What researchers published on ALS (motor neurone disease)
2,064 papers, newest first.
Showing 180 of 2,064
Not labelled yetCommunity awareness and knowledge of amyotrophic lateral sclerosis: a cross-sectional study in the Northern Border Region of Saudi Arabia.PeerJ
Not labelled yetCorrespondence- The Unfinished Breath: Caregiver Perceptions of Terminal Events and Gaps in Amyotrophic Lateral Sclerosis Care in India - Methodological Considerations.Annals of Indian Academy of Neurology
ReviewBeyond neurones: cardiac involvement in motor neurone disease.Neuroscience
Not labelled yetAmyotrophic lateral sclerosis treated with the modified Bu-Shen-Jian-Pi decoction (mBSJP): Multicenter study.International journal of clinical pharmacology and therapeutics
PreprintTemporal RNA splicing dysregulation in a human multicellular model of C9orf72 ALS.bioRxiv : the preprint server for biology
PreprintCerebrospinal fluid α-synuclein seed amplification assay positivity identifies a prognostically distinct subgroup in amyotrophic lateral sclerosis.medRxiv : the preprint server for health sciences
Not labelled yetThe decline of respiratory function in amyotrophic lateral sclerosis patients and the role of non-invasive ventilation.Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace
Not labelled yetEfficacy and tolerability of D-β-hydroxybutyrate ester in patients with amyotrophic lateral sclerosis (KETO-ALS)-a randomised, placebo-controlled, double-blind study.EClinicalMedicine
Not labelled yetTDP-43-related cryptic splicing reflects pathological heterogeneity in amyotrophic lateral sclerosis.Acta neuropathologica communications
Not labelled yetA revised motor unit number estimate detects presymptomatic motor neuron loss in amyotrophic lateral sclerosis.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
Not labelled yetProtein Isoaspartate Repair in Amyotrophic Lateral Sclerosis: An Integrative Bioinformatic Analysis of the PCMT Gene Family.ACS chemical neuroscience
Not labelled yetPersonalizing nutritional care in amyotrophic lateral sclerosis (ALS): a multi-perspective qualitative focus group study of experiences and challenges.Amyotrophic lateral sclerosis & frontotemporal degeneration
Not labelled yetSubtype and stage inference of tract-level diffusion abnormalities in amyotrophic lateral sclerosis.Journal of neurology
ReviewCurrent findings, application, and diagnosis of magnetic resonance imaging in amyotrophic lateral sclerosis.Reviews in the neurosciences
Not labelled yetA validated antibody toolbox for ALS research.eLife
Not labelled yetLack of NRF2 expression alters the dynamics of stress granules promoting the aggregation of ALS disease-associated proteins.Redox biology
Not labelled yetUrinary Dysfunction in ALS Patients: Assessment With the Overactive Bladder Awareness Tool.Neurourology and urodynamics
Not labelled yetVoxel-based texture similarity networks reveal abnormal brain network topology linked to molecular signatures in amyotrophic lateral sclerosis.BMC medicine
Not labelled yet[Mitochondria in sporadic amyotrophic lateral sclerosis: actor or initiator?].Medecine sciences : M/S
Not labelled yetThe impact of diagnostic criteria on the detection of nocturnal hypoventilation in adult amyotrophic lateral sclerosis patients.Sleep medicine
Not labelled yetPatient and public involvement in amyotrophic lateral sclerosis research in Japan: a survey through nationally advertised ALS Café events and a pilot advocacy training program.Research involvement and engagement
Not labelled yetStrain-specific morphology and CNS propagation of template-directed SOD1 aggregation following peripheral nerve inoculation.Acta neuropathologica communications
Not labelled yetCorrigendum to From Vision to Validation: The Journey of Tofersen in Superoxide Dismutase 1Gene-Associated Amyotrophic Lateral Sclerosis [Mayo Clinic Proceeding: Innovations, Quality & Outcomes 10(5) (2026) PIQO_100755].Mayo Clinic proceedings. Innovations, quality & outcomes
Not labelled yetImpact of hybrid assistive limb on gait ability and quality of life in patients with amyotrophic lateral sclerosis.Frontiers in neurology
Not labelled yetFeasibility of Longitudinal Home Monitoring of Nocturnal Transcutaneous CO2 and Relationship to Standard Respiratory Measures in Patients With ALS: A Pilot Cohort Study.Muscle & nerve
