What researchers published on ALS (motor neurone disease)
2,064 papers, newest first.
Showing 60 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