Unbiased MRI analyses identify micropathologic differences between upper motor neuron-predominant ALS phenotypes

V Rajagopalan, EP Pioro - Frontiers in Neuroscience, 2019 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) is an incurable and progressively fatal
neurodegenerative disease that manifests with distinct clinical phenotypes, which are seen …

[HTML][HTML] Altered white matter microarchitecture in amyotrophic lateral sclerosis: a voxel-based meta-analysis of diffusion tensor imaging

F Zhang, G Chen, M He, J Dai, H Shang, Q Gong… - NeuroImage: Clinical, 2018 - Elsevier
Background The results of recent diffusion tensor imaging (DTI) studies on amyotrophic
lateral sclerosis (ALS) are inconclusive and controversial. We performed a voxel-based …

Clinical spectrum of amyotrophic lateral sclerosis (ALS)

LI Grad, GA Rouleau, J Ravits… - Cold Spring …, 2017 - perspectivesinmedicine.cshlp.org
Amyotrophic lateral sclerosis (ALS) is primarily characterized by progressive loss of motor
neurons, although there is marked phenotypic heterogeneity between cases. Typical, or …

[HTML][HTML] Structural MRI outcomes and predictors of disease progression in amyotrophic lateral sclerosis

EG Spinelli, N Riva, PMV Rancoita, P Schito… - NeuroImage: Clinical, 2020 - Elsevier
Background and aims Considering the great heterogeneity of amyotrophic lateral sclerosis
(ALS), the identification of accurate prognostic predictors is fundamental for both the clinical …

Neurochemical correlates of functional decline in amyotrophic lateral sclerosis

I Cheong, DK Deelchand, LE Eberly… - Journal of Neurology …, 2019 - jnnp.bmj.com
Objective To determine whether proton magnetic resonance spectroscopy (1H-MRS) can
detect neurochemical changes in amyotrophic lateral sclerosis (ALS) associated with …

The value of magnetic resonance imaging as a biomarker for amyotrophic lateral sclerosis: a systematic review

G Grolez, C Moreau, V Danel-Brunaud, C Delmaire… - BMC neurology, 2016 - Springer
Background Amyotrophic lateral sclerosis (ALS) is a fatal, rapidly progressive
neurodegenerative disease that mainly affects the motor system. A number of potentially …

[HTML][HTML] Longitudinal evaluation of cerebral and spinal cord damage in amyotrophic lateral sclerosis

M de Albuquerque, LMT Branco, TJR Rezende… - Neuroimage: Clinical, 2017 - Elsevier
Objective To evaluate MRI-based parameters as biomarkers of Amyotrophic Lateral
Sclerosis (ALS) progression. Methods Twenty-seven patients and 27 controls performed two …

Widespread sensorimotor and frontal cortical atrophy in amyotrophic lateral sclerosis

J Grosskreutz, J Kaufmann, J Frädrich, R Dengler… - BMC neurology, 2006 - Springer
Background Widespread cortical atrophy in Amyotrophic Lateral Sclerosis (ALS) has been
described in neuropathological studies. The presence of cortical atrophy in conventional …

Resting state functional MRI brain signatures of fast disease progression in amyotrophic lateral sclerosis: a retrospective study

F Trojsi, F Di Nardo, M Siciliano, G Caiazzo… - … Lateral Sclerosis and …, 2021 - Taylor & Francis
Objective Advanced neuroimaging techniques may offer the potential to monitor disease
spreading in amyotrophic lateral sclerosis (ALS). We aim to investigate brain functional and …

Implications of structural and functional brain changes in amyotrophic lateral sclerosis

T Dharmadasa, W Huynh, J Tsugawa… - Expert Review of …, 2018 - Taylor & Francis
Introduction: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that causes
progressive muscle weakness and disability, eventually leading to death. Heterogeneity of …