Bildgebende Verfahren bei amyotropher Lateralsklerose und frontotemporaler Demenz

Translated title of the contribution: Imaging procedures for amyotrophic lateral sclerosis and frontotemporal dementia

T. Prell*, J. Grosskreutz

*Corresponding author for this work

Abstract

On the basis of recent genetic and neuropathological findings, amyotrophic lateral sclerosis and frontotemporal dementia can be regarded as 2 manifestations of a continuous disease. Novel imaging techniques showing comparable structural and functional changes in patient's white and grey matter support this view. Pathological changes in ALS clearly extend beyond the motor areas and disturbances in white matter, characterised by functional hypo- and hyperconnective areas, are a crucial factor in this disease. Vice versa FTD is not restricted to frontal atrophy, but shows involvement of motor areas and recruitment of compensatory brain regions. This review focus on the main results, obtained from conventional imaging and modern MRI techniques in ALS and FTD such as voxel-based morphometry, diffusion tensor imaging, magnetisation transfer imaging, MR spectroscopy, and functional MRI.

Translated title of the contributionImaging procedures for amyotrophic lateral sclerosis and frontotemporal dementia
Original languageGerman
JournalKlinische Neurophysiologie
Volume44
Issue number2
Pages (from-to)145-153
Number of pages9
ISSN1434-0275
DOIs
Publication statusPublished - 2013
Externally publishedYes

Research Areas and Centers

  • Centers: Center for Neuromuscular Diseases

Fingerprint

Dive into the research topics of 'Imaging procedures for amyotrophic lateral sclerosis and frontotemporal dementia'. Together they form a unique fingerprint.

Cite this