In vivo evidence for cell body loss in cortical lesions in people with multiple sclerosis

Cortical cell body loss in multiple sclerosis is most pronounced in cortical lesions and also present in normal-appearing cortex. Gradients of diffusion microstructural alterations moving outward from cortical lesions toward normal-appearing cortex highlight the potential of high-gradient diffusion MRI to identify both focal and diffuse cortical pathology.

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Publication Details

Journal
Annals of Clinical and Translational Neurology
Published
2024-12-13
DOI
https://doi.org/10.1002/acn3.52237
Citations
5
Primary Topic
Multiple Sclerosis Research Studies
Type
article
Field-Weighted Citation Impact
2.12

Funders

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article

In vivo evidence for cell body loss in cortical lesions in people with multiple sclerosis

Samantha Noteboom, Florence L. Chiang, Eric C. Klawiter, Martijn D. Steenwijk et al.
5 citations
Annals of Clinical and Translational Neurology
Multiple Sclerosis Research Studies
2.12
article

In vivo evidence for cell body loss in cortical lesions in people with multiple sclerosis

Samantha Noteboom, Florence L. Chiang, Eric C. Klawiter, Martijn D. Steenwijk, Menno Michiel Schoonheim, Eva A. Krijnen, Susie Y. Huang, Hansol Lee
article en
5 citations

Abstract

Cortical cell body loss in multiple sclerosis is most pronounced in cortical lesions and also present in normal-appearing cortex. Gradients of diffusion microstructural alterations moving outward from cortical lesions toward normal-appearing cortex highlight the potential of high-gradient diffusion MRI to identify both focal and diffuse cortical pathology.

Annals of Clinical and Translational NeurologyVol. 12(1)
Harvard University (US), Massachusetts General Hospital (US), Amsterdam Neuroscience (NL), Athinoula A. Martinos Center for Biomedical Imaging (US), Amsterdam University Medical Centers (NL), Vrije Universiteit Amsterdam (NL)
Koning Boudewijnstichting, National Institutes of Health
Good health and well-being
Openalex Percentile: Top 12%
Multiple Sclerosis Research Studies
2.12
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