Objective To evaluate multimodal MRI of the spinal cord in predicting disease progression
and one-year clinical status in amyotrophic lateral sclerosis (ALS) patients. Materials and …

Objective To evaluate MRI-based parameters as biomarkers of Amyotrophic Lateral
Sclerosis (ALS) progression. Methods Twenty-seven patients and 27 controls performed two …

Background and purpose Assessing survival is a critical issue in patients with amyotrophic
lateral sclerosis (ALS). Neuroimaging seems to be promising in the assessment of disease …

Our objective was to investigate spinal cord (SC) atrophy in amyotrophic lateral sclerosis
(ALS) patients, and to determine whether it correlates with clinical parameters. Forty-three …

In this preliminary study, our objective was to investigate the potential of high‐resolution
anatomical imaging, diffusion tensor imaging (DTI) and conventional/inhomogeneous …

Amyotrophic lateral sclerosis is a progressive neurodegenerative disease that affects upper
and lower motor neurons. Observational and intervention studies can be tracked using …

Purpose Amyotrophic lateral sclerosis (ALS) presents with varying degrees of brain
degeneration that can extend beyond the corticospinal tract (CST). Furthermore, the clinical …

We investigated whether conventional and diffusion tensor (DT) magnetic resonance
imaging (MRI) features of the corticospinal tract (CST) contribute to the prediction of the long …

Whether longitudinal diffusion tensor MRI imaging (DTI) can capture disease progression in
patients with amyotrophic lateral sclerosis (ALS) is unclear. The primary goal of this study …

Motor neuron damage and cortical spinal tract (CST) degeneration are pathological features
of amyotrophic lateral sclerosis (ALS). We combined whole-brain diffusion tensor imaging …