy. Abstract Aim To examine motor imagery performance in children with cerebral palsy (CP) compared to typically developing children and develop a composite motor imagery score to differentiate between the two groups. Method In this cross‐sectional case–control study, 37 participants
Inbar Breuer Asher, Dafna Guttman, Pavel Goldstein, Tal Krasovsky   +3 more
wiley   +1 more source

Premonitory Urges and Sensorimotor Processing in Tourette Syndrome

Behavioural 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, Stefano Seri, Andrea Eugenio Cavanna   +2 more
doaj   +1 more source

Mental health difficulties in cerebral palsy: A qualitative study of young people's and parents' perspectives

Developmental Medicine &Child Neurology, EarlyView.
Abstract Aim To explore the experiences of mental health difficulties and access to mental health support among young people with cerebral palsy (CP). Method We used a qualitative descriptive design. Participants were young people with CP aged 13 to 25 years and parents of children with CP (6–25 years).
Manjula Manikandan, Jennifer Fortune, Jessica Burke, Aisling Walsh, Aoife Twohig, Ian McClelland, Amanda Breen, Meriel Norris, Jennifer M. Ryan, RELATE‐CP study team, Reuel Jalal, Mary Cannon, Kimberley J Smith, Michael Walsh, Ruth Kevlin, Claire Kerr   +15 more
wiley   +1 more source

Self-induced lens subluxation with avulsion of ciliary processes in Tourette Syndrome

American Journal of Ophthalmology Case Reports, 2019
Purpose: To report a case of self-induced eye injury resulting in lens subluxation combined with avulsion of ciliary processes in a patient with Tourette Syndrome.
Carolina L.M. Francisconi, Kamiar Mireskandari, Peter J. Kertes   +2 more
doaj   +1 more source

Descrição atualizada da paralisia cerebral

Developmental Medicine &Child Neurology, EarlyView.
Resumo A paralisia cerebral (PC) é um termo descritivo amplamente utilizado para um espectro de deficiências motoras causadas por lesão ou malformação cerebral não progressiva ocorrida durante as fases iniciais do desenvolvimento. Avanços recentes nas áreas da genética, de pesquisa em inflamação e em neurofisiologia têm refinado a compreensão ...
Bernard Dan, Peter Rosenbaum, Lucinda Carr, Martin Gough, John Coughlan, Nonyelum Nweke   +5 more
wiley   +1 more source

Reliability and stability of cerebral palsy classification scales for individuals with STXBP1‐ and SYNGAP1‐related disorders

Developmental Medicine &Child Neurology, EarlyView.
Aim To determine the interrater reliability and stability of the Gross Motor Function Classification System (GMFCS), Manual Ability Classification System (MACS)/Mini‐MACS, and Communication Function Classification System (CFCS) in individuals with STXBP1‐ and SYNGAP1‐related disorders.
Samuel R. Pierce, Julie M. Orlando, Kristin G. Cunningham, Sarah M. Ruggiero, Michael C. Kaufman, Jillian L. McKee, Ingo Helbig   +6 more
wiley   +1 more source

Evidence for enhanced multi-component behaviour in Tourette syndrome – an EEG study

Scientific Reports, 2017
Evidence suggests that Tourette syndrome is characterized by an increase in dopamine transmission and structural as well as functional changes in fronto-striatal circuits that might lead to enhanced multi-component behaviour integration.
Valerie C. Brandt, Ann-Kathrin Stock, Alexander Münchau, Christian Beste   +3 more
doaj   +1 more source

A contribuição de Charcot para o estudo da síndrome de Tourette Charcot's contribution to the study of Tourette's syndrome

Arquivos de Neuro-Psiquiatria, 2008
Revisamos a história da síndrome de Tourette, com ênfase a contribuição de Jean-Martin Charcot.We review the history of Tourette syndrome, emphasizing the contribution of Jean-Martin Charcot.
Hélio A.G. Teive, Hsin Fen Chien, Renato Puppi Munhoz, Egberto Reis Barbosa   +3 more
doaj   +1 more source

THE GENETICS OF TOURETTE SYNDROME

Neurologic Clinics, 1997
Tourette syndrome has significant genetic determinants. The mode of transmission, while mildly controversial, generally is thought to be due to a single major locus inherited either as an autosomal dominant trait with reduced penetrance, or as a trait with intermediate inheritance in which some heterozygotes manifest the disorder. These is evidence for
J P, Alsobrook, D L, Pauls
openaire   +2 more sources