Results 211 to 220 of about 68,968 (381)

Repeat Expansions with Small TTTCA Insertions in MARCHF6 Cause Familial Myoclonus without Epilepsy

Movement Disorders, EarlyView.
Abstract Background Familial adult myoclonus epilepsy (FAME) is a rare autosomal dominant disorder caused by the same intronic TTTTA/TTTCA repeat expansion in seven distinct genes. TTTTA‐only expansions are benign, whereas those containing TTTCA insertions are pathogenic.
Theresa Kühnel, Elsa Leitão, Renate Lunzer, Fabian Kilpert, Sabine Kaya, Claudia Del Gamba, Kelly Astudillo, Steven Frucht, Marion Simonetta‐Moreau, Eric Bieth, Iris Unterberger, Giulietta Maria Riboldi, Christel Depienne   +12 more
wiley   +1 more source

An adaptive algorithm for fixation, saccade, and glissade detection in eyetracking data

Behavior Research Methods, 2010
M. Nyström, K. Holmqvist
semanticscholar   +1 more source

Nocebo Hypothesis Cognitive Behavioral Therapy for Functional Neurological Symptom Disorder (Motor Type): A Pilot Randomized Controlled Trial

Movement Disorders, EarlyView.
Abstract Background A previous case series showed that Nocebo Hypothesis Cognitive Behavioral Therapy (NH‐CBT) is a promising treatment for Functional Neurological Symptom Disorder (FNSD). Objectives To further evaluate the potential efficacy of NH‐CBT in participants with FNSD (motor type).
Matt Richardson, Maria Kleinstäuber, Dana Wong   +2 more
wiley   +1 more source

Familial congenital saccade initiation failure and isolated cerebellar vermis hypoplasia

, 1998
Christopher M. Harris, P R Hodgkins, A Kriss, W.K. Chong, Dorothy Thompson, Laura E. Mezey, F. Shawkat, D S I. Taylor, John Wilson   +8 more
openalex   +1 more source

“Mini Molar Tooth” Sign in POLR3B‐Associated Cerebellar Ataxia with Hypomyelinating Leukodystrophy

Movement Disorders Clinical Practice, EarlyView.
Luca Marsili, Marcelo A. Kauffman, Blanca Talavera de la Esperanza, Zheming Yu, Donald L. Gilbert, Alberto J. Espay   +5 more
wiley   +1 more source

Head impulse gain and saccade analysis in pontine-cerebellar stroke and vestibular neuritis

Neurology, 2014
Luke Chen, M. Todd, G. M. Halmágyi, S. Aw   +3 more
semanticscholar   +1 more source

Cholinergic System Changes in Dopa‐Unresponsive Freezing of Gait in Parkinson's Disease

Movement Disorders, EarlyView.
Abstract Background Freezing of gait (FoG) is a debilitating mobility disturbance that becomes increasingly resistant to dopaminergic pharmacotherapies with advancing Parkinson's disease (PD). The pathophysiology underlying the response of FoG to dopaminergic treatment is poorly understood.
Kelvin L. Chou, Prabesh Kanel, Miriam van Emde Boas, Stiven Roytman, Giulia Carli, Roger L. Albin, Nicolaas I. Bohnen   +6 more
wiley   +1 more source

Saccade selection in visual search: evidence for spatial frequency specific between-item interactions

, 1999
Iain D. Gilchrist, Charles A. Heywood, John M. Findlay   +2 more
openalex   +1 more source

Tics as a Presenting Symptom in Catatonia

Movement Disorders Clinical Practice, EarlyView.
Lindsey M. Vogt, Nahid Iseyas, Ashley Warnock, Elia Abi‐Jaoude   +3 more
wiley   +1 more source

Definition and Classification of Dystonia

Movement Disorders, EarlyView.
Abstract Dystonia is a movement disorder with varied clinical features and diverse etiologies. Here we present a revision of the 2013 consensus definition and classification of dystonia in light of subsequent publications and experience with its application during the last decade.
Alberto Albanese, Kailash P. Bhatia, Victor S.C. Fung, Mark Hallett, Joseph Jankovic, Christine Klein, Joachim K. Krauss, Anthony E. Lang, Jonathan W. Mink, Sanjay Pandey, Jan K. Teller, Marina A.J. Tijssen, Marie Vidailhet, H.A. Jinnah   +13 more
wiley   +1 more source