Results 111 to 120 of about 25,095 (260)
White matter hyperintensities (WMH) are very widespread in older adults and are imaging features of both cerebral small‐vessel disease and white matter microstructural impairments. Recent studies have demonstrated a close association between WMH and some
Hui Huang +7 more
doaj +1 more source
Background The aim of this study was to investigate the associations between pulse pressure (PP) and age‐related structural brain changes including brain volumes, white matter hyperintensities (WMH), fractional anisotropy, silent brain lesions ...
Marina Cecelja +3 more
doaj +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
Abstract Background Childhood‐onset hyperkinetic movement disorders occur in a range of genetic conditions. Recently, there has been an increase in recognition of hyperkinetic movement disorders, mainly dystonia, chorea and dyskinesia, with monogenic conditions associated with neurodevelopmental delay (NDD) and also with developmental and epileptic ...
Hugo Morales‐Briceño +6 more
wiley +1 more source
The Robustness of White Matter Brain Networks Decreases with Aging
Background: White matter (WM) is a principal component of the human brain, forming the structural basis for neural transmission between cortico-cortical and subcortical structures.
Chenye Huang, Xie Wang, Daojun Xie
doaj +1 more source
A Multiple Sclerosis MRI Dataset with Tri-Mask Annotations for Lesion Segmentation
Multiple sclerosis (MS) lesion segmentation from MRI is essential for diagnosis, monitoring, and treatment evaluation, yet existing datasets exhibit limited geographic diversity, scanner vendor bias, and inability to distinguish normal from pathological ...
Mahdi Bashiri Bawil +4 more
doaj +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
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
Characterization of white matter hyperintensities in Down syndrome
AbstractINTRODUCTIONIn Down syndrome (DS), white matter hyperintensities (WMHs) are highly prevalent, yet their topography and association with sociodemographic data and Alzheimer's disease (AD) biomarkers remain largely unexplored.METHODSIn 261 DS adults and 131 euploid controls, fluid‐attenuated inversion recovery magnetic resonance imaging scans ...
Morcillo‐Nieto, Alejandra O. +26 more
openaire +4 more sources
Abstract Background Perinatal hypoxic–ischemic encephalopathy (HIE) is a severe condition resulting from impaired oxygen delivery to the developing brain, often leading to both motor deficits and dystonia‐dyskinetic syndromes (DDS). In selected cases, deep brain stimulation of the globus pallidus internus (GPi‐DBS) may provide a therapeutic option ...
Marylou Grasso +7 more
wiley +1 more source

