Brain atrophy in primary lateral sclerosis

MC Tartaglia, V Laluz, A Rowe, K Findlater, DH Lee… - Neurology, 2009 - AAN Enterprises
Background: Primary lateral sclerosis (PLS) is an idiopathic upper motor neuron
degenerative disorder. The aim of this study was to compare brain volumes in patients with …

Whole-brain and regional brain atrophy in amyotrophic lateral sclerosis

DM Mezzapesa, A Ceccarelli… - American Journal …, 2007 - Am Soc Neuroradiology
BACKGROUND AND PURPOSE: Recent evidence from neuropsychologic and
neuroimaging studies suggests that central nervous system involvement in amyotrophic …

Decreased thickness of primary motor cortex in primary lateral sclerosis

JA Butman, MK Floeter - American journal of …, 2007 - Am Soc Neuroradiology
BACKGROUND AND PURPOSE: Primary lateral sclerosis (PLS) is a rare form of motor
neuron disease characterized by upper motor neuron dysfunction. Because pathologic …

Longitudinal course of cortical thickness decline in amyotrophic lateral sclerosis

C Schuster, E Kasper, J Machts, D Bittner… - Journal of …, 2014 - Springer
To determine longitudinal rates of cortical atrophy in classical Amyotrophic lateral sclerosis
(ALS) and ALS variants. Rates of cortical thinning were determined between 2 scans, 3–15 …

Loss of functional connectivity is an early imaging marker in primary lateral sclerosis

MG Clark, R Smallwood Shoukry… - … Lateral Sclerosis and …, 2018 - Taylor & Francis
Objective: The clinical diagnosis of primary lateral sclerosis can only be made after upper
motor neuron symptoms have progressed for several years without developing lower motor …

Continuum of frontal lobe impairment in amyotrophic lateral sclerosis

JM Murphy, RG Henry, S Langmore… - Archives of …, 2007 - jamanetwork.com
Objective To identify the nature and prevalence of cognitive and behavioral abnormalities in
patients with amyotrophic lateral sclerosis (ALS). Design Survey of clinical characteristics …

Structural MRI reveals cortical thinning in amyotrophic lateral sclerosis

E Verstraete, JH Veldink, J Hendrikse… - Journal of Neurology …, 2012 - jnnp.bmj.com
Objectives Amyotrophic lateral sclerosis (ALS) is a fatal disease characterised by combined
upper and lower motor neuron degeneration. An early and accurate diagnosis is important …

Widespread sensorimotor and frontal cortical atrophy in amyotrophic lateral sclerosis

J Grosskreutz, J Kaufmann, J Frädrich, R Dengler… - BMC neurology, 2006 - Springer
Background Widespread cortical atrophy in Amyotrophic Lateral Sclerosis (ALS) has been
described in neuropathological studies. The presence of cortical atrophy in conventional …

[HTML][HTML] Widespread subcortical grey matter degeneration in primary lateral sclerosis: a multimodal imaging study with genetic profiling

E Finegan, SLH Shing, RH Chipika, MA Doherty… - NeuroImage: Clinical, 2019 - Elsevier
Background Primary lateral sclerosis (PLS) is a low incidence motor neuron disease which
carries a markedly better prognosis than amyotrophic lateral sclerosis (ALS). Despite …

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 …