Assessment of white matter tract damage in patients with amyotrophic lateral sclerosis: a diffusion tensor MR imaging tractography study

F Agosta, E Pagani, M Petrolini… - American Journal …, 2010 - Am Soc Neuroradiology
BACKGROUND AND PURPOSE: Most DTI studies in ALS have been limited to the
assessment of the CST damage. In this study, we used DTI tractography to investigate …

Radial diffusivity as an imaging biomarker for early diagnosis of non-demented amyotrophic lateral sclerosis

Y Bao, L Yang, Y Chen, B Zhang, H Li, W Tang… - European …, 2018 - Springer
Objectives To explore the sensitivity of potential DTI-based biomarkers in detecting
microstructural changes for whole-brain white matter in early stage amyotrophic lateral …

[HTML][HTML] Tract-specific analysis improves sensitivity of spinal cord diffusion MRI to cross-sectional and longitudinal changes in amyotrophic lateral sclerosis

PK Pisharady, LE Eberly, I Cheong… - Communications …, 2020 - nature.com
Amyotrophic lateral sclerosis (ALS) is a late-onset fatal neurodegenerative disease that
causes progressive degeneration of motor neurons in the brain and the spinal cord …

[HTML][HTML] Temporal and spatial progression of microstructural cerebral degeneration in ALS: A multicentre longitudinal diffusion tensor imaging study

HP Müller, A Abrahao, C Beaulieu, M Benatar… - NeuroImage: Clinical, 2024 - Elsevier
Objective The corticospinal tract (CST) reveals progressive microstructural alterations in ALS
measurable by DTI. The aim of this study was to evaluate fractional anisotropy (FA) along …

A meta-analysis of diffusion tensor imaging studies in amyotrophic lateral sclerosis

JP Li, PL Pan, W Song, R Huang, K Chen… - Neurobiology of …, 2012 - Elsevier
Studies involving diffusion tensor imaging (DTI) of amyotrophic lateral sclerosis (ALS) with
whole-brain voxel-based analysis yielded variable findings. A systematic review was …

Diffusion tensor MRI as a diagnostic tool of upper motor neuron involvement in amyotrophic lateral sclerosis

YH Hong, KW Lee, JJ Sung, KH Chang… - Journal of the neurological …, 2004 - Elsevier
BACKGROUND: Clinical identification of upper motor neuron (UMN) dysfunction in
amyotrophic lateral sclerosis (ALS) is often difficult, particularly early in the course of the …

Quantitative diffusion tensor imaging in amyotrophic lateral sclerosis

CA Sage, RR Peeters, A Görner, W Robberecht… - Neuroimage, 2007 - Elsevier
OBJECTIVE: Aim of present study was to evaluate changes in diffusion tensor imaging (DTI)
parameters in the whole brain of 28 patients with amyotrophic lateral sclerosis (ALS) …

[HTML][HTML] 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 …

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] Microstructural changes across different clinical milestones of disease in amyotrophic lateral sclerosis

F Trojsi, G Caiazzo, D Corbo, G Piccirillo, V Cristillo… - PloS one, 2015 - journals.plos.org
Neurodegenerative process in amyotrophic lateral sclerosis (ALS) has been proven to
involve several cortical and subcortical brain regions within and beyond motor areas …