Results 121 to 130 of about 37,346 (289)
Saccades to somatosensory targets. I. behavioral characteristics
, 1996 1. We compared the properties of saccades to somatosensory and visual targets. This comparison provides insight into the translation of sensory signals coding target location in different sensory coordinate frameworks into motor commands of a common ...
D. L. Sparks, J. M. Groh
core +1 more source
Monthly or menstrual? A scoping review of catamenial epilepsy and non‐menstrual seizure rhythms
Epilepsia, EarlyView.Abstract Objective Despite the reported high prevalence of catamenial epilepsy (CE), the condition remains poorly defined, with lack of consensus on what entails a menstrual‐related seizure exacerbation. Emerging evidence of multiday cycles of seizure activity, including about‐monthly cycles, present in both men and women, further confound the ...
Victoria Wong +4 more
wiley +1 more source
Eye tracking disturbances in Schizophrenia
Indian Journal of Ophthalmology, 2000 Purpose: To study the frequency of different types of eye tracking disturbances in schizophrenia. Materials and Methods: Smooth pursuit eye movements were studied by electro-oculography (EOG) in 22 schizophrenic patients (ICD-10 criteria) and 15 age and ...
Sharma Pradeep +2 more
doaj
, 2008 Corrective saccades are small eye movements that redirect gaze whenever the actual eye position differs from the desired eye position. In contrast to various forms of saccades including pro-saccades, recentering-saccades or memory guided saccades ...
Fasler, D. +4 more
core
Multiple memory-guided saccades: movement memory improves the accuracy of memory-guided saccades
, 2008 Multiple Memory Guided Saccades (MMGS) are MGS performed after a Visually Guided Saccade (VGS) toward the same target position. In the MMGS paradigm corrective saccades made after the first MGS proved to be more accurate than in the regular MGS paradigm;
COLNAGHI, SILVIA +16 more
core +1 more source
Kv3.1 activation suppresses provoked and spontaneous seizures in a mouse Dravet syndrome model
Epilepsia, EarlyView.Abstract Objective γ‐Aminobutyric acidergic (GABAergic) parvalbumin‐positive (PV+) interneurons are critical for maintaining cortical inhibitory tone, with their dysfunction predictably leading to epilepsy. Rapid PV+ interneuron firing is essential for their normal function and is maintained in part by potassium voltage‐gated channels.
Sheryl Anne D. Vermudez +11 more
wiley +1 more source
Theory of mind: A cognitive endophenotype of juvenile myoclonic epilepsy?
Epilepsia, EarlyView.Abstract Objective Juvenile myoclonic epilepsy (JME), the most common idiopathic generalized epilepsy, is associated with neuropsychological and psychiatric comorbidities, including social cognition and theory of mind (ToM) deficits. The interplay between clinical features, social cognition, and their neural and genetic substrates remains poorly ...
Bernardo Crespo‐Pimentel +13 more
wiley +1 more source
Validation of the diagnosis of Lennox–Gastaut syndrome: Challenges and lessons learned
Epilepsia, EarlyView.Abstract Objective Lennox–Gastaut Syndrome (LGS) is a severe developmental and epileptic encephalopathy characterized by multiple seizure types, cognitive impairment, and distinct electroencephalographic (EEG) findings. However, evolving diagnostic criteria, heterogeneous clinical features, and inconsistent electronic health record (EHR) documentation ...
Nicole Villalba +11 more
wiley +1 more source
Epilepsy syndromes classification
Epilepsia Open, EarlyView.Abstract Epilepsy syndromes are distinct electroclinical entities which have been recently defined by the International League Against Epilepsy Nosology and Definitions Task Force. Each syndrome is associated with “a characteristic cluster of clinical and EEG features, often supported by specific etiologic findings”.
Elaine C. Wirrell +4 more
wiley +1 more source