Amyotrophic lateral sclerosis: a neurodegenerative disorder poised for successful therapeutic translation

RJ Mead, N Shan, HJ Reiser, F Marshall… - Nature Reviews Drug …, 2023 - nature.com
Amyotrophic lateral sclerosis (ALS) is a devastating disease caused by degeneration of
motor neurons. As with all major neurodegenerative disorders, development of disease …

Current state and future directions in the therapy of ALS

L Tzeplaeff, S Wilfling, MV Requardt, M Herdick - Cells, 2023 - mdpi.com
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive neurodegenerative disorder
affecting upper and lower motor neurons, with death resulting mainly from respiratory failure …

Neurofilament light chain in drug development for amyotrophic lateral sclerosis: a critical appraisal

M Benatar, J Wuu, MR Turner - Brain, 2023 - academic.oup.com
Interest in amyotrophic lateral sclerosis (ALS) biomarkers has grown exponentially over the
course of the last 25 years, with great hope that they might serve as tools to facilitate the …

Advances in molecular pathology, diagnosis, and treatment of amyotrophic lateral sclerosis

H Ilieva, M Vullaganti, J Kwan - bmj, 2023 - bmj.com
Although the past two decades have produced exciting discoveries in the genetics and
pathology of amyotrophic lateral sclerosis (ALS), progress in developing an effective therapy …

[HTML][HTML] Update on the epidemiology, pathogenesis, and biomarkers of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

Y Yamamoto, YC Liao, YC Lee, M Ihara… - Journal of Clinical …, 2023 - ncbi.nlm.nih.gov
Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) is the most common monogenic disorder of the cerebral …

Proteomics and mathematical modeling of longitudinal CSF differentiates fast versus slow ALS progression

L Vu, K Garcia‐Mansfield, A Pompeiano… - Annals of clinical …, 2023 - Wiley Online Library
Objective Amyotrophic lateral sclerosis (ALS) is a heterogeneous disease with a complex
etiology that lacks biomarkers predicting disease progression. The objective of this study …

Can we use blood biomarkers as entry criteria and for monitoring drug treatment effects in clinical trials? A report from the EU/US CTAD task force

D Angioni, O Hansson, RJ Bateman, C Rabe… - The Journal of …, 2023 - Springer
In randomized clinical trials (RCTs) for Alzheimer's Disease (AD), cerebrospinal fluid (CSF)
and positron emission tomography (PET) biomarkers are currently used for the detection …

Studies to assess the utility of serum neurofilament light chain as a biomarker in chemotherapy-induced peripheral neuropathy

G Cavaletti, C Pizzamiglio, A Man, TM Engber, C Comi… - Cancers, 2023 - mdpi.com
Simple Summary Since neuroaxonal damage and loss are observed in chemotherapy-
induced peripheral neuropathy (CIPN) and results in permanent disability, detecting and …

Serum neurofilament light chain and initial severity of neurological disease predict the early neurological deterioration in Wilson's disease

T Ziemssen, L Smolinski, A Członkowska… - Acta Neurologica …, 2023 - Springer
Abstract Background In Wilson's disease (WD), early neurological deterioration after
treatment initiation is associated with poor outcomes; however, data on this phenomenon …

Phenotypic correlates of serum neurofilament light chain levels in amyotrophic lateral sclerosis

F Verde, I Milone, E Colombo, A Maranzano… - Frontiers in Aging …, 2023 - frontiersin.org
Objective To investigate the relationship between serum levels of the neuroaxonal
degeneration biomarker neurofilament light chain (NFL) and phenotype in ALS. Materials …