[HTML][HTML] Increased cerebral integrity metrics in poliomyelitis survivors: putative adaptation to longstanding lower motor neuron degeneration
SLH Shing, J Lope, MC McKenna, RH Chipika… - Journal of the …, 2021 - Elsevier
Background Post-polio syndrome (PPS) has been traditionally considered a slowly
progressive condition that affects poliomyelitis survivors decades after their initial infection …
progressive condition that affects poliomyelitis survivors decades after their initial infection …
[HTML][HTML] Progressive brainstem pathology in motor neuron diseases: imaging data from amyotrophic lateral sclerosis and primary lateral sclerosis
A standardised, single-centre, longitudinal imaging protocol was used to evaluate
longitudinal brainstem alterations in 100 patients with amyotrophic lateral sclerosis (ALS) …
longitudinal brainstem alterations in 100 patients with amyotrophic lateral sclerosis (ALS) …
The integrity of the corticospinal tract and corpus callosum, and the risk of ALS: univariable and multivariable Mendelian randomization
J Wu, G Zhang, L Zhang, S Ye, T Huang, D Fan - Scientific Reports, 2024 - nature.com
Studies suggest that amyotrophic lateral sclerosis (ALS) compromises the integrity of white
matter fiber tracts, primarily affecting motor fibers. However, it remains uncertain whether the …
matter fiber tracts, primarily affecting motor fibers. However, it remains uncertain whether the …
[HTML][HTML] Cerebellar remodelling decades after spinal cord insult: neuroplasticity in poliomyelitis survivors
SLH Shing, A Murad, J Lope, O Hardiman… - Journal of Integrative …, 2022 - imrpress.com
Background: The cerebellum integrates a multitude of motor and cognitive processes
through ample spinal and supratentorial projections. Despite emerging evidence of adaptive …
through ample spinal and supratentorial projections. Despite emerging evidence of adaptive …
Extra-motor manifestations in post-polio syndrome (PPS): fatigue, cognitive symptoms and radiological features
S Li Hi Shing, J Lope, RH Chipika, O Hardiman… - Neurological …, 2021 - Springer
Background There is a paucity of cerebral neuroimaging studies in post-polio syndrome
(PPS), despite the severity of neurological and neuropsychological sequelae associated …
(PPS), despite the severity of neurological and neuropsychological sequelae associated …
[HTML][HTML] Imaging and clinical data indicate considerable disease burden in 'probable'PLS: Patients with UMN symptoms for 2–4 years
E Finegan, WF Siah, SLH Shing, RH Chipika… - Data in brief, 2020 - Elsevier
Primary lateral sclerosis (PLS) is an adult-onset upper motor neuron disease manifesting in
progressive spasticity and gradually resulting in considerably motor disability. In the …
progressive spasticity and gradually resulting in considerably motor disability. In the …
Update on recent advances in amyotrophic lateral sclerosis
In the last few years, our understanding of disease molecular mechanisms underpinning
ALS has advanced greatly, allowing the first steps in translating into clinical practice novel …
ALS has advanced greatly, allowing the first steps in translating into clinical practice novel …
Language deficits in primary lateral sclerosis: cortical atrophy, white matter degeneration and functional disconnection between cerebral regions
EL Tan, M Tahedl, J Lope, JC Hengeveld… - Journal of …, 2024 - Springer
Background Primary lateral sclerosis (PLS) is traditionally regarded as a pure upper motor
neuron disorder, but recent cases series have highlighted cognitive deficits in executive and …
neuron disorder, but recent cases series have highlighted cognitive deficits in executive and …
Current challenges in primary lateral sclerosis diagnosis
M Oliveira Santos, M Swash… - Expert Review of …, 2024 - Taylor & Francis
Introduction Primary lateral sclerosis (PLS) is a rare, adult-onset and slowly progressive
motor neuron disorder whose clinical core is characterized by upper motor neuron (UMN) …
motor neuron disorder whose clinical core is characterized by upper motor neuron (UMN) …
The involvement of language‐associated networks, tracts, and cortical regions in frontotemporal dementia and amyotrophic lateral sclerosis: Structural and functional …
M Tahedl, EL Tan, RH Chipika, J Lope… - Brain and …, 2023 - Wiley Online Library
Background Language deficits are cardinal manifestations of some frontotemporal dementia
(FTD) phenotypes and also increasingly recognized in sporadic and familial amyotrophic …
(FTD) phenotypes and also increasingly recognized in sporadic and familial amyotrophic …