Results 151 to 160 of about 26,823 (310)

Impact of post stroke fatigue on saccadic eye movement control and learning through inflammatory mechanisms

Scientific Reports
This study aimed to (1) examine the impact of post-stroke fatigue (PSF) on saccadic control, (2) assess the effect of PSF on saccade adaptation, and (3) explore the correlation between serum levels of interleukin-6 (IL-6) and high-sensitivity C-reactive ...
Akram Jamali, Tourandokht Baluchnejadmojarad, Hajar Mehdizadeh, Seyede Zohreh Jazaeri, Soheila Fallah, Ghorban Taghizadeh   +5 more
doaj   +1 more source

The Spectrum of Abnormal Tongue Movements: Review of Phenomenology, Etiology, and Differential Diagnosis

Movement Disorders Clinical Practice, EarlyView.
ABSTRACT Background Classifying abnormal tongue movements is challenging due to their varied presentations and limited visibility compared to other body parts. Accurate identification of the phenomenology guides physical examination and can point to specific diagnoses.
Nathaniel Bendahan, Seyed‐Mohammad Fereshtehnejad, Christos Ganos, Emily Swinkin, Anthony E. Lang   +4 more
wiley   +1 more source

Convergence Deficits in Myoclonus‐Dystonia Point to Cerebellar Impairment

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Myoclonus‐dystonia (M‐D) is a monogenic movement disorder, with proposed cerebellar dysfunction. Vergence eye movement deficits, characteristics of degenerative cerebellar disease, have not been studied in M‐D. Cerebellar transcranial alternating current stimulation (tACS) is considered a potential therapeutic approach.
Skadi Gerkensmeier, Christina Bolte, Jan‐Ole Radecke, Feline Hamami, Andreas Sprenger, Christoph Helmchen, Robert Chen, Marcus Callister, Talyta Cortez Grippe, Christine Klein, Norbert Brüggemann, Tobias Bäumer, Alexander Münchau, Anne Weissbach   +13 more
wiley   +1 more source

Physiological correlates of a simple saccadic-decision task to extended objects in superior colliculus

iScience
Summary: Saccadic eye movements direct gaze to objects of interest. Human studies show that saccade initiation latency depends on the size of the saccade target (the “size-latency effect”), perhaps reflecting a tradeoff between the cost of making a ...
Baptiste Caziot, Bonnie Cooper, Mark R. Harwood, Robert M. McPeek   +3 more
doaj   +1 more source

Saccade amplitude distribution.

, 2016
Kernel density estimates of Eyelink-detected saccade amplitude, averaged across conditions. The mode of this distribution falls within one degree of visual angle, a conventional criterium for the classification of microsaccades.
Jan Willem de Gee (3168912), Tomas Knapen (33341), Jan Brascamp (3168909), Stijn Nuiten (3168915), Sylco Hoppenbrouwers (3168906), Jan Theeuwes (22770)   +5 more
core   +1 more source

Saccade Adaptation in Williams-Beuren Syndrome

, 2006
PURPOSE. To investigate the capacity for rapid saccade adaptation in Williams-Beuren Syndrome (WBS), a genetic neurodevelopmental disorder, in which it has been observed that saccadic accuracy is severely reduced. METHODS.
Gerardina C Lagers-Van Haselen, Josef N Van Der Geest, van der Geest, Jos, Maarten A Frens, Frens, Maarten, van Haselen, GC   +5 more
core   +1 more source

Longitudinal Videofluorographic Dysphagia Measures in Progressive Supranuclear Palsy

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Dysphagia can lead to fatal aspiration pneumonia in progressive supranuclear palsy (PSP). Little is known about the longitudinal progression of dysphagia or whether it differs across PSP clinical variants. Objectives To characterize longitudinal changes in dysphagia across PSP variants and determine relationships with disease ...
Anna Chiara Cattani, Jerusha G. Bhaskaran, Farwa Ali, Julie Stierwalt, Federica Agosta, Massimo Filippi, Keith A. Josephs, Heather M. Clark, Jennifer L. Whitwell   +8 more
wiley   +1 more source

saccades.

https://aimc2024.pubpub.org/pub/vftqi55v/release ...
Charissa H. Tan, Heather E. Moss
  +5 more sources

Saccadic suppression [PDF]

Current Biology, 2010
openaire   +2 more sources

Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case‐Series and Literature Review

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Variants in AFG3‐Like Matrix AAA Peptidase, Subunit 2 (AFG3L2) gene are associated with diverse clinical phenotypes. Here, we describe phenotypic findings of two unrelated children with de novo heterozygous variant and one family with inherited heterozygous variant in AFG3L2 gene.
Sangeetha Yoganathan, Laura Tochen, Jacky Ganguly, Sayoni Roy Chowdhury, Haya S AlFaris, Vivek Pai, Andrea LeBlanc‐Millar, Sara Breitbart, Hrishikesh Kumar, Manohar Shroff, Arun Reginald, Grace Yoon, Alfonso Fasano, George M Ibrahim, Carolina Gorodetsky   +14 more
wiley   +1 more source