Not labelled yetCharacterization of plasma misfolded superoxide dismutase 1 in amyotrophic lateral sclerosis.Neurobiology of disease
ReviewBypassing the Blood-Central Nervous System (CNS) Barrier: A Dual-Axis Framework for Amyotrophic Lateral Sclerosis (ALS) Utilizing Glymphatic-Lymphatic Clearance and In Situ Chaperone Synthesis.Cureus
Not labelled yetPersistent and compartmentalized T cell immunity in ALS.Nature medicine
Review[Disease modeling with iPSCs for pathophysiological elucidation and therapeutic research: establishment of an iPSC-based drug discovery platform centered on drug repositioning].[Rinsho ketsueki] The Japanese journal of clinical hematology
Not labelled yetLongitudinal coagulation-fibrinolysis dynamics are associated with survival in amyotrophic lateral sclerosis: a prospective cohort study.Amyotrophic lateral sclerosis & frontotemporal degeneration
Observational studyAnatomically Defined Motor Phenotypes Reveal Dissociated Trajectories of Progression, Neurofilament Profiles, and Survival in ALS.European journal of neurology
Not labelled yetCombined melatonin and edaravone therapy attenuates methylmercury-induced amyotrophic lateral sclerosis-like neurodegeneration through GLP-1 modulation and myelin preservation.Naunyn-Schmiedeberg's archives of pharmacology
Not labelled yetTime-to-Event Analysis of Clinical Milestones in the ALS Natural History Consortium Dataset.Muscle & nerve
Not labelled yetIntracisternal injection of two human SOD1 aggregate strains induces templated aggregation and ALS in transgenic mouse model.Acta neuropathologica communications
Not labelled yetThe cost of mentalizing: executive contributions to social cognition performance in amyotrophic lateral sclerosis.Frontiers in psychology
Not labelled yetNEK1 autophosphorylation is disrupted by amyotrophic lateral sclerosis-associated missense variants: activity biomarkers and structural insights.Open biology
ReviewThe Boron-Neuron Connection: The Potential of Boron-Containing Molecules for Treating Incurable Amyotrophic Lateral Sclerosis.ChemMedChem
ReviewAdvancing the Translational Pipeline: From In Vivo and In Vitro 2D Models to Next-Generation Cell Culture Models for Amyotrophic Lateral Sclerosis Modelling and Drug Discovery.Biomedicines
ReviewThe Role of SOD1 and Oxidative Stress in Amyotrophic Lateral Sclerosis: An Overview.International journal of molecular sciences
Not labelled yetIdentification of SOD1 Gene Variants in Mexican Patients with Amyotrophic Lateral Sclerosis.International journal of molecular sciences
ReviewNeuromuscular junction pathology in amyotrophic lateral sclerosis and emerging molecular therapeutic strategies.Journal of human genetics
ReviewBeyond Monogenic Inheritance: Emerging Genetic Architecture of Amyotrophic Lateral Sclerosis.International journal of molecular sciences
ReviewSerotonergic Dysfunction and the Interacting Role of TAR DNA-Binding Protein 43 in the Progression of Amyotrophic Lateral Sclerosis: A Scoping Review.Biomolecules
Not labelled yetRespiratory Phenotypes for Stratifying and Predicting Survival in ALS.Muscle & nerve
Not labelled yetRate and Shape of Functional Decline in Amyotrophic Lateral Sclerosis Identify Clinically Distinct Amyotrophic Lateral Sclerosis Phenotypes.Annals of neurology
ReviewTDP-43 dysfunction destabilizes glial homeostatic identity in ALS/FTD.Brain research
Not labelled yetMeta-Analysis of ALS Post-Mortem Cerebral Cortex Transcriptome Studies Identifies Robust Shifts in Gene Expression Despite Significant Between-Study Heterogeneity.Brain sciences
Not labelled yetGlobal best practice recommendations for genetic counselling and testing in amyotrophic lateral sclerosis.Brain : a journal of neurology
Not labelled yetFunctional Status, Quality of Life and Survival After Repeated Intrathecal Administration of Autologous Lineage-Negative Cells in Amyotrophic Lateral Sclerosis.Journal of clinical medicine
Not labelled yetDiaphragm reserve utilisation in motor neurone disease: A novel ultrasound-derived physiological index.Respiratory physiology & neurobiology
Case reportAmyotrophic Lateral Sclerosis in a Patient Treated for Neurosyphilis: A Case Report.Neurology international
Not labelled yetMotor neuron disease and parkinsonism in a patient with a pathogenic CSF1R variant.Revue neurologique
