[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 …

[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 …

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 …

Not a benign motor neuron disease: longitudinal imaging captures relentless motor connectome disintegration in primary lateral sclerosis

M Tahedl, EL Tan, SLH Shing… - European Journal of …, 2023 - Wiley Online Library
Background and purpose Primary lateral sclerosis (PLS) is a progressive upper motor
neuron disorder associated with considerable clinical disability. Symptoms are typically …

[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] Alterations in somatosensory, visual and auditory pathways in amyotrophic lateral sclerosis: an under-recognised facet of ALS

RH Chipika, G Mulkerrin, A Murad, J Lope… - Journal of integrative …, 2022 - imrpress.com
Background: While amyotrophic lateral sclerosis (ALS) is widely recognised as a multi-
network disorder with extensive frontotemporal and cerebellar involvement, sensory …

[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 …

[HTML][HTML] Primary Lateral Sclerosis: Clinical, radiological and molecular features

P Bede, PF Pradat, J Lope, P Vourc'h, H Blasco… - Revue …, 2022 - Elsevier
Abstract Primary Lateral Sclerosis (PLS) is an uncommon motor neuron disorder. Despite
the well-recognisable constellation of clinical manifestations, the initial diagnosis can be …

Promises and pitfalls of imaging-based biomarkers in motor neuron diseases

EL Tan, P Bede, PF Pradat - Current Opinion in Neurology, 2023 - journals.lww.com
Although we acknowledge the academic achievements of large descriptive studies, an
unmet priority of neuroimaging in MND is the development of robust diagnostic, prognostic …