Current drug repurposing strategies for rare neurodegenerative disorders

S Shah, MM Dooms, S Amaral-Garcia… - Frontiers in …, 2021 - frontiersin.org
Rare diseases are life-threatening or chronically debilitating low-prevalent disorders caused
by pathogenic mutations or particular environmental insults. Due to their high complexity …

[HTML][HTML] Diagnosis and differential diagnosis of MND/ALS: IFCN handbook chapter

M de Carvalho, M Swash - Clinical Neurophysiology Practice, 2024 - Elsevier
Accurate and rapid diagnosis of amyotrophic lateral sclerosis (ALS) is essential in order to
provide accurate information for patient and family, to avoid time-consuming investigations …

[HTML][HTML] Drug repurposing: a network-based approach to amyotrophic lateral sclerosis

G Fiscon, F Conte, S Amadio, C Volonté, P Paci - Neurotherapeutics, 2021 - Elsevier
The continuous adherence to the conventional “one target, one drug” paradigm has failed so
far to provide effective therapeutic solutions for heterogeneous and multifactorial diseases …

Regional spreading pattern is associated with clinical phenotype in amyotrophic lateral sclerosis

A Maranzano, F Verde, E Colombo, B Poletti, A Doretti… - Brain, 2023 - academic.oup.com
Increasing evidence shows that disease spreading in amyotrophic lateral sclerosis (ALS)
follows a preferential pattern with more frequent involvement of contiguous regions from the …

TDP-43 differentially propagates to induce antero-and retrograde degeneration in the corticospinal circuits in mouse focal ALS models

S Tsuboguchi, Y Nakamura, T Ishihara, T Kato… - Acta …, 2023 - Springer
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease
characterized by TDP-43 inclusions in the cortical and spinal motor neurons. It remains …

BDNF and pro-BDNF in amyotrophic lateral sclerosis: a new perspective for biomarkers of neurodegeneration

G Riolo, C Ricci, N De Angelis, C Marzocchi… - Brain Sciences, 2022 - mdpi.com
Amyotrophic Lateral Sclerosis (ALS) is characterized by the progressive degeneration of
upper or lower motor neurons, leading to muscle wasting and paralysis, resulting in …

Different patterns of spreading direction and motor neurons involvement in a cohort of limb‐onset amyotrophic lateral sclerosis patients from Southern Italy: Potential …

G Milella, S Zoccolella, D Urso, S Nigro… - Brain and …, 2023 - Wiley Online Library
Background Currently, there is a lack of knowledge concerning where the pathological
process starts and how the neurodegeneration spreads during the course of amyotrophic …

Clinical spreading of muscle weakness in amyotrophic lateral sclerosis (ALS): a study in 910 patients

AC Ludolph, J Dietrich, J Dreyhaupt, J Kassubek… - Journal of …, 2024 - Springer
Background Neuroanatomical staging of sporadic amyotrophic lateral sclerosis (ALS)
indicates that neurodegeneration may spread corticofugally. Methods We conducted an …

Use of hip-versus wrist-based actigraphy for assessing functional decline and disease progression in patients with motor neuron disease

CJ Holdom, JWJ van Unnik, RPA van Eijk… - Journal of …, 2023 - Springer
Background Actigraphy has been proposed as a measure for tracking functional decline and
disease progression in patients with Motor Neuron Disease (MND). There is, however, little …

Spatial–temporal pattern of propagation in amyotrophic lateral sclerosis and effect on survival: A cohort study

T Yang, Q Wei, C Li, B Cao, R Ou, Y Hou… - European Journal of …, 2022 - Wiley Online Library
Background and purpose Clarification of propagation patterns in amyotrophic lateral
sclerosis (ALS) is challenging, but understanding these has implications for individual …