Not labelled yetCost-effectiveness of multidisciplinary care compared with standard neurology care in Amyotrophic Lateral Sclerosis: A model-based cost-utility analysis.Journal of the neurological sciences
Not labelled yetSingle-Dose Intrathecal rAAV2-Retro Delivering Anti-hSOD1 miRNA Confers Robust Neuroprotection in Adult ALS Mice.Cells
Not labelled yetMild cognitive impairment in presymptomatic amyotrophic lateral sclerosis.Journal of neurology
PreprintCCT2 expression marks a translation-activated state in sporadic ALS motor neurons and is associated with functional decline.bioRxiv : the preprint server for biology
Not labelled yetOutcomes of patients with amyotrophic lateral sclerosis admitted to the ICU for acute respiratory failure.Annals of intensive care
Not labelled yetCortical Motor Hierarchy Disruption Is Associated With Functional Status in Early Amyotrophic Lateral Sclerosis.Journal of cachexia, sarcopenia and muscle
Not labelled yetA CNS-targeted atovaquone nanotherapy mitigates complement activation and neuromuscular degeneration in ALS.Materials today. Bio
PreprintSomatic instability of the C9orf72 repeat expansion in blood differs between patients with amyotrophic lateral sclerosis or frontotemporal dementia.medRxiv : the preprint server for health sciences
ReviewThe clinical spectrum of suicide-related outcomes in amyotrophic lateral sclerosis: A systematic review and meta-analysis.General hospital psychiatry
Not labelled yetFeasibility and apparent safety of functional electrical stimulation-assisted cycling in amyotrophic lateral sclerosis and primary lateral sclerosis: a single-arm longitudinal pilot feasibility study.European journal of translational myology
Systematic reviewSelected traditional Chinese medicines for treating amyotrophic lateral sclerosis: a Bayesian network meta-analysis based on randomised controlled trials.Frontiers in pharmacology
Not labelled yetPostsynaptic remodeling and F-actin dysregulation in the Dctn1Δ2-4 mouse model of motor neuron disease.Neural regeneration research
Not labelled yetCerebellar involvement in sporadic amyotrophic lateral sclerosis: a magnetic resonance spectroscopy study.Brain communications
Not labelled yetConstructing functional neural circuits to model amyotrophic lateral sclerosis with induced pluripotent stem cell-derived brain organoids.Neural regeneration research
Not labelled yetRiluzole-Derived Benzo[d]thiazoles as CK1δ Inhibitors for Amyotrophic Lateral Sclerosis-Related Neurodegeneration.ChemMedChem
Not labelled yetTau isoform mapping across tissues and biofluids reveals a signature distinguishing Alzheimer's disease from amyotrophic lateral sclerosis.Nature communications
ReviewState transitions in amyotrophic lateral sclerosis: mechanistic convergence and biomarker-guided stratification.Neuroscience
Case reportCase Report: Herbal nutritional intervention in a critically ill ALS patient with multidrug-resistant infection.Frontiers in medicine
Not labelled yetPlasma Lipidome Is Dysregulated in Amyotrophic Lateral Sclerosis and Associated With Life-Course Adiposity Polygenic Risk.Journal of cachexia, sarcopenia and muscle
Not labelled yetUnderstanding Holistic Patient-Relevant Measurement in Amyotrophic Lateral Sclerosis: A Mixed-Methods Content Validity and Exploratory Rasch Analysis of Selected Clinical Outcome Assessments.Neurology and therapy
Case reportLower Motor Neuron Disease Misclassified As Inflammatory Myopathy in a Young Woman With Myositis-Specific Antibodies.Cureus
Not labelled yetSerum p-tau181 and p-tau217 levels in adolescents and adults with 5q spinal muscular atrophy.Journal of neurology
Not labelled yetEnd-of-life care of patients with amyotrophic lateral sclerosis and home mechanical ventilation: the national population-based DISCOVERY study.Amyotrophic lateral sclerosis & frontotemporal degeneration
Trial resultABCD-Trial: study protocol for a randomized, double-blind, placebo-controlled study in patients with Amyotrophic lateral sclerosis for the evaluation of efficacy and safety of B-Cell Depletion with rituximab (ABCD).Trials
Not labelled yet"It's like saving for a rainy day": perceptions of voice banking for people living with Motor Neurone Disease.Augmentative and alternative communication (Baltimore, Md. : 1985)
