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 …
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 …
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 …
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 …
(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 …
motor neuron symptoms have progressed for several years without developing lower motor …
Continuum of frontal lobe impairment in amyotrophic lateral sclerosis
Objective To identify the nature and prevalence of cognitive and behavioral abnormalities in
patients with amyotrophic lateral sclerosis (ALS). Design Survey of clinical characteristics …
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 …
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 …
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
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 …
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 …