[HTML][HTML] The role of VCP mutations in the Spectrum of amyotrophic lateral sclerosis—frontotemporal dementia

E Scarian, G Fiamingo, L Diamanti, I Palmieri… - Frontiers in …, 2022 - frontiersin.org
Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD) are two
neurological diseases which, respectively, and primarily affect motor neurons and …

[HTML][HTML] Diffusion tensor imaging in amyotrophic lateral sclerosis: machine learning for biomarker development

A Behler, HP Müller, AC Ludolph… - International journal of …, 2023 - mdpi.com
Diffusion tensor imaging (DTI) allows the in vivo imaging of pathological white matter
alterations, either with unbiased voxel-wise or hypothesis-guided tract-based analysis …

[HTML][HTML] Lipidomics study of plasma from patients suggest that ALS and PLS are part of a continuum of motor neuron disorders

E Area-Gomez, D Larrea, T Yun, Y Xu, J Hupf… - Scientific reports, 2021 - nature.com
Motor neuron disorders (MND) include a group of pathologies that affect upper and/or lower
motor neurons. Among them, amyotrophic lateral sclerosis (ALS) is characterized by …

Adaptive functional reorganization in amyotrophic lateral sclerosis: coexisting degenerative and compensatory changes

M Abidi, G de Marco, A Couillandre… - European Journal of …, 2020 - Wiley Online Library
Background and purpose Considerable functional reorganization takes place in
amyotrophic lateral sclerosis (ALS) in face of relentless structural degeneration. This study …

[HTML][HTML] Development and validation of a 1-year survival prognosis estimation model for Amyotrophic Lateral Sclerosis using manifold learning algorithm UMAP

V Grollemund, GL Chat, MS Secchi-Buhour, F Delbot… - Scientific reports, 2020 - nature.com
Abstract Amyotrophic Lateral Sclerosis (ALS) is an inexorably progressive
neurodegenerative condition with no effective disease modifying therapies. The …

[HTML][HTML] Pathological neural networks and artificial neural networks in ALS: diagnostic classification based on pathognomonic neuroimaging features

P Bede, A Murad, O Hardiman - Journal of neurology, 2021 - Springer
The description of group-level, genotype-and phenotype-associated imaging traits is
academically important, but the practical demands of clinical neurology centre on the …

Hippocampal pathology in amyotrophic lateral sclerosis: selective vulnerability of subfields and their associated projections

F Christidi, E Karavasilis, M Rentzos, G Velonakis… - Neurobiology of …, 2019 - Elsevier
Although hippocampal involvement in amyotrophic lateral sclerosis (ALS) has been
consistently highlighted by postmortem studies, memory impairment remains under …

The clinical and radiological profile of primary lateral sclerosis: a population-based study

E Finegan, RH Chipika, S Li Hi Shing, MA Doherty… - Journal of …, 2019 - Springer
Background Primary lateral sclerosis is a progressive upper-motor-neuron disorder
associated with markedly longer survival than ALS. In contrast to ALS, the genetic …

[HTML][HTML] Tracking a fast-moving disease: longitudinal markers, monitoring, and clinical trial endpoints in ALS

RH Chipika, E Finegan, S Li Hi Shing… - Frontiers in …, 2019 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) encompasses a heterogeneous group of phenotypes
with different progression rates, varying degree of extra-motor involvement and divergent …

[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 …