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What researchers published on ALS (motor neurone disease)

2,064 papers, newest first.

Showing 120 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)