Disease: Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1
- A Novel De Novo Missense Mutation in KIF1A Associated with Young-Onset Upper-Limb Amyotrophic Lateral Sclerosis
- A patient-derived amyotrophic lateral sclerosis blood-brain barrier model for focused ultrasound-mediated anti-TDP-43 antibody delivery
- Abnormal Splicing Events due to Loss of Nuclear Function of TDP-43: Pathophysiology and Perspectives
- All-in-one wearable drug efficacy assessment systems for bulbar muscle function using amyotrophic lateral sclerosis animal models
- Allele-Selective Thiomorpholino Antisense Oligonucleotides as a Therapeutic Approach for Fused-in-Sarcoma Amyotrophic Lateral Sclerosis
- ALS-FUS mutations cause abnormal PARylation and histone H1.2 interaction, leading to pathological changes
- Amyotrophic Lateral Sclerosis (ALS): An Overview of Genetic and Metabolic Signaling Mechanisms
- Amyotrophic lateral sclerosis associated with a new pathogenic variant of the ERBB4 gene
- An Accurate and Rapidly Calibrating Speech Neuroprosthesis
- An automatic measure for speech intelligibility in dysarthrias-validation across multiple languages and neurological disorders
- Anesthetic Management of a Neurosurgical Patient With Amyotrophic Lateral Sclerosis: A Case Report
- Bulbar muscle impairment in patients with late onset Pompe disease: Insight from the French Pompe registry
- Causal relationship between imaging-derived phenotypes and neurodegenerative diseases: a Mendelian randomization study
- Central neurodegeneration in Kennedy's disease accompanies peripheral motor dysfunction
- CHCHD2 P14L, found in amyotrophic lateral sclerosis, exhibits cytoplasmic mislocalization and alters Ca(2+) homeostasis
- Circulating endocannabinoidome signatures of disease activity in amyotrophic lateral sclerosis
- Circulating MAIT cells in multiple sclerosis and amyotrophic lateral sclerosis
- Clinical characterization of common pathogenic variants of SOD1-ALS in Germany
- Coffee and amyotrophic lateral sclerosis (ALS)
- Coffee, antioxidants, and brain inflammation
- Comparative assessment of MScanFit MUNE and quantitative EMG in amyotrophic lateral sclerosis diagnosis: A prospective study
- Compassionate Ventilator Release In Patients With Neuromuscular Disease: A Two-Case Comparison
- Cortical inexcitability in ALS: correlating a clinical phenotype
- Cortical microstructural abnormalities in amyotrophic lateral sclerosis: a gray matter-based spatial statistics study
- CSF Neopterin Levels Are Elevated in Various Neurological Diseases and Aging
- Current progress in microRNA profiling of circulating extracellular vesicles in amyotrophic lateral sclerosis: A systematic review
- Current status and new avenues of stem cell-based preclinical and therapeutic approaches in amyotrophic lateral sclerosis
- D-Glutamate production by stressed Escherichia coli gives a clue for the hypothetical induction mechanism of the ALS disease
- Data and Process Harmonisation of Multi-National, Multi-Site Research Data
- Development and Piloting of a Bereaved Care Partner Survey to Inform Quality Improvement in ALS Supportive Care
- Diagnostic elements in amyotrophic lateral sclerosis: A case report
- Different baseline functional patterns of the frontal cortex in amyotrophic lateral sclerosis patients with Corticospinal tract hyperintensity
- Dilemma in patients with amyotrophic lateral sclerosis and expectations from brain-machine interfaces
- Diverse Phenotypic Presentation of the Welander Distal Myopathy Founder Mutation, With Myopathy and Amyotrophic Lateral Sclerosis in the Same Family
- DNAJA2 and Hero11 mediate similar conformational extension and aggregation suppression of TDP-43
- Electrodiagnostic support in an atypical form of amyotrophic lateral sclerosis (Vulpian-Bernhardt syndrome)
- Electrografted Laser-Induced Graphene: Direct Detection of Neurodegenerative Disease Biomarker in Cerebrospinal Fluid
- Excitotoxicity, Oxytosis/Ferroptosis, and Neurodegeneration: Emerging Insights into Mitochondrial Mechanisms
- Exploring the Impact of Amyotrophic Lateral Sclerosis on Otolaryngological Functions
- Factors associated with Edinburgh Cognitive and Behavioural ALS Screen (ECAS) alteration at time of diagnosis, in amyotrophic lateral sclerosis
- Fatty links between multisystem proteinopathy and small VCP-interacting protein
- Friend or foe: Lactate in neurodegenerative diseases
- Genotype-phenotype correlation of SQSTM1 variants in patients with amyotrophic lateral sclerosis
- Harnessing transcriptomic signals for amyotrophic lateral sclerosis to identify novel drugs and enhance risk prediction
- HDAC6 inhibition as a mechanism to prevent neurodegeneration in the mSOD1<sup>G93A</sup> mouse model of ALS
- Hybrid derivatives containing dimethyl fumarate and benzothiazole scaffolds for the potential treatment of multiple sclerosis; in silico & in vivo study
- Identification of human metabolites of fast skeletal troponin activators Tirasemtiv and Reldesemtiv for doping control purposes
- Identification of potential drug targets for amyotrophic lateral sclerosis by Mendelian randomization analysis based on brain and plasma proteomics
- Inhibition of glycolytic reprogramming suppresses innate immune-mediated inflammation in experimental amyotrophic lateral sclerosis
- Inhibition of PHLDA3 expression in human superoxide dismutase 1-mutant amyotrophic lateral sclerosis astrocytes protects against neurotoxicity
