Disease: Amyotrophic lateral sclerosis
- 14-3-3θ, a novel player in TDP-43 pathophysiology: Implications for ALS/FTD
- A causal association between amyotrophic lateral sclerosis and atrial fibrillation: a two-sample Mendelian randomization study
- A guide to selecting high-performing antibodies for RNA-binding protein TIA1 for use in Western Blot, immunoprecipitation and immunofluorescence
- A Poem About ALS
- A Potential Role of Interleukin-5 in the Pathogenesis and Progression of Amyotrophic Lateral Sclerosis: A New Molecular Perspective
- A single ALS center experience with clinical use of sodium phenylbutyrate-taurursodiol
- A six degrees-of-freedom cable-driven robotic platform for head-neck movement
- AAV-mediated upregulation of VDAC1 rescues the mitochondrial respiration and sirtuins expression in a SOD1 mouse model of inherited ALS
- Abundant transcriptomic alterations in the human cerebellum of patients with a C9orf72 repeat expansion
- ALSUntangled #75: Portable neuromodulation stimulator therapy
- Altered spreading of fast aperiodic brain waves relates to disease duration in Amyotrophic Lateral Sclerosis
- Amyotrophic lateral sclerosis stratification: unveiling patterns with virome, inflammation, and metabolism molecules
- An aberrant fused in sarcoma liquid droplet of amyotrophic lateral sclerosis pathological variant, R495X, accelerates liquid-solid phase transition
- An Overview of the Bodily Awareness Representation and Interoception: Insights and Progress in the Field of Neurorehabilitation Research
- Analysis of Heart Rate Variability in Individuals Affected by Amyotrophic Lateral Sclerosis
- Animal Models of FUS-Proteinopathy: A Systematic Review
- Apilimod dimesylate in C9orf72 amyotrophic lateral sclerosis: a randomized phase 2a clinical trial
- Biomarkers for Managing Neurodegenerative Diseases
- C/EBPβ: A transcription factor associated with the irreversible progression of Alzheimer's disease
- C9ORF72 deficiency results in neurodegeneration in the zebrafish retina
- C9ORF72 hexanucleotide repeat expansion: From ALS and FTD to a broader pathogenic role?
- C9ORF72 patient-derived endothelial cells drive blood-brain barrier disruption and contribute to neurotoxicity
- Capitalizing on Hope: Questionable Marketing Approval and Pricing of a New ALS Drug
- Chinese Translation and Validation of the Center for Neurologic Study Lability Scale
- Choroid plexus enlargement in amyotrophic lateral sclerosis patients and its correlation with clinical disability and blood-CSF barrier permeability
- Coping as a resource to allow for psychosocial adjustment in fatal disease: results from patients with amyotrophic lateral sclerosis
- Deep learning modeling of rare noncoding genetic variants in human motor neurons defines <em>CCDC146</em> as a therapeutic target for ALS
- Designing multitarget ligands for neurodegenerative diseases with improved permeability trough PLGA nanoencapsulation
- Detection of pTDP-43 via routine muscle biopsy: A promising diagnostic biomarker for amyotrophic lateral sclerosis
- Developing a novel immune infiltration-associated mitophagy prediction model for amyotrophic lateral sclerosis using bioinformatics strategies
- Discovery of a novel homozygous SOD1 truncating variant bolsters infantile SOD1 deficiency syndrome
- Dissecting the effect of ALS mutation S375G on the conformational properties and aggregation dynamics of TDP-43<sub>370-375</sub> fragment
- Distinct transcriptomic profile of satellite cells contributes to preservation of neuromuscular junctions in extraocular muscles of ALS mice
- Early Aggregation Mechanism of SOD1<sub>28-38</sub> Based on Force Field Parameter of 5-Cyano-Tryptophan
- Embryonic motor neuron programming factors reactivate immature gene expression and suppress ALS pathologies in postnatal motor neurons
- Emotion recognition in amyotrophic lateral sclerosis in a dynamic environment
- Enhanced Levels of Fractalkine and HSP60 in Cerebrospinal Fluid of Sporadic Amyotrophic Lateral Sclerosis Patients
- Evaluation of carotid Intima-Media Thickness (IMT) in amyotrophic lateral sclerosis disease using ultrasonography
- Exosomes in Vascular/Neurological Disorders and the Road Ahead
- Expanding SPG18 clinical spectrum: autosomal dominant mutation causes complicated hereditary spastic paraplegia in a large family
- Experiences of predictive genetic testing in inherited motor neuron disease: Findings from a qualitative interview study
- Experiences with advance care planning in amyotrophic lateral sclerosis: Qualitative longitudinal study with people with amyotrophic lateral sclerosis and their family carers
- Flavan-3-ols, flavonoids, anthocyanidins and triterpenoids induces TIE2 phosphorylation -a candidate target for the vascular protective effects
- Formation of Supplementary Metal-Binding Centers in Proteins under Stress Conditions
- Gangliosides as Therapeutic Targets for Neurodegenerative Diseases
- Generation and characterization of monoclonal antibodies against pathologically phosphorylated TDP-43
- Genetic diagnosis and detection rates using C9orf72 repeat expansion and a multi-gene panel in amyotrophic lateral sclerosis
- Identification of hub genes and diagnostic efficacy for triple-negative breast cancer through WGCNA and Mendelian randomization
- Identifying the Unmet Needs of People Living With Amyotrophic Lateral Sclerosis: A National Survey to Inform Interdisciplinary Palliative Care
- IgM anti-GM2 antibodies in patients with multifocal motor neuropathy target Schwann cells and are associated with early onset
