Extra-motor cerebral changes and manifestations in primary lateral sclerosis
E Finegan, SLH Shing, RH Chipika, KM Chang… - Brain imaging and …, 2021 - Springer
Primary lateral sclerosis (PLS) is classically considered a 'pure'upper motor neuron disorder.
Motor cortex atrophy and pyramidal tract degeneration are thought to be pathognomonic of …
Motor cortex atrophy and pyramidal tract degeneration are thought to be pathognomonic of …
The clinical and radiological profile of primary lateral sclerosis: a population-based study
Background Primary lateral sclerosis is a progressive upper-motor-neuron disorder
associated with markedly longer survival than ALS. In contrast to ALS, the genetic …
associated with markedly longer survival than ALS. In contrast to ALS, the genetic …
[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 …
motor neurons. Diagnostic criteria have changed considerably over the years, and the …
[HTML][HTML] Supra-and infra-tentorial degeneration patterns in primary lateral sclerosis: a multimodal longitudinal neuroradiology study
J Kleinerova, M Tahedl, EL Tan, S Delaney… - Journal of …, 2024 - Springer
Background Primary lateral sclerosis (PLS) is traditionally solely associated with progressive
upper motor neuron dysfunction manifesting in limb spasticity, gait impairment, bulbar …
upper motor neuron dysfunction manifesting in limb spasticity, gait impairment, bulbar …
[HTML][HTML] Widespread subcortical grey matter degeneration in primary lateral sclerosis: a multimodal imaging study with genetic profiling
Background Primary lateral sclerosis (PLS) is a low incidence motor neuron disease which
carries a markedly better prognosis than amyotrophic lateral sclerosis (ALS). Despite …
carries a markedly better prognosis than amyotrophic lateral sclerosis (ALS). Despite …
[HTML][HTML] Extramotor damage is associated with cognition in primary lateral sclerosis patients
Objectives This is a cross-sectional study aimed at investigating cognitive performances in
patients with primary lateral sclerosis (PLS) and using diffusion tensor (DT) magnetic …
patients with primary lateral sclerosis (PLS) and using diffusion tensor (DT) magnetic …
A case series of PLS patients with frontotemporal dementia and overview of the literature
BS de Vries, LMM Rustemeijer… - … Lateral Sclerosis and …, 2017 - Taylor & Francis
Objective: Primary lateral sclerosis (PLS) is a rare form of motor neuron disease
characterised by UMN degeneration leading to slowly progressive spasticity. Whether it is a …
characterised by UMN degeneration leading to slowly progressive spasticity. Whether it is a …
Clinicopathological features of primary lateral sclerosis are different from amyotrophic lateral sclerosis
AJ Hudson, JA Kiernan, DG Munoz, CE Pringle… - Brain research …, 1993 - Elsevier
Primary lateral sclerosis (PLS) bears close resemblance to cases of amyotrophic lateral
sclerosis (ALS) presenting with spasticity, but histopathological studies have shown …
sclerosis (ALS) presenting with spasticity, but histopathological studies have shown …
Primary lateral sclerosis: consensus diagnostic criteria
Primary lateral sclerosis (PLS) is a neurodegenerative disorder of the adult motor system.
Characterised by a slowly progressive upper motor neuron syndrome, the diagnosis is …
Characterised by a slowly progressive upper motor neuron syndrome, the diagnosis is …
Primary lateral sclerosis: further clarification
N Le Forestier, T Maisonobe, L Spelle, A Lesort… - Journal of the …, 2001 - Elsevier
Primary lateral sclerosis (PLS) has been defined as a rare. Non-hereditary disease
characterized by progressive spinobulbar spasticity, related to the exclusive involvement of …
characterized by progressive spinobulbar spasticity, related to the exclusive involvement of …