Not labelled yetCerebrospinal fluid amyloid and neurodegeneration biomarkers in the diagnosis and prognosis of amyotrophic lateral sclerosis: a multicohort observational study.EBioMedicine
Not labelled yetPlasma Proteomic Signatures Predict Incident Amyotrophic Lateral Sclerosis: A Prospective Study Stratified by C9orf72 Expansion.Journal of cachexia, sarcopenia and muscle
Not labelled yetData-driven progression trajectories across clinical subtypes of amyotrophic lateral sclerosis.Journal of the neurological sciences
Not labelled yetProtein disulphide isomerase protects against ALS/FTD phenotypes associated with cyclin F in zebrafish and cellular models.Redox report : communications in free radical research
Not labelled yetFactors associated with post-tracheostomy survival in Amyotrophic Lateral Sclerosis.Amyotrophic lateral sclerosis & frontotemporal degeneration
Not labelled yetMolecular recognition of axonal injury-associated candidate hub genes and predicted inhibitors across Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis.In silico pharmacology
Not labelled yetOGT regulates RNA-binding protein nucleocytoplasmic partitioning, but this fails in amyotrophic lateral sclerosis.iScience
Not labelled yetPeripheral and cerebrospinal fluid inflammatory markers in sporadic amyotrophic lateral sclerosis an exploratory cross-sectional association study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
ReviewMapping care interventions for people living with motor neurone disease: a living evidence and gap map.Neurodegenerative disease management
Not labelled yetSalivary Dim-Light Melatonin Onset is Associated with Functional Decline, Respiratory Symptom Emergence, and Survival in Early Amyotrophic Lateral Sclerosis.Annals of neurology
ReviewMotor Neuron Disease in a Dish: The Power of Human Induced Pluripotent Stem Cell-Derived Spinal Motor Neurons and Glial Cells.Cells
Not labelled yetPhenotypic Profiling of SOD1-G93A Mice: Integrating Sciatic Nerve Histopathology with Systemic Chemokine Dynamics During ALS Progression.International journal of molecular sciences
Case reportEthical Dilemmas in Predictive Testing for Monozygotic Twins With Hereditary ALS: A Clinical Case Report.Journal of genetic counseling
Not labelled yetSerum neurofilament and measures of lower motor neuron dysfunction in amyotrophic lateral sclerosis.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
Not labelled yetAn integrative transcriptomic atlas of ALS and aging skeletal muscle defines shared and distinct molecular programs of degeneration.Proceedings of the National Academy of Sciences of the United States of America
Not labelled yetNeeds and Expectations of ALS Patients and Caregivers: An Integrated Perspective.European neurology
Not labelled yetCorrigendum to "Exploring the cuproptosis-related molecular clusters in the peripheral blood of patients with amyotrophic lateral sclerosis" [Comput. Biol. Med. 168, (2024), 107776].Computers in biology and medicine
ReviewDiagnostic evolution of carbonic anhydrase 3 (CA3) in Amyotrophic Lateral Sclerosis (ALS): an emerging prognostic biomarker.Expert review of neurotherapeutics
ReviewDNA methylation in motor neuron biology and epigeneticopathy in amyotrophic lateral sclerosis.Handbook of clinical neurology
Not labelled yetBullous Pemphigoid in Patients with Amyotrophic Lateral Sclerosis: A Retrospective Study of 1,067 Cases.Internal medicine (Tokyo, Japan)
Not labelled yetIsolated Axoplasm from Squid and Pathogenic Mechanisms in Amyotrophic Lateral Sclerosis.Journal of visualized experiments : JoVE
ReviewMapping the evidence on dignity therapy in amyotrophic lateral sclerosis: a scoping review.Amyotrophic lateral sclerosis & frontotemporal degeneration
Not labelled yetVascular profiling of the spinal cord and cortex reveals region-specific endothelial dysfunction and fibroblast remodeling in human ALS.Acta neuropathologica communications
Not labelled yetNeurovascular Modulation of the Blood-brain Barrier Using Focused Ultrasound for Antisense Therapy Delivery in Amyotrophic Lateral Sclerosis.Current neurovascular research
Not labelled yetOptimized gGBE enables robust G-to-Y conversion in mammalian cells and zebrafish embryos.Zoological research