- Increased Vulnerability to Ferroptosis in FUS-ALS
- Investigating Repeat Expansions in NIPA1, NOP56, and NOTCH2NLC Genes: A Closer Look at Amyotrophic Lateral Sclerosis Patients from Southern Italy
- Investigating the Therapeutics Effects of Oral Cavity Derived Stem Cells on Neurodegenerative Diseases: A Systematic Review
- Involvement of Glucosamine 6 Phosphate Isomerase 2 (GNPDA2) Overproduction in β-Amyloid- and Tau P301L-Driven Pathomechanisms
- Knockdown of <em>tgfb1a</em> partially improves ALS phenotype in a transient zebrafish model
- L-Carnitine in the Treatment of Psychiatric and Neurological Manifestations: A Systematic Review
- LINC complex alterations are a key feature of sporadic and familial ALS/FTD
- Long-timescale atomistic simulations uncover loss-of-function mechanisms of uncharacterized Angiogenin mutants associated with ALS
- Longitudinal Changes in the Retinal Nerve Fiber Layer Thickness in Amyotrophic Lateral Sclerosis and Parkinson's Disease: A Comparative Study
- Longitudinal feasibility of the Montreal Cognitive Assessment (MoCA) in non-demented ALS patients
- Mitochondrial and Nuclear DNA Variants in Amyotrophic Lateral Sclerosis: Enrichment in the Mitochondrial Control Region and Sirtuin Pathway Genes in Spinal Cord Tissue
- Motor band sign is specific for amyotrophic lateral sclerosis and corresponds to motor symptoms
- Nestorone (segesterone acetate) effects on neuroregeneration
- Neurodegeneration Biomarkers in Adult Spinal Muscular Atrophy (SMA) Patients Treated with Nusinersen
- Neurofilaments as biomarkers in neurological disorders - towards clinical application
- Neurofilaments in Sporadic and Familial Amyotrophic Lateral Sclerosis: A Systematic Review and Meta-Analysis
- Neuroinflammation in Neurodegenerative Disorders: Current Knowledge and Therapeutic Implications
- Neurophysiological and imaging biomarkers of lower motor neuron dysfunction in motor neuron diseases/amyotrophic lateral sclerosis: IFCN handbook chapter
- Non-Pharmacological Interventions on Pain in Amyotrophic Lateral Sclerosis Patients: A Systematic Review and Meta-Analysis
- Novel Isoxazolidines as RIPK1 Inhibitors for Treating Alzheimer's Disease, Multiple Sclerosis, and Amyotrophic Lateral Sclerosis
- Online speech synthesis using a chronically implanted brain-computer interface in an individual with ALS
- Optimizing breathlessness management in amyotrophic lateral sclerosis: insights from a comprehensive systematic review
- Optineurin-facilitated axonal mitochondria delivery promotes neuroprotection and axon regeneration
- Origin, identity, and function of terminal Schwann cells
- Pan-neuronal expression of human mutant SOD1 in Drosophila impairs survival and motor performance, induces early neuroinflammation and chromosome aberrations
- Patients' experiences with methylcobalamin injections in amyotrophic lateral sclerosis
- Percutaneous Gastrostomies: Associated Complications in PUSH vs. PULL Techniques over 12 Years in a Referral Centre
- Peripheral extracellular vesicles in neurodegeneration: pathogenic influencers and therapeutic vehicles
- Peripheral Immune Profiles Predict ALS Progression in an Age- and Sex-Dependent Manner
- Practical Three-Component Regioselective Synthesis of Drug-Like 3-Aryl(or heteroaryl)-5,6-dihydrobenzo[<em>h</em>]cinnolines as Potential Non-Covalent Multi-Targeting Inhibitors To Combat Neurodegenerative Diseases
- Protocol to identify DNA-binding proteins recognizing nucleotide repeat dsDNAs
- Rare association between spinocerebellar ataxia and amyotrophic lateral sclerosis: a case series
- Real-time ultrasound-guided sacral plexus block combined with mild sedation for hemorrhoidectomy and hemorrhoidal artery ligation in a patient with amyotrophic lateral sclerosis: a case report
- Reversal of <em>C9orf72</em> mutation-induced transcriptional dysregulation and pathology in cultured human neurons by allele-specific excision
- Revisiting distinct nerve excitability patterns in patients with amyotrophic lateral sclerosis
- Safety of masitinib in patients with neurodegenerative diseases: a meta-analysis of randomized controlled trials
- Smell the smoke before one sees the fire-The oligosymptomatic prodromal phase of neurodegenerative diseases
- SOD1 gene therapy delays ALS disease progression
- Spatial enrichment and genomic analyses reveal the link of NOMO1 with amyotrophic lateral sclerosis
- Structural Investigations on 2-Amidobenzimidazole Derivatives as New Inhibitors of Protein Kinase CK1 Delta
- Testosterone Reduces Myelin Abnormalities in the Wobbler Mouse Model of Amyotrophic Lateral Sclerosis
- Text and image generation from intracranial electroencephalography using an embedding space for text and images
- The Influence of Myeloid-Derived Suppressor Cell Expansion in Neuroinflammation and Neurodegenerative Diseases
- Tissue informative cell-free DNA methylation sites in amyotrophic lateral sclerosis
- Toxic gain-of-function mechanisms in <em>C9orf72</em> ALS-FTD neurons drive autophagy and lysosome dysfunction
- Transient Acute Diplopia as a Rare Side Effect of Hydromorphone: A Case Report
- Treating Alzheimer's disease using nanoparticle-mediated drug delivery strategies/systems
- Two Cases of Sporadic Amyotrophic Lateral Sclerosis With Contrasting Clinical Phenotypes: Genetic Insights
- Two-sample Mendelian randomization analysis of 91 circulating inflammatory protein levels and amyotrophic lateral sclerosis
- Use of Muscle Ultrasonography in Morphofunctional Assessment of Amyotrophic Lateral Sclerosis (ALS)