Hypermetabolism in ALS is associated with greater functional decline and shorter survival

FJ Steyn, ZA Ioannides, RPA Van Eijk… - Journal of Neurology …, 2018 - jnnp.bmj.com
Objective To determine the prevalence of hypermetabolism, relative to body composition, in
amyotrophic lateral sclerosis (ALS) and its relationship with clinical features of disease and …

[HTML][HTML] Assessment of motor units in neuromuscular disease

RD Henderson, PA McCombe - Neurotherapeutics, 2017 - Elsevier
The motor unit comprises the anterior horn cell, its axon, and the muscle fibers that it
innervates. Although the true number of motor units is unknown, the number of motor units …

Connectome‐based propagation model in amyotrophic lateral sclerosis

JM Meier, HK van Der Burgh, AD Nitert… - Annals of …, 2020 - Wiley Online Library
Objective Clinical trials in amyotrophic lateral sclerosis (ALS) continue to rely on survival or
functional scales as endpoints, despite the emergence of quantitative biomarkers …

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 …

Ghrelin as a treatment for amyotrophic lateral sclerosis

ST Ngo, H Wang, RD Henderson… - Journal of …, 2021 - Wiley Online Library
Ghrelin is a gut hormone best known for its role in regulating appetite and stimulating the
secretion of the anabolic hormone growth hormone (GH). However, there is considerable …

[HTML][HTML] 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 …

Serum levels of glial fibrillary acidic protein in patients with amyotrophic lateral sclerosis

F Verde, I Milone, A Maranzano… - Annals of Clinical …, 2023 - Wiley Online Library
Objective To compare serum levels of the astrocyte biomarker glial fibrillary acidic protein
(GFAP) in patients with amyotrophic lateral sclerosis (ALS) and neurologically healthy …

[HTML][HTML] Motor, cognitive and behavioural profiles of C9orf72 expansion-related amyotrophic lateral sclerosis

E Colombo, B Poletti, A Maranzano, S Peverelli… - Journal of …, 2023 - Springer
Introduction Amyotrophic lateral sclerosis (ALS) individuals carrying the hexanucleotide
repeat expansion (HRE) in the C9orf72 gene (C9Pos) have been described as presenting …

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 …

Severity of in vivo corticospinal tract degeneration is associated with survival in amyotrophic lateral sclerosis: a longitudinal, multicohort study

D Ta, AH Ishaque, A Elamy, T Anand… - European Journal of …, 2023 - Wiley Online Library
Background and purpose This study sought to evaluate the relationship of progressive
corticospinal tract (CST) degeneration with survival in patients with amyotrophic lateral …