[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 …

[HTML][HTML] Machine‐learning in motor neuron diseases: Prospects and pitfalls

P Bede, KM Chang, EL Tan - European Journal of Neurology, 2022 - ncbi.nlm.nih.gov
Although machine-learning (ML) approaches have been extensively utilized in
neurodegenerative conditions, they can be challenging to implement in motor neuron …

[HTML][HTML] Thalamic, hippocampal and basal ganglia pathology in primary lateral sclerosis and amyotrophic lateral sclerosis: Evidence from quantitative imaging data

E Finegan, SLH Shing, RH Chipika, MC McKenna… - Data in brief, 2020 - Elsevier
Primary lateral sclerosis and amyotrophic lateral sclerosis are primarily associated with
motor cortex and corticospinal tract pathology. A standardised, prospective, single-centre …

Clinical profiles and patterns of neurodegeneration in amyotrophic lateral sclerosis: a cluster-based approach based on MR imaging metrics

G Milella, A Introna, DM Mezzapesa… - American Journal …, 2023 - Am Soc Neuroradiology
BACKGROUND AND PURPOSE: The previous studies described phenotype-associated
imaging findings in amyotrophic lateral sclerosis (ALS) with a prior categorization of patients …

[HTML][HTML] Evaluation and categorisation of individual patients based on white matter profiles: Single-patient diffusion data interpretation in neurodegeneration

M Tahedl, A Murad, J Lope, O Hardiman… - Journal of the neurological …, 2021 - Elsevier
The majority of radiology studies in neurodegenerative conditions infer group-level imaging
traits from group comparisons. While this strategy is helpful to define phenotype-specific …

[HTML][HTML] Mapping cortical disease-burden at individual-level in frontotemporal dementia: implications for clinical care and pharmacological trials

MC McKenna, M Tahedl, J Lope, RH Chipika… - Brain imaging and …, 2022 - Springer
Imaging studies of FTD typically present group-level statistics between large cohorts of
genetically, molecularly or clinically stratified patients. Group-level statistics are …

[HTML][HTML] Upper motor neuron disorders: primary lateral sclerosis, upper motor neuron dominant amyotrophic lateral sclerosis, and hereditary spastic paraplegia

T Fullam, J Statland - Brain Sciences, 2021 - mdpi.com
Following the exclusion of potentially reversible causes, the differential for those patients
presenting with a predominant upper motor neuron syndrome includes primary lateral …

[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 …

[HTML][HTML] Primary lateral sclerosis: an overview

V Vacchiano, L Bonan, R Liguori, G Rizzo - Journal of Clinical Medicine, 2024 - mdpi.com
Primary lateral sclerosis (PLS) is a rare neurodegenerative disorder which causes the
selective deterioration of the upper motor neurons (UMNs), sparing the lower motor neuron …

Neuroimaging in hereditary spastic paraplegias: from qualitative cues to precision biomarkers

G Mulkerrin, MC França Jr, J Lope… - Expert review of …, 2022 - Taylor & Francis
Introduction Hereditary spastic paraplegias (HSP) include a clinically and genetically
heterogeneous group of conditions. Novel imaging modalities have been increasingly …