[HTML][HTML] Segmental alterations of the corpus callosum in motor neuron disease: A DTI and texture analysis in 575 patients

M Münch, HP Müller, A Behler, AC Ludolph… - NeuroImage: Clinical, 2022 - Elsevier
Introduction Within the core neuroimaging signature of amyotrophic lateral sclerosis (ALS),
the corpus callosum (CC) is increasingly recognized as a consistent feature. The aim of this …

High-resolution 7T MR imaging of the motor cortex in amyotrophic lateral sclerosis

M Cosottini, G Donatelli, M Costagli… - American journal …, 2016 - Am Soc Neuroradiology
BACKGROUND AND PURPOSE: Amyotrophic lateral sclerosis is a progressive motor
neuron disorder that involves degeneration of both upper and lower motor neurons. In …

Cerebral atrophy in amyotrophic lateral sclerosis parallels the pathological distribution of TDP43

M Dadar, AL Manera, L Zinman, L Korngut… - Brain …, 2020 - academic.oup.com
Amyotrophic lateral sclerosis is a neurodegenerative disease characterized by a preferential
involvement of both upper and lower motor neurons. Evidence from neuroimaging and post …

[HTML][HTML] Ultra high-field (7tesla) magnetic resonance spectroscopy in Amyotrophic Lateral Sclerosis

N Atassi, M Xu, C Triantafyllou, B Keil, R Lawson… - PLoS …, 2017 - journals.plos.org
The main objective of this study was to utilize high field (7T) in vivo proton magnetic
resonance imaging to increase the ability to detect metabolite changes in people with ALS …

A systematic and comprehensive review on disease-causing genes in amyotrophic lateral sclerosis

E Srinivasan, R Rajasekaran - Journal of Molecular Neuroscience, 2020 - Springer
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder and is characterized by
degeneration and axon loss from the upper motor neuron, that descends from the lower …

[HTML][HTML] 1H Magnetic Resonance Spectroscopy to Understand the Biological Basis of ALS, Diagnose Patients Earlier, and Monitor Disease Progression

S Caldwell, DL Rothman - Frontiers in Neurology, 2021 - frontiersin.org
At present, limited biomarkers exist to reliably understand, diagnose, and monitor the
progression of amyotrophic lateral sclerosis (ALS), a fatal neurological disease …

Mitochondrial protein import dysfunction in pathogenesis of neurodegenerative diseases

S Goyal, RK Chaturvedi - Molecular Neurobiology, 2021 - Springer
Mitochondria play an essential role in maintaining energy homeostasis and cellular survival.
In the brain, higher ATP production is required by mature neurons for communication. Most …

[HTML][HTML] Imaging neurochemistry and brain structure tracks clinical decline and mechanisms of ALS in patients

OC Andronesi, K Nicholson, K Jafari-Khouzani… - Frontiers in …, 2020 - frontiersin.org
Background: Oxidative stress and protein aggregation are key mechanisms in amyotrophic
lateral sclerosis (ALS) disease. Reduced glutathione (GSH) is the most important …

Longitudinal course of cortical thickness decline in amyotrophic lateral sclerosis

C Schuster, E Kasper, J Machts, D Bittner… - Journal of …, 2014 - Springer
To determine longitudinal rates of cortical atrophy in classical Amyotrophic lateral sclerosis
(ALS) and ALS variants. Rates of cortical thinning were determined between 2 scans, 3–15 …

Multi-modal signatures of tau pathology, neuronal fiber integrity, and functional connectivity in traumatic brain injury

DW Wooten, L Ortiz-Terán, N Zubcevik… - Journal of …, 2019 - liebertpub.com
Abstract [18F] AV-1451 (aka 18F-Flortaucipir,[18F] T807) was developed for positron-
emission tomography (PET) imaging of paired helical filaments of hyperphosphorylated tau …