[HTML][HTML] Frontotemporal pathology in motor neuron disease phenotypes: insights from neuroimaging

MC McKenna, P Corcia, P Couratier, WF Siah… - Frontiers in …, 2021 - frontiersin.org
Frontotemporal involvement has been extensively investigated in amyotrophic lateral
sclerosis (ALS) but remains relatively poorly characterized in other motor neuron disease …

[HTML][HTML] Cerebellar pathology in motor neuron disease: neuroplasticity and neurodegeneration

RH Chipika, G Mulkerrin, PF Pradat… - Neural regeneration …, 2022 - journals.lww.com
Amyotrophic lateral sclerosis is a relentlessly progressive multi-system condition. The
clinical picture is dominated by upper and lower motor neuron degeneration, but extra-motor …

Phenotypic categorisation of individual subjects with motor neuron disease based on radiological disease burden patterns: A machine-learning approach

P Bede, A Murad, J Lope, SLH Shing, E Finegan… - Journal of the …, 2022 - Elsevier
Motor neuron disease is an umbrella term encompassing a multitude of clinically
heterogeneous phenotypes. The early and accurate categorisation of patients is hugely …

[HTML][HTML] Brainstem–cortex disconnection in amyotrophic lateral sclerosis: bulbar impairment, genotype associations, asymptomatic changes and biomarker …

M Tahedl, EL Tan, RH Chipika, JC Hengeveld… - Journal of …, 2023 - Springer
Background Bulbar dysfunction is a cardinal feature of ALS with important quality of life and
management implications. The objective of this study is the longitudinal evaluation of a large …

[HTML][HTML] Neurometabolic alterations in motor neuron disease: insights from magnetic resonance spectroscopy

F Christidi, E Karavasilis, GD Argyropoulos… - Journal of integrative …, 2022 - imrpress.com
Magnetic resonance spectroscopy (MRS) has contributed important academic insights in
motor neuron diseases (MNDs), particularly in amyotrophic lateral sclerosis (ALS). Over the …

[HTML][HTML] Propagation patterns in motor neuron diseases: Individual and phenotype-associated disease-burden trajectories across the UMN-LMN spectrum of MNDs

M Tahedl, SLH Shing, E Finegan, RH Chipika… - Neurobiology of …, 2022 - Elsevier
Motor neuron diseases encompass a divergent group of conditions with considerable
differences in clinical manifestations, survival, and genetic vulnerability. One of the key …

[HTML][HTML] Resting state fMRI analysis of pseudobulbar affect in Amyotrophic Lateral Sclerosis (ALS): motor dysfunction of emotional expression

F Trojsi, F Di Nardo, G D'Alvano, G Caiazzo… - Brain imaging and …, 2023 - Springer
Pseudobulbar affect (PBA), referring to exaggerated or inappropriate episodes of laughing
and/or crying without an apparent motivating stimulus, has been mainly attributed to bilateral …

[HTML][HTML] Infratentorial pathology in frontotemporal dementia: cerebellar grey and white matter alterations in FTD phenotypes

MC McKenna, RH Chipika, S Li Hi Shing, F Christidi… - Journal of …, 2021 - Springer
The contribution of cerebellar pathology to cognitive and behavioural manifestations is
increasingly recognised, but the cerebellar profiles of FTD phenotypes are relatively poorly …

Feature selection from magnetic resonance imaging data in ALS: a systematic review

TD Kocar, HP Müller, AC Ludolph… - … advances in chronic …, 2021 - journals.sagepub.com
Background: With the advances in neuroimaging in amyotrophic lateral sclerosis (ALS), it
has been speculated that multiparametric magnetic resonance imaging (MRI) is capable to …

[HTML][HTML] Radiological correlates of pseudobulbar affect: Corticobulbar and cerebellar components in primary lateral sclerosis

M Tahedl, EL Tan, WF Siah, JC Hengeveld… - Journal of the …, 2023 - Elsevier
Introduction Pseudobulbar affect (PBA) is a distressing symptom of a multitude of
neurological conditions affecting patients with a rage of neuroinflammatory, neurovascular …