Hyperintensity of the corticospinal tract on FLAIR: A simple and sensitive objective upper motor neuron degeneration marker in clinically verified amyotrophic lateral …

J Jin, F Hu, Q Zhang, R Jia, J Dang - Journal of the neurological sciences, 2016 - Elsevier
Objective The involvement of upper motor neuron (UMN) degeneration is crucial to the
diagnosis of amyotrophic lateral sclerosis (ALS). However, it is difficult to detect in the early …

Magnetic resonance imaging in amyotrophic lateral sclerosis

K Kollewe, S Körner, R Dengler, S Petri… - Neurology research …, 2012 - Wiley Online Library
Amyotrophic lateral sclerosis (ALS) is a rapidly progressing neurodegenerative disorder
which is incurable to date. As there are many ongoing studies with therapeutic candidates, it …

[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 …

Not a benign motor neuron disease: longitudinal imaging captures relentless motor connectome disintegration in primary lateral sclerosis

M Tahedl, EL Tan, SLH Shing… - European Journal of …, 2023 - Wiley Online Library
Background and purpose Primary lateral sclerosis (PLS) is a progressive upper motor
neuron disorder associated with considerable clinical disability. Symptoms are typically …

Advanced neuroimaging approaches in amyotrophic lateral sclerosis: refining the clinical diagnosis

J Kassubek, HP Müller - Expert review of neurotherapeutics, 2020 - Taylor & Francis
Introduction: In the last decade, multiparametric magnetic resonance imaging (MRI) has
achieved tremendous advances in applications to amyotrophic lateral sclerosis (ALS) to …

Widespread grey matter pathology dominates the longitudinal cerebral MRI and clinical landscape of amyotrophic lateral sclerosis

RAL Menke, S Körner, N Filippini, G Douaud, S Knight… - Brain, 2014 - academic.oup.com
Diagnosis, stratification and monitoring of disease progression in amyotrophic lateral
sclerosis currently rely on clinical history and examination. The phenotypic heterogeneity of …

[HTML][HTML] Evolving diagnostic criteria in primary lateral sclerosis: the clinical and radiological basis of “probable PLS”

E Finegan, SLH Shing, WF Siah, RH Chipika… - Journal of the …, 2020 - Elsevier
Introduction Primary lateral sclerosis is a rare neurodegenerative disorder of the upper
motor neurons. Diagnostic criteria have changed considerably over the years, and the …

[HTML][HTML] Spinal cord imaging in amyotrophic lateral sclerosis: historical concepts—novel techniques

MM El Mendili, G Querin, P Bede, PF Pradat - Frontiers in neurology, 2019 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) is the most common adult onset motor neuron disease
with no effective disease modifying therapies at present. Spinal cord degeneration is a …

Structural MRI correlates of amyotrophic lateral sclerosis progression

J Senda, N Atsuta, H Watanabe… - Journal of Neurology …, 2017 - jnnp.bmj.com
Purpose Amyotrophic lateral sclerosis (ALS) presents with varying degrees of brain
degeneration that can extend beyond the corticospinal tract (CST). Furthermore, the clinical …

[HTML][HTML] Positron emission tomography molecular imaging biomarkers for amyotrophic lateral sclerosis

S Chew, N Atassi - Frontiers in neurology, 2019 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder with limited
treatment options. Despite decades of therapeutic development, only two modestly …