Amyotrophic lateral sclerosis

EL Feldman, SA Goutman, S Petri, L Mazzini… - The Lancet, 2022 - thelancet.com
Amyotrophic lateral sclerosis is a fatal CNS neurodegenerative disease. Despite intensive
research, current management of amyotrophic lateral sclerosis remains suboptimal from …

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 …

Pharmacotherapy for amyotrophic lateral sclerosis: a review of approved and upcoming agents

SA Johnson, T Fang, F De Marchi, D Neel… - Drugs, 2022 - Springer
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive neurodegenerative disorder
involving loss of upper and lower motor neurons, with most cases ending in death within 3–5 …

Searching for peripheral biomarkers in neurodegenerative diseases: the tryptophan-kynurenine metabolic pathway

N Török, M Tanaka, L Vécsei - International journal of molecular sciences, 2020 - mdpi.com
Neurodegenerative diseases are multifactorial, initiated by a series of the causative complex
which develops into a certain clinical picture. The pathogenesis and disease course vary …

Exploring the etiological links behind neurodegenerative diseases: Inflammatory cytokines and bioactive kynurenines

M Tanaka, J Toldi, L Vécsei - International Journal of Molecular Sciences, 2020 - mdpi.com
Alzheimer's disease (AD) and Parkinson's disease (PD) are the most common
neurodegenerative diseases (NDs), presenting a broad range of symptoms from motor …

Motor neuron susceptibility in ALS/FTD

AMG Ragagnin, S Shadfar, M Vidal… - Frontiers in …, 2019 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by the
death of both upper and lower motor neurons (MNs) in the brain, brainstem and spinal cord …

Genetics of amyotrophic lateral sclerosis

JM Gregory, D Fagegaltier, H Phatnani… - Current Genetic Medicine …, 2020 - Springer
Abstract Purpose of Review Amyotrophic lateral sclerosis and frontotemporal dementia (ALS-
FTD) spectrum disorder is a rare fatal disease with strong genetic influences. The …

Sensory neuropathy in amyotrophic lateral sclerosis: a systematic review

A Bombaci, A Lupica, FE Pozzi, G Remoli, U Manera… - Journal of …, 2023 - Springer
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by
the degeneration of both upper and lower motoneurons, leading to motor and non-motor …

Non-motor symptoms in amyotrophic lateral sclerosis: lessons from Parkinson's disease

A Shojaie, S Rota, A Al Khleifat… - … Lateral Sclerosis and …, 2023 - Taylor & Francis
Amyotrophic lateral sclerosis and Parkinson's disease are neurodegenerative diseases of
the motor system which are now recognized also to affect non-motor pathways. Non-motor …

A systematic review of non-motor symptom evaluation in clinical trials for amyotrophic lateral sclerosis

E Beswick, D Forbes, Z Hassan, C Wong, J Newton… - Journal of …, 2022 - Springer
Background Amyotrophic lateral sclerosis (ALS) is increasingly recognised as a multi-
system disorder, presenting with common and impactful non-motor symptoms, such as …