[HTML][HTML] Alterations in somatosensory, visual and auditory pathways in amyotrophic lateral sclerosis: an under-recognised facet of ALS

RH Chipika, G Mulkerrin, A Murad, J Lope… - Journal of integrative …, 2022 - imrpress.com
Background: While amyotrophic lateral sclerosis (ALS) is widely recognised as a multi-
network disorder with extensive frontotemporal and cerebellar involvement, sensory …

Amyotrophic lateral sclerosis: a clinical review

P Masrori, P Van Damme - European journal of neurology, 2020 - Wiley Online Library
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder affecting primarily the
motor system, but in which extra‐motor manifestations are increasingly recognized. The loss …

Primary lateral sclerosis

JM Statland, RJ Barohn, MM Dimachkie… - Neurologic …, 2015 - neurologic.theclinics.com
Primary lateral sclerosis (PLS) is a disorder of progressive upper motor neuron dysfunction,
in the absence of clinical signs of lower motor neuron involvement or family history …

[HTML][HTML] MRI data confirm the selective involvement of thalamic and amygdalar nuclei in amyotrophic lateral sclerosis and primary lateral sclerosis

RH Chipika, WF Siah, SLH Shing, E Finegan… - Data in brief, 2020 - Elsevier
A standardised imaging protocol was implemented to evaluate disease burden in specific
thalamic and amygdalar nuclei in 133 carefully phenotyped and genotyped motor neuron …

Neuroimaging in primary lateral sclerosis

EP Pioro, MR Turner, P Bede - Amyotrophic Lateral Sclerosis and …, 2020 - Taylor & Francis
Increased interest in the underlying pathogenesis of primary lateral sclerosis (PLS) and its
relationship to amyotrophic lateral sclerosis (ALS) has corresponded to a growing number of …

The stripe of primary lateral sclerosis: focal primary motor cortex hypometabolism seen on fluorodeoxyglucose F18 positron emission tomography

DO Claassen, KA Josephs, PJ Peller - Archives of neurology, 2010 - jamanetwork.com
Background Primary lateral sclerosis (PLS) is a progressive upper motor neuron
neurodegenerative condition. The diagnosis is made using clinical history, objective …

[HTML][HTML] Structural imaging differences and longitudinal changes in primary lateral sclerosis and amyotrophic lateral sclerosis

JY Kwan, A Meoded, LE Danielian, T Wu… - NeuroImage: Clinical, 2013 - Elsevier
Magnetic resonance imaging measures have been proposed as objective markers to study
upper motor neuron loss in motor neuron disorders. Cross-sectional studies have identified …

Motor neuron dysfunctions in the frontotemporal lobar degeneration spectrum: a clinical and neurophysiological study

C Cerami, A Marcone, C Crespi, S Iannaccone… - Journal of the …, 2015 - Elsevier
Background Although only a few frontotemporal lobar degeneration (FTLD) patients develop
frank amyotrophic lateral sclerosis (ALS), motor neuron dysfunctions (MNDys) occur in a …

Primary lateral sclerosis: clinical, radiological and molecular features

P Bede, PF Pradat, J Lope, P Vourc'h, H Blasco… - Revue …, 2022 - Elsevier
Abstract Primary Lateral Sclerosis (PLS) is an uncommon motor neuron disorder. Despite
the well-recognisable constellation of clinical manifestations, the initial diagnosis can be …

[HTML][HTML] Cross-sectional and longitudinal assessment of the upper cervical spinal cord in motor neuron disease

HK van der Burgh, HJ Westeneng, JM Meier… - NeuroImage: Clinical, 2019 - Elsevier
Background Amyotrophic lateral sclerosis (ALS) is a progressive neuromuscular disease
characterized by both upper and lower motor neuron degeneration. While neuroimaging …