Not labelled yetBrain-computer interfaces and neuroprostheses for severe speech impairment in amyotrophic lateral sclerosis.Annals of medicine and surgery (2012)
ReviewRevisiting the muscle spindle in ALS: Implications for spinal motor network dysfunction.Pflugers Archiv : European journal of physiology
Not labelled yetAssessing the metabolic rate in patients with Amyotrophic Lateral Sclerosis, Progressive Muscular Atrophy, and Primary Lateral Sclerosis.Amyotrophic lateral sclerosis & frontotemporal degeneration
Not labelled yetIntegrative ALS therapy: gene targeted therapy by base editing and potential exercise rehabilitation as synergistic strategies for functional recovery.Physical activity and nutrition
Not labelled yetStatin Exposure and Survival Outcomes in Amyotrophic Lateral Sclerosis in an Asian Cohort.Muscle & nerve
Not labelled yetTranscutaneous Carbon Dioxide Monitoring in Amyotrophic Lateral Sclerosis: A Scoping Review.European journal of neurology
Not labelled yet[Effect of electroacupuncture at Jiaji (EX-B2) on disease progression in mice with amyotrophic lateral sclerosis based on NLRP3/Caspase-1/ASC signaling pathway].Zhongguo zhen jiu = Chinese acupuncture & moxibustion
Not labelled yetMapping high resolution, multidimensional phase diagrams of near-physiological protein condensates.Nature communications
ReviewHistory of Head Injury and Risk of Amyotrophic Lateral Sclerosis: An Updated Comprehensive Systematic Review with Meta-Analysis of 5,033,215 Participants.Neuroepidemiology
Not labelled yetCombined rituximab and magnesium acetyl taurate therapy attenuates neurodegeneration via ERK/c-JNK/P38MAPK signaling modulation in methylmercury-induced amyotrophic lateral sclerosis-like neurotoxicity.Naunyn-Schmiedeberg's archives of pharmacology
Not labelled yetSigma-1 Receptor Mitigates Poly-GR-Associated Redox Dysregulation by Restoring NRF2/HO1 Signaling in C9orf72-Associated ALS.Neuromolecular medicine
PreprintAll Roads Lead to Rome: Resting-State Criticality as a Neurophysiological Marker of Brain-Computer Interface (BCI) Performance in People with Amyotrophic Lateral Sclerosis (ALS) and Healthy Participants.Research square
Review[The role of the GSTP1/JNK signaling pathway in regulating oxidative stress and programmed cell death in amyotrophic lateral sclerosis].Zhonghua nei ke za zhi
PreprintALS/FTD-linked TDP-43 alterations prevent HSV-1 infection by disrupting cell-adhesion pathways.bioRxiv : the preprint server for biology
ReviewPrognostication in Amyotrophic Lateral Sclerosis: A Narrative Review of Pre-Diagnosis and Functional Outcomes.NeuroRehabilitation
Not labelled yetLateral sclerosis in amyotrophic lateral sclerosis is an upper motor neuron distal axonopathy ("dying back"): a clinical-neuropathological study.Acta neuropathologica
ReviewMinding the gates: dual cell-autonomous and non-cell-autonomous mechanisms of TBK1 in ALS/FTD.Frontiers in neuroscience
Not labelled yetNeurofilaments support the differentiation of amyotrophic lateral sclerosis from degenerative cervical myelopathy.Journal of neural transmission (Vienna, Austria : 1996)
ReviewComparison between ultrasound and electromyography for detection of fasciculations in amyotrophic lateral sclerosis: an updated systematic review and meta-analysis.Radiologia brasileira
Not labelled yetCorrigendum to "The Values and Preferences of People Living With Motor Neurone Disease (MND): A Systematic Review and Meta-Analysis".Clinical and public health guidelines
Not labelled yetMultiple motor proteins regulate TDP-43 anterograde axonal transport.Acta neuropathologica
Not labelled yetEARLY-ALS: a multicentre study on prodromal amyotrophic lateral sclerosis.EBioMedicine
Not labelled yetAnti-HDGFL2 cryptic protein antibodies provide a sensitive readout of TDP-43 pathology and clinical disease features.Cell reports. Medicine
Not labelled yetPlasma cardiac troponin T as a marker of skeletal muscle involvement in amyotrophic lateral sclerosis.Brain communications
ReviewTraditional Chinese botanical medicines and plant-derived bioactive compounds in amyotrophic lateral sclerosis: mechanistic evidence, translational challenges, and therapeutic opportunities.Frontiers in pharmacology
Not labelled yetWhite matter hyperintensity burden in amyotrophic lateral sclerosis: motor and survival correlates.Brain : a journal of neurology
