Structural and diffusion imaging versus clinical assessment to monitor amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis is a progressive neurodegenerative disease that affects upper and lower motor neurons. Observational and intervention studies can be tracked using clinical measures such as the revised Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS-R) but for a complete u...
Main Authors: | Arturo Cardenas-Blanco, Judith Machts, Julio Acosta-Cabronero, Joern Kaufmann, Susanne Abdulla, Katja Kollewe, Susanne Petri, Stefanie Schreiber, Hans-Jochen Heinze, Reinhard Dengler, Stefan Vielhaber, Peter J. Nestor |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2016-01-01
|
Series: | NeuroImage: Clinical |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2213158216300523 |
Similar Items
-
Assessment of therapeutic response of edaravone and riluzole combination therapy in amyotrophic lateral sclerosis patients
by: Swapnil Samadhiya, et al.
Published: (2022-01-01) -
The Dyspnea-ALS-Scale (DALS-15) optimizes individual treatment in patients with amyotrophic lateral sclerosis (ALS) suffering from dyspnea
by: Susanne Vogt, et al.
Published: (2019-06-01) -
ALSFRS-R-SE: an adapted, annotated, and self-explanatory version of the revised amyotrophic lateral sclerosis functional rating scale
by: André Maier, et al.
Published: (2022-12-01) -
Clinical characteristics of patients with Amyotrophic Lateral Sclerosis in the Republic of Srpska
by: Lepir Igor, et al.
Published: (2019-01-01) -
Working memory in ALS patients: preserved performance but marked changes in underlying neuronal networks.
by: Tino Zaehle, et al.
Published: (2013-01-01)