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 …

[HTML][HTML] Brain metabolic differences between pure bulbar and pure spinal ALS: a 2-[18F]FDG-PET study

A Canosa, A Martino, A Giuliani, C Moglia, R Vasta… - Journal of …, 2023 - Springer
Background MRI studies reported that ALS patients with bulbar and spinal onset showed
focal cortical changes in corresponding regions of the motor homunculus. We evaluated the …

Clinical profiles and patterns of neurodegeneration in amyotrophic lateral sclerosis: a cluster-based approach based on MR imaging metrics

G Milella, A Introna, DM Mezzapesa… - American Journal …, 2023 - Am Soc Neuroradiology
BACKGROUND AND PURPOSE: The previous studies described phenotype-associated
imaging findings in amyotrophic lateral sclerosis (ALS) with a prior categorization of patients …

The concept and diagnostic criteria of primary lateral sclerosis

V Wais, A Rosenbohm, S Petri… - Acta Neurologica …, 2017 - Wiley Online Library
Objectives Primary lateral sclerosis (PLS) is commonly considered as a motor neuron
disease (MND) variant which almost exclusively affects upper motor neurons (UMN). There …

[HTML][HTML] Extent of cortical involvement in amyotrophic lateral sclerosis–an analysis based on cortical thickness

J Thorns, H Jansma, T Peschel, J Grosskreutz… - BMC neurology, 2013 - Springer
Background Besides the defining involvement of upper and lower motor neurons, the
involvement of extramotor structures has been increasingly acknowledged in amyotrophic …

[HTML][HTML] Applying the D50 disease progression model to gray and white matter pathology in amyotrophic lateral sclerosis

R Steinbach, M Batyrbekova, N Gaur, A Voss… - NeuroImage: Clinical, 2020 - Elsevier
Therapeutic management and research in Amyotrophic Laterals Sclerosis (ALS) have been
limited by the substantial heterogeneity in progression and anatomical spread that are …

[HTML][HTML] Primary lateral sclerosis: an overview

V Vacchiano, L Bonan, R Liguori, G Rizzo - Journal of Clinical Medicine, 2024 - mdpi.com
Primary lateral sclerosis (PLS) is a rare neurodegenerative disorder which causes the
selective deterioration of the upper motor neurons (UMNs), sparing the lower motor neuron …

Brain MR imaging in patients with lower motor neuron–predominant disease

EG Spinelli, F Agosta, PM Ferraro, N Riva, C Lunetta… - Radiology, 2016 - pubs.rsna.org
Purpose To investigate the patterns of cortical thinning and white matter tract damage in
patients with lower motor neuron (LMN)–predominant disease compared with healthy …

[HTML][HTML] Combinatory biomarker use of cortical thickness, MUNIX, and ALSFRS-R at baseline and in longitudinal courses of individual patients with amyotrophic lateral …

AM Wirth, A Khomenko, D Baldaranov, I Kobor… - Frontiers in …, 2018 - frontiersin.org
Objective: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative process
affecting upper and lower motor neurons as well as non-motor systems. In this study …

[HTML][HTML] Cortical structure and the risk of amyotrophic lateral sclerosis: a bidirectional Mendelian randomization study

H Jia, Z Li, F Guo, Z Hua, X Zhou, X Li, R Li… - Progress in Neuro …, 2024 - Elsevier
Background Current observational studies indicate progressive brain atrophy is closely
associated with the clinical feature of amyotrophic lateral sclerosis. However, it is unclear …