Results 151 to 160 of about 24,272 (299)
Movement Disorders in Developmental and Epileptic Encephalopathies
Abstract Background Monogenic developmental and epileptic encephalopathies (DEE) frequently feature co‐occurring movement disorders. Gene discovery has expanded epilepsy‐dyskinesia syndromes (EDS) from classic associations such as stereotypies in Rett syndrome to PRRT2‐related infantile seizures with paroxysmal dyskinesia and crouched gait in SCN1A ...
Shekeeb Mohammad +2 more
wiley +1 more source
Migraine and MRI: uncovering potential associations
Objective This study aims to investigate the association between patients with migraine headaches and brain magnetic resonance imaging (MRI) findings.
Khalid Abdalla +3 more
doaj +1 more source
Pattern and significance of white matter abnormalities in myotonic dystrophy type 1: an MRI study.
We reviewed the brain MRI of 66 patients with the adult form of myotonic dystrophy type 1 (DM1) to evaluate the extent and significance of white matter involvement and to look for a pattern of MRI abnormalities suggestive of DM1.
V. Bonavita +6 more
core +1 more source
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 +14 more
wiley +1 more source
Physical activity and white matter hyperintensity one year after stroke: An exploratory analysis from the Cognition And Neocortical Volume After Stroke (CANVAS ...
B Campbell (11487520) +6 more
core
Unadjusted and adjusted models of the association between standardized whole brain white matter hyperintensity volume (WMHV/TCV) and functional status, stratified by mobility versus non-mobility domains.
Ying-Kuen Cheung (4686259) +6 more
core +1 more source
Abstract Background Primary brain calcification (PBC) is a genetic disease featuring movement disorders, cognitive impairment, and/or psychiatric symptoms. Computed tomography (CT) scan identifies brain calcification but poorly correlates with patients' clinical phenotype; the role of magnetic resonance imaging (MRI) is yet undefined.
Giovanni Librizzi +9 more
wiley +1 more source
In patient B at nine months of age, thin corpus callosum (A), T2 diffuse hyperintensity in the peri-Rolandic white matter (B) and posterior occipital white matter region (C) were seen; FLAIR diffuse hyperintensity in the white matter region was also seen
Magalie Leduc (2633278) +28 more
core +1 more source
Abstract Background Blood–brain barrier disruption is increasingly recognized in synucleinopathies, but the role of the endothelial glycocalyx (GLX) in Parkinson's disease (PD) and multiple system atrophy (MSA) remains unclear. Objectives The aim was to determine whether plasma GLX markers differ between PD, MSA, and healthy controls (HC), relate to ...
Jonas Folke +15 more
wiley +1 more source
Unadjusted and adjusted models of the association between standardized whole brain white matter hyperintensity volume (WMHV/TCV*100) and functional status.
Ying-Kuen Cheung (4686259) +6 more
core +1 more source