Review[Amyotrophic lateral sclerosis: Specific considerations in palliative care].MMW Fortschritte der Medizin
Not labelled yetPre-diagnostic ALSFRS-R slope provides limited incremental information about the variability in subsequent functional decline in amyotrophic lateral sclerosis: a population-based study.Journal of neurology
Not labelled yetEarly Palliative Care and Structured Serious Illness Communication in a Refugee Patient With Amyotrophic Lateral Sclerosis.The primary care companion for CNS disorders
Not labelled yetCorrection: Feasibility study of noninvasive assessment of emotional state in patients with ALS.Frontiers in digital health
Case reportContrasting clinical trajectories in two ALS patients with rare FUS variants: implications for variant interpretation, penetrance, and trial readiness.Neurogenetics
Not labelled yetGenetic testing and counselling of patients with monogenic amyotrophic lateral sclerosis in Northern Finland: a retrospective, single-centre study.European journal of human genetics : EJHG
Not labelled yetImmune effects of faecal microbiota transplantation in amyotrophic lateral sclerosis: a pilot multicentre, randomised, masked, sham-controlled, proof-of concept trial.EBioMedicine
Not labelled yetOne-Year Clinical Course of Patients With Amyotrophic Lateral Sclerosis Admitted to a Home Palliative Care Program: An Extension Study.Muscle & nerve
Not labelled yetClinical and genetic characterization of FUS-associated ALS in a tertiary cohort.Amyotrophic lateral sclerosis & frontotemporal degeneration
Not labelled yetN-terminal proVGF modifications related to Amyotrophic Lateral Sclerosis.Amyotrophic lateral sclerosis & frontotemporal degeneration
Not labelled yetRecalibration of the Frontal Behavioural Inventory Cut-Off for Behavioural Screening in Amyotrophic Lateral Sclerosis.European journal of neurology
Not labelled yetNanopore sequencing combined with adaptive sampling and NanoExpansion enables accurate characterization of repeat expansion disorders.NAR genomics and bioinformatics
Not labelled yetAstrocytes regulate axonal mitochondrial transport deficits in C9ORF72 amyotrophic lateral sclerosis motor neurons.Nature neuroscience
Case reportFooled by the Heartbeat: Cardioballistic Autotriggering in Amyotrophic Lateral Sclerosis.Archivos de bronconeumologia
Randomised trialTRICALS risk score augments but cannot replace neurofilament as a prognostic biomarker in ALS.Journal of neurology
Not labelled yetBridging stakeholder needs and technological capabilities to identify humanoid robot applications in rehabilitation: a case study in an ALS multidisciplinary care unit.Frontiers in robotics and AI
ReviewSOD1 co-pathologies in the brain: insights from neuropathological evidence and implications.Acta neuropathologica
Not labelled yetNeuroimaging signatures of facial onset sensory and motor neuronopathy (FOSMN).Journal of neurology
Case reportWhen Hypercapnia Misleads: A Case of Respiratory-Onset Motor Neuron Disease.Cureus
Not labelled yetEnzymatic N-deacylation is the predicted membrane-disruption switch for sphingomyelin: a falsifiable in-silico framework for sphingolipid vulnerability in ALS.Journal of molecular graphics & modelling
Not labelled yetMultisite Anodal Direct Current Stimulation Preserves Motor Function and Modulates Key Cellular Pathways in TDP-43 and SOD1 Mouse Models of Amyotrophic Lateral Sclerosis.Neuromodulation : journal of the International Neuromodulation Society
Not labelled yetTBK1 eliminates aggregation-prone monomeric TDP-43 through an IFNβ-immunoproteasome pathway in ALS models.EMBO reports
Not labelled yetDecoupling metabolic defense: Mutational and recombinational chaos in Sod1-deficient cells.PLoS genetics
ReviewTDP-43 and ALS - what's wrong with my membranes?Neurobiology of disease
Case reportWhen the Electromyography (EMG) and the Patient Disagree: Unraveling a Motor Neuron Disease Mimic With Small-Fiber Dysfunction.Cureus
Not labelled yetCerebrospinal fluid inflammatory proteomic profiling identifies biomarkers linked to disease progression in amyotrophic lateral sclerosis.Journal of neurology
Not labelled yetMdivi-1 regulates mitochondrial fission and function via the CaMK2/Drp1 pathway in amyotrophic lateral sclerosis.Neuroscience
Case reportAmyotrophic Lateral Sclerosis.Continuum (Minneapolis, Minn.)
