Neuroimaging in primary lateral sclerosis

EP Pioro, MR Turner, P Bede - Amyotrophic Lateral Sclerosis and …, 2020 - Taylor & Francis
Increased interest in the underlying pathogenesis of primary lateral sclerosis (PLS) and its
relationship to amyotrophic lateral sclerosis (ALS) has corresponded to a growing number of …

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 …

[HTML][HTML] Amygdala pathology in amyotrophic lateral sclerosis and primary lateral sclerosis

RH Chipika, F Christidi, E Finegan, SLH Shing… - Journal of the …, 2020 - Elsevier
Temporal lobe studies in motor neuron disease overwhelmingly focus on white matter
alterations and cortical grey matter atrophy. Reports on amygdala involvement are …

[HTML][HTML] Extra-motor cerebral changes and manifestations in primary lateral sclerosis

E Finegan, SLH Shing, RH Chipika, KM Chang… - Brain imaging and …, 2021 - Springer
Primary lateral sclerosis (PLS) is classically considered a 'pure'upper motor neuron disorder.
Motor cortex atrophy and pyramidal tract degeneration are thought to be pathognomonic of …

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 …

The secretome of human dental pulp stem cells and its components GDF15 and HB-EGF protect amyotrophic lateral sclerosis motoneurons against death

R Younes, Y Issa, N Jdaa, B Chouaib, V Brugioti… - Biomedicines, 2023 - mdpi.com
Amyotrophic lateral sclerosis (ALS) is a fatal and incurable paralytic disorder caused by the
progressive death of upper and lower motoneurons. Although numerous strategies have …

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 …

Guideline “motor neuron diseases” of the German Society of Neurology (deutsche Gesellschaft für Neurologie)

S Petri, T Grehl, J Grosskreutz, M Hecht… - … Research and Practice, 2023 - Springer
Abstract Introduction In 2021, the Deutsche Gesellschaft für Neurology published a new
guideline on diagnosis and therapy of motor neuron disorders. Motor neuron disorders affect …

[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] Evolving diagnostic criteria in primary lateral sclerosis: the clinical and radiological basis of “probable PLS”

E Finegan, SLH Shing, WF Siah, RH Chipika… - Journal of the …, 2020 - Elsevier
Introduction Primary lateral sclerosis is a rare neurodegenerative disorder of the upper
motor neurons. Diagnostic criteria have changed considerably over the years, and the …