Proteome analysis of body fluids for amyotrophic lateral sclerosis biomarker discovery

T Krüger, J Lautenschläger… - PROTEOMICS …, 2013 - Wiley Online Library
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder of motor
neurons leading to death of the patients, mostly within 2–5 years after disease onset. The …

Serum neurofilament light chain at time of diagnosis is an independent prognostic factor of survival in amyotrophic lateral sclerosis

E Thouvenot, C Demattei, S Lehmann… - European Journal of …, 2020 - Wiley Online Library
Background and purpose The prognostic value of serum neurofilament light chain (sNfL), a
biomarker of neurodegeneration, compared to other prognostic factors of amyotrophic lateral …

[HTML][HTML] Combined tissue-fluid proteomics to unravel phenotypic variability in amyotrophic lateral sclerosis

E Leoni, M Bremang, V Mitra, I Zubiri, S Jung, CH Lu… - Scientific Reports, 2019 - nature.com
The lack of biomarkers for early diagnosis, clinical stratification and to monitor treatment
response has hampered the development of new therapies for amyotrophic lateral sclerosis …

Blood biomarkers in ALS: Challenges, applications and novel frontiers

E Sturmey, A Malaspina - Acta Neurologica Scandinavica, 2022 - Wiley Online Library
Amyotrophic lateral sclerosis (ALS) is the most common motor neuron disease among
adults. With diagnosis reached relatively late into the disease process, extensive motor cell …

Biomarkers in amyotrophic lateral sclerosis: opportunities and limitations

R Bowser, MR Turner, J Shefner - Nature Reviews Neurology, 2011 - nature.com
Insights into the mechanisms of amyotrophic lateral sclerosis (ALS) have relied
predominantly on the study of postmortem tissue. Modern technology has improved the …

Comparison of elevated phosphorylated neurofilament heavy chains in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis

M De Schaepdryver, A Jeromin, B Gille… - Journal of Neurology …, 2018 - jnnp.bmj.com
Objective Phosphorylated neurofilament heavy chain (pNfH) levels are elevated in
cerebrospinal fluid (CSF) of patients with amyotrophic lateral sclerosis (ALS). Instead of …

[HTML][HTML] Decreased levels of foldase and chaperone proteins are associated with an early-onset amyotrophic lateral sclerosis

M Filareti, S Luotti, L Pasetto, M Pignataro… - Frontiers in Molecular …, 2017 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by a
progressive upper and lower motor neuron degeneration. One of the peculiar clinical …

Diagnostic and prognostic value of CSF neurofilaments in a cohort of patients with motor neuron disease: a cross‐sectional study

D Gagliardi, I Faravelli, M Meneri… - Journal of Cellular …, 2021 - Wiley Online Library
Motor neuron disease (MND) is a rare group of disorders characterized by degeneration of
motor neurons (MNs). The most common form of MND, amyotrophic lateral sclerosis (ALS) …

[HTML][HTML] Serum neurofilaments in motor neuron disease and their utility in differentiating ALS, PMA and PLS

G McCluskey, KE Morrison, C Donaghy, J McConville… - Life, 2023 - mdpi.com
Neurofilament levels are elevated in many neurodegenerative diseases and have shown
promise as diagnostic and prognostic biomarkers in Amyotrophic Lateral Sclerosis (ALS) …

[HTML][HTML] Current application of neurofilaments in amyotrophic lateral sclerosis and future perspectives

YM Falzone, T Russo, T Domi, L Pozzi… - Neural Regeneration …, 2021 - journals.lww.com
Motor neuron disease includes a heterogeneous group of relentless progressive
neurological disorders defined and characterized by the degeneration of motor neurons …