[HTML][HTML] Patterns of grey and white matter changes differ between bulbar and limb onset amyotrophic lateral sclerosis

R Steinbach, T Prell, N Gaur, A Roediger, C Gaser… - NeuroImage: Clinical, 2021 - Elsevier
Abstract Amyotrophic Lateral Sclerosis (ALS) is a progressive neurodegenerative disease
that is characterized by a high heterogeneity in patients' disease course. Patients with bulbar …

Current and emerging ALS biomarkers: utility and potential in clinical trials

A Taga, NJ Maragakis - Expert review of neurotherapeutics, 2018 - Taylor & Francis
ABSTRACT Introduction: Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative
disorder which results in progressive muscle weakness as a prominent feature. However …

[HTML][HTML] Analysis of brain and spinal MRI measures in a common domain to investigate directional neurodegeneration in motor neuron disease

C Toh, A Keslake, T Payne, A Onwuegbuzie… - Journal of …, 2023 - Springer
Background Magnetic resonance imaging (MRI) of the brain and cervical spinal cord is often
performed in diagnostic evaluation of suspected motor neuron disease/amyotrophic lateral …

Regional alterations in cortical thickness and white matter integrity in amyotrophic lateral sclerosis

J Zhang, X Yin, L Zhao, AC Evans, L Song, B Xie… - Journal of …, 2014 - Springer
Previous neuroimaging studies have revealed that both gray matter (GM) and white matter
(WM) are altered in several morphological aspects in amyotrophic lateral sclerosis (ALS) …

[HTML][HTML] MRI cortical feature of bulbar impairment in patients with amyotrophic lateral sclerosis

G Donatelli, EC Ienco, M Costagli, G Migaleddu… - NeuroImage: Clinical, 2019 - Elsevier
The decline of voluntary bulbar functions such as speech and swallowing are among the
clinical manifestations of amyotrophic lateral sclerosis (ALS) influencing a worst prognosis …

Neural stem cells and human induced pluripotent stem cells to model rare CNS diseases

L De Filippis, C Zalfa, D Ferrari - CNS & Neurological …, 2017 - ingentaconnect.com
Background & Objective: Despite the great effort spent over recent decades to unravel the
pathological mechanisms underpinning the development of central nervous system …

[HTML][HTML] Relationship between clinical parameters and brain structure in sporadic amyotrophic lateral sclerosis patients according to onset type: a voxel-based …

HJ Kim, M de Leon, X Wang, HY Kim, YJ Lee, YH Kim… - PloS one, 2017 - journals.plos.org
Background and purpose Amyotrophic lateral sclerosis (ALS) is a rapidly progressing,
phenotypically heterogeneous neurodegenerative disease affecting mainly the motor …

[HTML][HTML] Neuroimaging as a new diagnostic modality in amyotrophic lateral sclerosis

E Verstraete, BR Foerster - Neurotherapeutics, 2015 - Elsevier
Amyotrophic lateral sclerosis (ALS) is characterized by progressive degeneration of upper
and lower motor neurons, with variable involvement of extramotor brain regions. Currently …

[HTML][HTML] Motor cortical patterns of upper motor neuron pathology in amyotrophic lateral sclerosis: A 3 T MRI study with iron-sensitive sequences

G Donatelli, M Costagli, P Cecchi, G Migaleddu… - NeuroImage: Clinical, 2022 - Elsevier
Background Patterns of initiation and propagation of disease in Amyotrophic Lateral
Sclerosis (ALS) are still partly unknown. Single or multiple foci of neurodegeneration …

Side of limb‐onset predicts laterality of gray matter loss in amyotrophic lateral sclerosis

Q Zhang, C Mao, J Jin, C Niu, L Bai… - BioMed Research …, 2014 - Wiley Online Library
Conflicting findings have been reported regarding the lateralized brain abnormality in
patients with amyotrophic lateral sclerosis (ALS). In this study, we aimed to investigate the …