- Intranasal delivery of small extracellular vesicles reduces the progress of amyotrophic lateral sclerosis and the overactivation of complement-coagulation cascade and NF-qB signaling in SOD1(G93A) mice
- Klotho: molecular mechanisms and emerging therapeutics in central nervous system diseases
- Lingual Fasciculation as a Point of Call for the Diagnosis of Amyotrophic Lateral Sclerosis: A Literature Review
- Longevity of a Brain-Computer Interface for Amyotrophic Lateral Sclerosis
- Low-intensity pulsed ultrasound modulates disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis
- LPA3 agonist-producing Bacillus velezensis ADS024 is efficacious in multiple neuroinflammatory disease models
- Mass spectrometry imaging of SOD1 protein-metal complexes in SOD1G93A transgenic mice implicates demetalation with pathology
- Mitochondrial Dysfunction is a Crucial Immune Checkpoint for Neuroinflammation and Neurodegeneration: mtDAMPs in Focus
- Mitochondrial genome variants associated with amyotrophic lateral sclerosis and their haplogroup distribution
- Molecular mechanisms and antisense oligonucleotide therapies of familial amyotrophic lateral sclerosis
- Morphometric analysis of spinal motor neuron degeneration in sporadic amyotrophic lateral sclerosis
- Multimodal speech biomarkers for remote monitoring of ALS disease progression
- Multiple metal exposures associate with higher amyotrophic lateral sclerosis risk and mortality independent of genetic risk and correlate to self-reported exposures: a case-control study
- Novel multitarget directed ligands inspired by riluzole: A serendipitous synthesis of substituted benzo[b][1,4]thiazepines potentially useful as neuroprotective agents
- Overexpression of Toxic Poly(Glycine-Alanine) Aggregates in Primary Neuronal Cultures Induces Time-Dependent Autophagic and Synaptic Alterations but Subtle Activity Impairments
- Patient-Reported Impact of Symptoms in Spinal and Bulbar Muscular Atrophy
- Physical exercise in amyotrophic lateral sclerosis: a potential co-adjuvant therapeutic option to counteract disease progression
- Poly-GR Impairs PRMT1-Mediated Arginine Methylation of Disease-Linked RNA-Binding Proteins by Acting as a Substrate Sink
- Poly-GR repeats associated with ALS/FTD gene <em>C9ORF72</em> impair translation elongation and induce a ribotoxic stress response in neurons
- Population-Based Evidence for the Use of Serum Neurofilaments as Individual Diagnostic and Prognostic Biomarkers in Amyotrophic Lateral Sclerosis
- Postmovement Beta Rebound in Real and Imagined Movement
- Promising animal models for amyotrophic lateral sclerosis drug discovery: a comprehensive update
- Prostaglandins in the Inflamed Central Nervous System: Potential Therapeutic Targets
- Psychiatric Manifestations of Neurological Diseases: A Narrative Review
- RBM5 induces motor neuron apoptosis in hSOD1(G93A)-related amyotrophic lateral sclerosis by inhibiting Rac1/AKT pathways
- Schwann cell JUN expression worsens motor performance in an amyotrophic lateral sclerosis mouse model
- Scientific plurality and amyotrophic lateral sclerosis (ALS): A philosophical and historical perspective on Charcot's texts
- Sigma-1 receptor recruits LC3 mRNA to ER-associated omegasomes to promote localized LC3 translation enabling functional autophagy
- Simultaneous time-frequency analysis of gait signals of both legs in classifying neurodegenerative diseases
- Small Molecule Inhibitors of Arylamine N-Acetyltransferase 1 Attenuate Cellular Respiration
- SoDCoD: a comprehensive database of Cu/Zn superoxide dismutase conformational diversity caused by ALS-linked gene mutations and other perturbations
- Sonography of muscles : Rheumatology-Neurology-Geriatrics-Sports medicine-Orthopedics
- Stress granule formation helps to mitigate neurodegeneration
- Structural basis for RNA recognition by the C-terminal RRM domain of human RBM45
- TBK1 p.Y153Qfs*9 variant may be associated with young-onset, rapidly progressive amyotrophic lateral sclerosis through a haploinsufficiency mechanism
- TDP-43 dysfunction leads to bioenergetic failure and lipid metabolic rewiring in human cells
- The ALS-associated KIF5A P986L variant is not pathogenic for Drosophila motoneurons
- The Evolving Use of Gold Nanoparticles as a Possible Reversal Agent for the Symptoms of Neurodegenerative Diseases: A Narrative Review
- The prion-like effect and prion-like protein targeting strategy in amyotrophic lateral sclerosis
- The role of biomolecular condensates in protein aggregation
- The role of interferon beta in neurological diseases and its potential therapeutic relevance
- The role of macrophage plasticity in neurodegenerative diseases
- The speed of completion of the decremental responses on repetitive nerve stimulation
- Timeline of hypoglossal motor neuron death and intrinsic tongue muscle denervation in high-copy number SOD1<sup>G93A</sup> mice
- Unlocking the therapeutic potential of P2X7 receptor: a comprehensive review of its role in neurodegenerative disorders
- Unraveling mitochondrial dysfunction: comprehensive perspectives on its impact on neurodegenerative diseases
- User expectations and experiences of an assistive robotic arm in amyotrophic lateral sclerosis: a multicenter observational study
- Utility of the Repetitive Nerve Stimulation Test and Needle EMG in the Trapezius Muscle for the Early Diagnosis of ALS
- VAP-mediated membrane-tethering mechanisms implicate ER-PM contact function in pH homeostasis
- VPS35 or retromer as a potential target for neurodegenerative disorders: barriers to progress