Not labelled yetAssociations Between Prediagnosis Plasma Neurofilament Light Polypeptide and Amyotrophic Lateral Sclerosis Risk in the Danish EPIC Cohort.Annals of neurology
Not labelled yetNitrate-responsive Sialin2 couples stress granule assembly and clearance to maintain neuronal homeostasis.Developmental cell
Not labelled yetThe accessory makes the drug: ASO-delivered siRNA enters the human CNS for ALS.Cell stem cell
PreprintClonal CD8 T cells link peripheral and intrathecal immunity in ALS4 progression: a multiomics reference for ALS.Research square
Not labelled yetInsertion or deletion variants in TAF15 exon 15 are genetic factors impacting the prognosis of amyotrophic lateral sclerosis in a Japanese cohort.European journal of human genetics : EJHG
Not labelled yetA genetic screen for suppressors of neuron degeneration in a C. elegans sod-1G85R model of Amyotrophic Lateral Sclerosis.G3 (Bethesda, Md.)
Not labelled yetNear-optimal P300 speller performance using large language models: A multi-model analysis with performance bounds.PloS one
Not labelled yetCore and bridge nodes between sleep quality and depression in Chinese patients with amyotrophic lateral sclerosis: A network analysis perspective.General hospital psychiatry
Not labelled yetPredictive value of the modified controlling nutritional status score for critical events in patients with amyotrophic lateral sclerosis.Clinical nutrition ESPEN
Not labelled yetDevelopment of Antisense Oligonucleotide Gapmers for Amyotrophic Lateral Sclerosis.Methods in molecular biology (Clifton, N.J.)
Not labelled yetCaregiving and Respite for People With Motor Neurone Disease: A National Cross-Sectional Survey of Experiences and Challenges.Journal of clinical nursing
Not labelled yetAnesthetic Management and Perioperative Outcome of Emergency Laparotomy in a Patient With Advanced Motor Neurone Disease: A Case Report.Clinical case reports
Not labelled yetMotor dysfunction phenotypes in a drosophila model validate DAO as an ALS gene.Human molecular genetics
Not labelled yetResponse to: Comment on 'The Values and Preferences of People Living With Motor Neurone Disease (MND): A Systematic Review and Meta-Analysis'.Clinical and public health guidelines
Not labelled yetAcute viral infection accelerates neurodegeneration in a mouse model of ALS.Nature communications
Not labelled yet[What to learn and teach to implement Shared Care Planning for people with Amyotrophic Lateral Sclerosis? Nominal Group Technique].Revista de la Facultad de Ciencias Medicas (Cordoba, Argentina)
Not labelled yetComment on 'The Values and Preferences of People Living With Motor Neurone Disease (MND): A Systematic Review and Meta-Analysis'.Clinical and public health guidelines
Not labelled yetConformational insights into the unfolding pathway of RNA recognition motif (RRM) domain of TAF15 associated with amyotrophic lateral sclerosis.Journal of biomolecular structure & dynamics
Not labelled yetLRSAM1, an E3 ubiquitin ligase, modulates TDP-43 proteostasis in amyotrophic lateral sclerosis.Brain : a journal of neurology
Not labelled yetREM-associated nocturnal hypercapnia in amyotrophic lateral sclerosis.QJM : monthly journal of the Association of Physicians
ReviewInsights into X-linked Dystonia-Parkinsonism and Spinocerebellar Ataxia type 36 Through the Lens of Amyotrophic Lateral Sclerosis/Frontotemporal Dementia.Molecular neurobiology
Not labelled yetBatch- and Composition-Controlled Reanalysis of Bulk and Single-Nucleus Transcriptomes Reveals Co-Enrichment of Glial Complement and of Translational Signatures in Parkinson's Disease and Amyotrophic Lateral Sclerosis.International journal of molecular sciences
Not labelled yetEffects of Dietary Supplementation with Conjugated Linoleic Acid on Redox Marker Profiles and Neuroaxonal Degeneration in Amyotrophic Lateral Sclerosis.Antioxidants (Basel, Switzerland)
Not labelled yetMitochondrial Quality Control Impairment Is a Hallmark of TDP-43G376D ALS Patient-Derived Fibroblasts.Antioxidants (Basel, Switzerland)